Wednesday 22 May 2013

Websense to go private after years of slow growth

(Reuters) - Websense Inc said it had agreed to be taken private by Vista Equity Partners in a deal that values the online security firm at about $907 million, a move that should come as a relief to investors after years of weak sales from its legacy business.

The offer of $24.75 per share represents a roughly 29 percent premium to Websense's Friday close. Websense shares rose to just above the offer price to a near two-year high in morning trading on the Nasdaq.

"After years of speculation, investors will be rubbing their eyes this morning that Websense finally got acquired and will go the route of other security software vendors that got the private equity bid," FBR Capital analyst Daniel Ives said.

The company joins a list of security software vendors, including Blue Coat that was bought by Thoma Bravo in 2011, to get private equity bids.

The company's growth rate has slowed in the past few years as its core web filtering business weakened and it reported a slight revenue decline last year.

Websense stock, which peaked at $34.87 in 2005, has since fallen 22 percent until Friday's close.

"This morning's acquisition speaks to the value of security software ... a surge of M&A activity is poised to hit the sector over the next six to 12 months as larger technology players and private equity look to get a larger piece of the security pie," he said.

Ives added that the acquisition would allow Websense to focus on its promising Triton business that makes web security gateway and e-mail security products.

Websense, which said it expected the deal to close before the end of the third quarter, said its senior management was expected to continue with the company and its headquarters would remain in San Diego.

BofA Merrill Lynch is the financial adviser to Websense and Cooley LLP its legal adviser.

Kirkland & Ellis LLP is Vista's legal adviser and J.P. Morgan Securities, RBC Capital Markets and Guggenheim Partners have agreed to provide debt financing for the deal.

Vista Equity is a private equity firm that invests primarily in software companies and has about $6 billion in assets.

(Reporting by Sayantani Ghosh in Bangalore; Editing by Roshni Menon and Don Sebastian)

Source: http://news.yahoo.com/websense-private-907-million-124705624.html

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Source: http://www.nuhitz.com/blog/41506/low-budget-travel-insurance-in-which-way-to-find-typically-the-most-suitabl/

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Tuesday 21 May 2013

What Your Sunscreen Should?and Shouldn't?Have

First and foremost, spring and summer mean sun. We all know that we need some of it (sunshine enables our body to absorb vitamin D, which is essential for bone density and a strong immune system), but there?s also the sun?s not-so-healthy aspect: skin cancer. Since 1975, rates of melanoma?the deadliest kind of skin cancer?have tripled, reaching nearly one-quarter of the population, according to the National Cancer Institute (NCI). Adolescents and young adults have been particularly hard hit, with the rate of the cancer among teens growing at a rate of 2 percent per year between 1973 and 2009, according to one 2013 study. Using a tanning bed and as little as one bad sunburn can dramatically increase your lifetime risk.

Fortunately, a good sunscreen can be a help.? (The best defense against skin cancer, though, is still avoiding the sun, especially during the peak hours of 10 AM to 2 PM.) But for the times you do need or want to be outside, how do you choose a good sunscreen? The Environmental Working Group (EWG) has made that task easier with its just-released ?EWG?s 2013 Guide to Sunscreens.? Unlike a lot of other ?best of? roundups, this list of top-rated sunscreens and related products?it includes moisturizers, lip balms, and make-up?not only features products that work to protect you against some damaging UV rays, but the best of these products?the ones that have earned the EWG?s lowest ratings?are also low in harmful chemicals.?

?

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One of the lines featured in three out of four of the EWG?s categories is Ava Anderson NonToxic, a line of 122 personal care products and cosmetics developed by 19-year-old Ava Anderson. When she launched in 2009 with her mom, Kim, then-15-year-old Ava wanted to create products that really worked, but without toxic ingredients. Her inspiration? Mother and daughter had watched a news segment highlighting an EWG study of chemicals found in teenagers. ?Every teen tested positive for every ingredient,? says Ava. ?We were both shocked,? Kim remembers.

After seeing the news report, Ava went to a local drugstore and health food store figuring that, as she says, ?I could buy my way out of this. But then I started researching ingredients.? Her research went on for the better part of a year; when she was done, she told her parents, ?I?m not satisfied with what?s available. I want to start my own line of non-toxic products.?

Ava now hosts house parties sponsored by her brand to help people learn about toxins and to sample and buy healthy non-toxic products at reduced cost. Ava and Kim have also made numerous trips to Capitol Hill to educate legislators on the toxins in personal care products, which are neither regulated nor adequately tested for their health effects. ?Most people, even Congresspeople, have no idea of the chemicals we are exposed to and their risks to our health,? Kim says. If it?s passed, the Safe Cosmetics and Personal Care Products Act of 2013 will introduce these protections for the first time.

If it's passed, the Safe Cosmetics and Personal Care Products Act of 2013 would help make clear to consumers which harmful chemicals are in the products we use.

When it comes to choosing healthy sun-care products, it helps to have a bit of information about what?s in these products so you can purchase wisely. ?First, both traditional sunscreen and other products with SPF contain many of the same questionable chemicals found in other personal care and cosmetic products, such as parabens (which are carcinogenic) and retinyl palmitate (which actually increases sun sensitivity, yet is used in many products). The active ingredients in sunscreens are either minerals?principally titanium or zinc oxide?or chemicals like oxybenzone and oxtinoxate, which are endocrine (hormone) disruptors that ?are toxic to reproductive systems or interfere with normal development,? EWG researchers found. Choosing products with a score of two or less on the EWG?s Guide to Sunscreens will help you avoid them. The lower the number on the EWG?s list, the less toxic the product; all of Ava?s products are rated by EWG as a ?one,? for non-toxic, and are available on her website.

It?s important to understand, too, that many sunscreen products simply don?t do the job. The Food & Drug Administration (FDA) has only approved a few of the many effective chemical ingredients that are available in sunscreens in other countries, and the formulations used in the U.S. don?t actually screen skin-damaging UVA rays. Nevertheless, the FDA allows product manufacturers to market their products with claims that they provide ?broad spectrum? coverage?even though they do not contain ingredients that screen UVA radiation effectively. Simply put, American sunscreens are weaker.

Yet instead of avoiding the sun, people use them believing that they are protected. A high SPF number does not guarantee protection. In fact, Ava warns that, ?it may mislead you into baking longer believing you are safe, when you aren?t.? Also, higher numbers aren't better: An SPF of 30 is as effective as a supposedly higher SPF if you reapply it as the label suggests.

And for true UVA protection, higher molecule-sized zinc oxide is the most effective sunscreen ingredient. Zinc oxide?s ghost-white appearance in sunscreen may make you look like a lifeguard, but most products are now formulated so that they're a barrier to the sun without giving you that chalky look. Ava?s line, and some other on EWG's new list, have it, while also omitting harmful ingredients that increase sun sensitivity. While none of the products will protect you if you bake in the sun during the hours of highest UV radiation, they will help to minimize exposure. Sun avoidance remains the best protection.

If you want to do more to ensure that cosmetic and beauty products are better studied, formulated, and regulated for safety, Ava and Kim suggest going to the Campaign for Safer Cosmetics, as well as the EWG?s site.

Here?s how to find the product you?re looking for on the EWG?s new list of top-rated sunscreens and sun-protection products:

Beach and Sport Sunscreens (184 products meet the EWG?s criteria)

Moisturizers with SPF (22 products meet the EWG?s criteria)

Lip Balms with SPF (18 products meet the EWG?s criteria)

Make Up with SPF (16 products meet the EWG?s criteria)

What?s your favorite sunscreen? What chemicals do you avoid in personal care and cosmetic products?

Related Stories on TakePart:

??Even a Deadly Skin Cancer Doesn?t Stop Some From Tanning

??Are Your ?Natural? Beauty Products Really Natural?

??More Coffee, Less Skin Cancer Risk

Alison Rose Levy has covered health, food, and the environment on Huffington Post, AlterNet, PsychologyToday, and Intent.com. The writer of two best-selling health books, Alison talks to health and eco leaders on her weekly radio program, Connect the Dots on the Progressive Radio Network.?@alisonroselevy | TakePart.com

Source: http://news.yahoo.com/sunscreen-shouldnt-170930959.html

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UofL scientists uncover how grapefruits provide a secret weapon in medical drug delivery

UofL scientists uncover how grapefruits provide a secret weapon in medical drug delivery [ Back to EurekAlert! ] Public release date: 21-May-2013
[ | E-mail | Share Share ]

Contact: Julie Heflin
julie.heflin@louisville.edu
502-852-7987
University of Louisville

LOUISVILLE, Ky. Grapefruits have long been known for their health benefits, and the subtropical fruit may revolutionize how medical therapies like anti-cancer drugs are delivered to specific tumor cells.

University of Louisville researchers have uncovered how to create nanoparticles using natural lipids derived from grapefruit, and have discovered how to use them as drug delivery vehicles. UofL scientists Huang-Ge Zhang, D.V.M., Ph.D., Qilong Wang, Ph.D., and their team today (May 21, 2013), published their findings in Nature Communications.

"These nanoparticles, which we've named grapefruit-derived nanovectors (GNVs), are derived from an edible plant, and we believe they are less toxic for patients, result in less biohazardous waste for the environment, and are much cheaper to produce at large scale than nanoparticles made from synthetic materials," Zhang said.

The researchers demonstrated that GNVs can transport various therapeutic agents, including anti-cancer drugs, DNA/RNA and proteins such as antibodies. Treatment of animals with GNVs seemed to cause less adverse effects than treatment with drugs encapsulated in synthetic lipids.

"Our GNVs can be modified to target specific cells we can use them like missiles to carry a variety of therapeutic agents for the purpose of destroying diseased cells," he said. "Furthermore, we can do this at an affordable price."

The therapeutic potential of grapefruit derived nanoparticles was further validated through a Phase 1 clinical trial for treatment of colon cancer patients. So far, researchers have observed no toxicity in the patients who orally took the anti-inflammatory agent curcumin encapsulated in grapefruit nanoparticles.

The UofL scientists also plan to test whether this technology can be applied in the treatment of inflammation related autoimmune diseases like rheumatoid arthritis.

A Common Sense Approach

Zhang said he began this research by considering how our ancestors selected food to eat.

"The fruits and vegetables we buy from the grocery today were passed down from generation to generation as favorable and nutritious for the human body. On the flip side, outcomes were not favorable for our ancestors who ate poisonous mushrooms, for example," he said. "It made sense for us to consider eatable plants as a mechanism to create medical nanoparticles as a potential non-toxic therapeutic delivery vehicle."

In addition to grapefruit, Zhang and his team analyzed the nanoparticles from tomatoes and grapes. Grapefruits were chosen for further exploration because a larger quantity of lipids can be derived from this fruit.

###


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?


AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert! system.


UofL scientists uncover how grapefruits provide a secret weapon in medical drug delivery [ Back to EurekAlert! ] Public release date: 21-May-2013
[ | E-mail | Share Share ]

Contact: Julie Heflin
julie.heflin@louisville.edu
502-852-7987
University of Louisville

LOUISVILLE, Ky. Grapefruits have long been known for their health benefits, and the subtropical fruit may revolutionize how medical therapies like anti-cancer drugs are delivered to specific tumor cells.

University of Louisville researchers have uncovered how to create nanoparticles using natural lipids derived from grapefruit, and have discovered how to use them as drug delivery vehicles. UofL scientists Huang-Ge Zhang, D.V.M., Ph.D., Qilong Wang, Ph.D., and their team today (May 21, 2013), published their findings in Nature Communications.

"These nanoparticles, which we've named grapefruit-derived nanovectors (GNVs), are derived from an edible plant, and we believe they are less toxic for patients, result in less biohazardous waste for the environment, and are much cheaper to produce at large scale than nanoparticles made from synthetic materials," Zhang said.

The researchers demonstrated that GNVs can transport various therapeutic agents, including anti-cancer drugs, DNA/RNA and proteins such as antibodies. Treatment of animals with GNVs seemed to cause less adverse effects than treatment with drugs encapsulated in synthetic lipids.

"Our GNVs can be modified to target specific cells we can use them like missiles to carry a variety of therapeutic agents for the purpose of destroying diseased cells," he said. "Furthermore, we can do this at an affordable price."

The therapeutic potential of grapefruit derived nanoparticles was further validated through a Phase 1 clinical trial for treatment of colon cancer patients. So far, researchers have observed no toxicity in the patients who orally took the anti-inflammatory agent curcumin encapsulated in grapefruit nanoparticles.

The UofL scientists also plan to test whether this technology can be applied in the treatment of inflammation related autoimmune diseases like rheumatoid arthritis.

A Common Sense Approach

Zhang said he began this research by considering how our ancestors selected food to eat.

"The fruits and vegetables we buy from the grocery today were passed down from generation to generation as favorable and nutritious for the human body. On the flip side, outcomes were not favorable for our ancestors who ate poisonous mushrooms, for example," he said. "It made sense for us to consider eatable plants as a mechanism to create medical nanoparticles as a potential non-toxic therapeutic delivery vehicle."

In addition to grapefruit, Zhang and his team analyzed the nanoparticles from tomatoes and grapes. Grapefruits were chosen for further exploration because a larger quantity of lipids can be derived from this fruit.

###


[ Back to EurekAlert! ] [ | E-mail | Share Share ]

?


AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert! system.


Source: http://www.eurekalert.org/pub_releases/2013-05/uol-usu052113.php

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DOJ Goes After Fox News Reporter (ABC News)

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Robert Pattinson and Kristen Stewart Split: What Went Wrong?

Source: http://www.thehollywoodgossip.com/2013/05/robert-pattinson-and-kristen-stewart-split-what-went-wrong/

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One man's escape from Camp 14 and North Korea

Only one prisoner born in North Korea's gulag is known to have escaped to tell his story. A Q&A with Blaine Harden, the journalist who wrote about Shin Dong-hyuk.

By Robert Marquand,?Staff writer / May 21, 2013

Shin Dong-hyuk (seated, l.) was born in a notorious North Korean prison camp, from which he escaped. He?s shown being interviewed on French TV last year.

Blaine Harden

Enlarge

There is only one prisoner actually born in one of North Korea's infamous prison camps known to have escaped alive. His name is Shin Dong-hyuk.

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Mr. Shin was raised in Camp 14, reported to be one of the cruelest in a system of hard labor prisons.

His parents didn't know each other before their brief conjugal marriage arranged by guards. Shin grew up with no idea of a world other than the beatings, torture, and snitching that were part of everyday life at the camp. He betrayed his mother and brother over a meal of rice, sending them to their execution, saw his father as an acquaintance, and roasted rats to stay alive. Yet he also was able to catch his first glimpse of life outside the camp's fence through the unexpected, simple kindness of a fellow inmate.

Shin made his improbable escape at age 23 in search of food; if caught he faced execution. But after a harrowing trip to China, he made it to Seoul, South Korea.

Washington Post correspondent Blaine Harden's book "Escape from Camp 14" has made Shin the best-known advocate for exposing the North's hidden prisons. Former Secretary of State Hillary Rodham Clinton mentioned Shin at the Holocaust Memorial Museum in Washington.

Mr. Harden spoke with the Monitor in late April.

(Read the Monitor's article about the new UN inquiry into North Korea's gulag system)

Are these like the camps in Nazi Germany?

No, these are not death camps; the authorities do not execute people as a matter of course. They work people to death, but that happens over a number of years.

Probably a better analogy is Stalin's Gulag. The camps were set up under Kim Il-sung, an acolyte of Stalin, as a mirror of the Soviet Gulag. What is different in the North Korean case is that they seem to be crueler and have lasted twice as long.

Camp 14 has a reputation for housing high-level Pyongyang people that run afoul of the regime. It is a completely no-exit camp, with no rehabilitation; guards treat it as a military front line. There is less sleep, more work, more brutality.

Shin is born in a dark place, a product of the camp. But this doesn't last forever?

Yes, he speaks of an awakening. He had the first inklings of it after his mother's execution. He was 14 and in an underground prison with a man who was kind to him, treated his wounds after he was tortured. The kindness of that man, "Uncle," was something to him utterly new. The guy shared his food. He basically lavished attention and love on Shin in a way he had never experienced. So when he got out, went back to normal camp life, got pushed and bullied, it hit him hard. He went into a funk. He said he started to see the camp for what it was, just a really miserable, filthy, stinking place.

Tell us about Shin's turning point after meeting an educated prisoner named Park.

Shin is assigned to snitch on Park but in the end didn't do it. Park starts telling him stories. At one point Park asks where Shin is from. Shin says, "I am from here." Park tells him, "I am from Pyongyang, the capital." Shin had never heard of the place.

But instead of laughing at this ignorant young kid, Park gave him a primer on what it means to be a citizen of the planet, he talked and talked. Before that it never occurred to Shin that people lived outside the fence.

But talk of grilled meat finally got Shin's attention. He started to dream about food, got a spring in his step, and surprised himself by asking Park to escape with him. Shin was interested in finding his next meal, above all. His focus as a feral creature of the camp was self-preservation and maximizing calories. That was everything, the essence of his escape. He wasn't after the bill of rights.

What is Shin like?

He's really smart. It has also been a bumpy ride. But he has friends he trusts now.

He's kind of a jokester, not adolescent, but gets real joy being with friends, especially when they are all eating dinner together.

He pulled out a huge Galaxy phone the last time I saw him. Smart phones are no more recent to him than the concept of friendship or of love. They are both part of this new existence, and I think he has an easier time with technology than with human emotions.

But he seems to know his role is to tell the world through his life what is going on in these camps right now, and the kind of kids they are raising there.

We have had public satellite images of the camps for more than a decade. Where is the outcry?

Three main things have occluded our vision of the human rights catastrophe:

No. 1, by far, is the comic element of the regime. Particularly Kim Jong-il, his appearance, his puffy hair, big glasses, and funny suit. Jon Stewart and "The Daily Show" highlight the risible nature of the images coming out of the North's propaganda machine. It is fun and funny, silly and ridiculous, over the top. It is so funny that it takes up all the oxygen in our perceiving of North Korea. No. 2 and 3 are the nukes and missiles.

Source: http://rss.csmonitor.com/~r/feeds/csm/~3/thsBbCKdMtg/One-man-s-escape-from-Camp-14-and-North-Korea

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Play of the Day: Rounding Up a Tough Week for the White House

With three scandals dogging Barack Obama, the president and government functions continue to be a focal point on late-night television. David Letterman went headlong into the jokes, opening with a connection to the 40th anniversary of the Watergate hearings. He also brought baseball, the Republican party and Joe Biden into the mix.

The Tonight Show's Jay Leno hit similar notes, comparing Obama to Richard Nixon and suggesting that the president might call up Leno guest Mitt Romney and offer him the job.

Saturday Night Live presented its season finale with a surprise Weekend Update appearance by former anchor -- and TV good government supporter -- Amy Poehler to rehash "Really!?! with Seth and Amy." The segment picked apart the IRS, the Tea Party and Obama.

Fast forward to 4:20 to see why the IRS is on edge this time of the year.

?

Source: http://news.yahoo.com/play-day-rounding-tough-week-white-house-120731476.html

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Spaghetti Al Cavolo Nero (Spaghetti with Black Kale) [Recipe ...

May 20, 2013 | 9:00 am

Posted by?Elana Horwich


Photo

Though kale is more commonly known as a staple of the California vegan hippy diet, the darker, flat leaf variety is actually a favorite ingredient unique to Tuscan cooking. If used properly, it will transport you to the rolling countryside of Siena, as this recipe does. However, when I make it with good brown rice pasta, I can invite both my discerning Italian friends and my picky health-nut peeps over to the same dinner party. Everybody is happy and feels they rubbed off on me well.

Ingredients:?(for 4 people)

- 1 bunch lacinato or dinosaur kale (dark flat leaf, not the curly one)

-?extra virgin olive oil - about 1/4 cup?(*Watch video on how to choose the best olive oil.)

- 2 cloves garlic

- 1 large anchovy fillet, preserved in salt or oil (buy here)

- 1 pinch red pepper flakes

- 1 bigger pinch salt plus more for pasta water

- ? ladle of water from pasta pot, plus more if needed to ?bathe? kale

-?parmigiano reggiano and/or pecorino romano (*Watch video: Meal and a Spiel on Parmigiano Reggiano)

- fresh ground black pepper

- 1 pound Italian semolina pasta or gluten-free brown rice pasta (Tinkyada - buy here)

?

1. Put a 6 qt pot of water on stove and cover.

2. Wash the kale and cut off the thick bottom part of the bunch - the bottom 4 inches at least.

3. Slice the rest of the bunch thinly, about 1/4 inch thick or so, and then cut the whole thing in half down the center so each piece is only half as long.

4. Cut the anchovy into tiny bits and set aside.

5. Set a heavy skillet over medium high heat and while it gets hot prepare the garlic.

6. Take the side of kitchen knife and smash the garlic down on a cutting board until the clove splits a bit and the skin is easy to peel off.

7. Pour enough olive oil to cover base of skillet, about 1/4 cup, and drop in the garlic and red pepper flakes. Notice as the garlic lightly bubbles?it is infusing the olive oil with its flavor. (Make sure it does not burn, as this will add a bitter flavor to your whole dish.)

8. Add the anchovy to the pan, stirring it so it dissolves in the oil.

9. Just as the garlic begins to become translucent and slightly golden brown, toss the kale into the oil and toss it, with tongs if you have them, until it is all coated in the oil.

10. Let the kale saute for a minute and then add the salt and a half a ladle of water, turn heat to low and cover.

11. Cook for about 20 minutes or until kale is very dark and very soft, falling apart in your mouth when you taste it, checking on it every so often to make sure it does not burn. If it looks dry add a bit more water.

12. Cook pasta al dente and strain. (Rules for an Al Dente Pasta)

13. Immediately add pasta to the skillet with the kale, turning up heat to a fuoco vivace, a lively flame, medium high. Toss the pasta using pasta tongs (buy here) or two forks until all the spaghetti have been mixed into the ?sauce.?

14. Divide onto plates, generously grate parmigiano and/or pecorino romano and freshly ground pepper on each one.

15. A tavola, to the table!

Watch video on how to cook perfect al dente pasta.

If you live in LA and would like to take cooking classes with Elana, please visit mealandaspiel.com.

We welcome your feedback.

Your information will not be shared or sold without your consent. Get all the details.

JewishJournal.com reserves the right to use your comment in our weekly print publication.

Source: http://www.jewishjournal.com/meal_and_a_spiel/item/spaghetti_al_cavolo_nero_spaghetti_with_black_kale

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Photos of a new Samsung Galaxy S 4 emerge, could it be the Active?

Photos of a new Samsung GS 4 emerge, could it be the Acitve

A stock GS4 may look virtually indistinguishable from its predecessor, but it looks like Samsung's got a new variant of its flagship phone that'll bring it some much-needed visual flair. The folks at GSM Arena unearthed photos of a GT-I9295 model (allegedly called the GS4 Active) sporting a bright red shell with black inserts at the top and bottom and a trio of physical buttons on its chin. If the results returned by the AnTuTu benchmark are to be believed, the phone's equipped with standard GS4 fixins: a quad-core CPU clocked at 1.9Ghz and an Adreno 320 GPU (aka, a Snapdragon 600 SoC) and a 1920 x 1080 display. Naturally, there's no word on pricing, carrier support or an arrival date, but there are a couple more photos of the handset at the source.

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Source: GSM Arena

Source: http://feeds.engadget.com/~r/weblogsinc/engadget/~3/IwMEMs6ziik/

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Monday 20 May 2013

Angelina Jolie, radical strategies for cancer prevention, and genetics

I had been debating whether to blog about Angelina Jolie?s announcement last week in a New York Times editorial entitled My Medical Choice that she had undergone bilateral prophylactic mastectomy because she had been discovered to have a mutation in the BRCA1 gene that is associated with a very high risk of breast cancer. On the one hand, it is my area of expertise and was a big news story. On the other hand, it?s been nearly a week since she announced her decision, and the news story is no longer as topical as it was. Also, I?ve already written about it a couple of times on my not-so-super-secret other blog, making the division of blogging?problematic. So, if some of this is a bit repetitive to those who are also fans of my more?shall we say??insolent persona, I apologize, but try to be patient. I will be doing more than just rehashing a couple of posts from last week (although there will unavoidably be at least a little of that), because there have been even more examples of reactions to Jolie?s announcement that provide what I like to consider ?teachable moments.? I will start by asserting quite bluntly that in my medical opinion, from the information I have available, Angelina Jolie made a rational, science-based decision. How she went about the actual mechanics might have had some less than scientific glitches along the way (more about that later), but the basic decision to remove both of her breasts to prevent breast cancer associated with a BRCA1 mutation that she carried was quite reasonable and very defensible from a scientific standpoint.

One advantage of waiting nearly a week to write about this story is that it provided me with the opportunity to sit back and observe the reactions that Jolie?s decision provoked. One thing that I really didn?t expect (although in retrospect maybe I should have) is the pure denialism on display that genes have any effect whatsoever on cancer. I say ?in retrospect I should have? because I?ve written at least a couple of times before about how quacks use and abuse the term ?epigenetics? in the same way that they abuse the word ?quantum? and how they seem to believe that wishing makes it so (through epigenetics, of course!) to the point where they believe that genetics is irrelevant to cancer. Indeed, they go far beyond that, asserting that, in essence, environment is all. From what I?ve been reading thus far, the second strongest strain of reaction to Jolie?s announcement (after revulsion at the ?mutilation? of women that it represented to certain quacks) is pure denial that mutations in BRCA1 and BRCA2 genes portend such a high risk of ultimately developing breast cancer. This denial is often accompanied by conspiracy mongering about BRCA1 and BRCA2 mutations being a ?conspiracy? on the part of the ?cancer industry? and Myriad Genetics & Laboratories, the company that holds the patents on BRCA1 and BRCA2, to increase genetic testing and preventative mastectomies. Myriad happens to have a complete monopoly on BRCA1 and BRCA2 testing because of this patent and has been criticized for its high prices and stifling of competition. There is currently a case before the U.S. Supreme Court regarding whether human genes are patentable under the law. I?m not a big fan of Myriad, and I?ll tell you why later. (Not that it matters; I?m stuck with them for now.) My personal distaste for Myriad Genetics aside, this sort of conspiracy mongering is part and parcel of the quack approach to denying the significance of BRCA1 mutations.

This denial is usually coupled with confident blather that Angelina Jolie didn?t need to undergo ?disfiguring? surgery to prevent BRCA1-associated breast cancer but instead could have achieved the same?or even better!?risk reduction if only she had used this magic herb or that miracle supplement and making certain ?lifestyle? changes. It?s utter nonsense, of course, but it?s everywhere.

Before I get to the reactions to Jolie?s announcement, let?s first take a look at what she did, why, and the science behind it.

BRCA mutations, Angelina Jolie?s cancer risk, and preventative surgery

On May 14, in the NYT editorial page, after recounting how her mother had battled breast cancer for nearly a decade only to succumb to it at age 56, Angelina Jolie described trying to reassure her children that she wouldn?t die the same way, announcing:

We often speak of ?Mommy?s mommy,? and I find myself trying to explain the illness that took her away from us. They have asked if the same could happen to me. I have always told them not to worry, but the truth is I carry a ?faulty? gene, BRCA1, which sharply increases my risk of developing breast cancer and ovarian cancer.

My doctors estimated that I had an 87 percent risk of breast cancer and a 50 percent risk of ovarian cancer, although the risk is different in the case of each woman.

Only a fraction of breast cancers result from an inherited gene mutation. Those with a defect in BRCA1 have a 65 percent risk of getting it, on average.

Once I knew that this was my reality, I decided to be proactive and to minimize the risk as much I could. I made a decision to have a preventive double mastectomy. I started with the breasts, as my risk of breast cancer is higher than my risk of ovarian cancer, and the surgery is more complex.

BRCA1 and BRCA2 are genes in which certain mutations are most commonly associated with either breast or ovarian cancer, although they are also associated less strongly with several other cancers as well, such as cervical cancer, uterine cancer, pancreatic cancer, early onset prostate cancer (men) and colon cancer (BRCA1) or pancreatic cancer, stomach cancer, gallbladder and bile duct cancer, and melanoma (BRCA2). BRCA1 codes for a protein known as breast cancer type 1 susceptibility protein, a protein belonging to the RING-type zinc finger (RNF) family whose function involves repairing damaged DNA. Specifically, it repairs double-stranded breaks. In the nucleus of a variety of normal cells, the BRCA1 protein interacts with other proteins, such as RAD51 and BARD1, to repair double stranded breaks resulting from radiation and other environmental exposures, as well as breaks that occur during natural processes, such as homologous recombination. The BRCA1 protein is important in multiple functions, including transcription (conversion of the DNA sequence to RNA message), repair of double-stranded DNA breaks, ubiquitination, and other functions. If BRCA1 can?t repair the break, it then promotes cell cycle arrest and apoptosis (programmed cell death). The result of defects in BRCA1 function is increased sensitivity to anything that causes DNA damage and an increased risk of the development of cancer. BRCA2 encodes a protein that, while very different in structure from BRCA1, serves a similar function, namely the repair of double-stranded DNA breaks.

Mutations in BRCA1 and BRCA2 are associated with familial cancer syndromes, most commonly involving breast and ovarian cancer, but not limited to these cancers. Moreover, it needs to be understood that BRCA mutations are not binary. You do not either ?have the mutation? or not. There are many mutations, some of which confer high risk of cancer, others of which confer increased risk but not nearly as high, and some of which whose significance is unknown. In other words, BRCA mutations produce a spectrum of increased risk, ranging from the 87% lifetime risk of breast cancer cited by Angelina Jolie based on the mutation she has to unknown significance (and possibly not even any increased risk of breast cancer). The same is true of BRCA2 mutations, although the maximal risk for breast cancer even the worst mutations in BRCA2 produce are not as high as the maximal risk from BRCA1 mutations. In any case, a good genetic counselor will go through these risks and explain the significance of the dozens of mutations that are known. Either that, or quacks will seize upon various BRCA mutations of either unknown significance or that produce only mildly elevated risk, as though these were the mutations for which doctors recommend preventative surgery. This complexity is why I?m a firm believer that genetic testing for BRCA mutations should usually not be done outside of a center with either skilled genetic counselors or a physician trained in genetic counseling who can explain the risk and help the patient weigh the pros and cons of genetic testing and, if that testing is positive, the various surveillance and preventative strategies available for women carrying BRCA mutations. Also very important is to weigh the ethical and practical issues of genetic testing, such as whether a mutation carrier should inform her family, what effects that it might have on her ability to obtain health insurance, and the many other issues that are inextricably bound with genetic testing, not the least of which is affordability.

In other words, recommendations should be personalized by practitioners using science-based practice. (I know. I couldn?t resist.) It should also be remembered that in the US, BRCA mutations account for only a small minority of cases of early onset breast cancer (2-3%) and ovarian cancer (8%), a proportion that can vary widely based on geography and ethnicity. To put it another way, approximately 25% of women with a breast cancer diagnosis are younger than 50 years, and almost 10% of these women will have a BRCA mutation So, while there is a point to be made that most breast cancers are not associated with BRCA mutations, for carriers of mutations with a high risk of breast or ovarian cancer the mutation is already there, and the risk is already there. The point no longer applies.

All of this leads to recommendations regarding who should be screened. At my cancer center and many others, we use the recommendations of the National Comprehensive Cancer Network (NCCN) guidelines (summarized here). These include:

  • A personal history of breast cancer at age 50 or younger
  • A personal history of triple negative breast cancer (breast cancer that is estrogen receptor-negative, progesterone receptor-negative and HER2/neu receptor-negative)
  • A personal or family history of male breast cancer
  • A personal or family history of bilateral breast cancer (cancer in both breasts)
  • A personal history of ovarian cancer
  • A parent, sibling, child, grandparent, grandchild, uncle, aunt, nephew, niece or first cousin diagnosed with breast cancer at age 45 or younger
  • A mother, sister, daughter, grandmother, granddaughter, aunt, niece or first cousin diagnosed with ovarian cancer
  • A family history of both breast and ovarian cancers on the same side of the family (either mother?s or father?s side of the family)
  • Ashkenazi Jewish heritage and a family history of breast or ovarian cancer

Indeed, there is even a little BRCA mutation carrier risk calculator that can be used to estimate a patient?s risk of being a mutation carrier based on family and personal history.

In the end, although Angelina Jolie tells us that she is a BRCA1 mutation carrier, she does not tell us which specific mutation she carriers. She does tell us that her doctors told her that the specific mutation conferred upon her an 87% lifetime risk of developing breast cancer and a 50% lifetime risk of ovarian cancer. As a result, she decided to undergo a prophylactic bilateral mastectomy with immediate reconstruction and apparently will undergo bilateral oophorectomy (removal of her ovaries) later, her rationale being that her risk of breast cancer is higher and her breast surgery was ?more complex.? It?s not an unreasonable rationale for prioritizing preventative surgery that way.

What Angelina Jolie did

Conceptually, what Angelina Jolie decided to do was simple, but the actual mechanics of carrying it out was complex. Basically, to put it bluntly, she decided to have both of her breasts removed. That?s the big picture, the basic decision. However, there is often a lot more to bilateral mastectomy than just removing the breasts, particularly when one factors in the options for reconstruction. A woman like Angelina Jolie is exceedingly unlikely to have a bilateral mastectomy without some form of immediate reconstruction, given her career. Some women choose this option, however, and their choice must be respected.

Jolie decided to have her breast surgery done through a clinic that I?ve heard of before, the Pink Lotus Breast Center, which advertises itself thusly:

The Pink Lotus Breast Center is a comprehensive and integrative breast center exclusively dedicated to the prevention, screening, diagnosis and treatment of breast cancer.

Expedited scheduling; quick answers; less stress; top doctors; female-run; not hospital-owned; no facility fees; and a single location for all of your needs. Just a few of the many reasons why PLBC?s integrative approach to breast care is unsurpassed and puts each patient first, every single time!

If you think this doesn?t sound promising, you?re correct to a point. Pink Lotus first came to my knowledge when Sheryl Crow had her breast cancer treated there by partial mastectomy (colloquially called ?lumpectomy?). She now has an imaging center Pink Lotus named after her. Apparently, Shannon Tweed was also treated there. Unfortunately, Pink Lotus is not above using these celebrities rather shamelessly to promote itself, as a quick perusal of its website will show, including Sheryl Crow?s Ultimate Breast Cancer Prevention Guide, which is chock full of questionable recommendations and overblown assertions, including recommendations to drink lots of green tea for breast cancer prevention.

The Pink Lotus Breast Center also features a detailed description of the treatment Angelina Jolie underwent written by her surgeon Dr. Kristi Funk, whose credentials appear quite impressive (although I must admit that I couldn?t find any publications on breast cancer by her on PubMed, although it is certainly possible that they were published under her maiden name, which I do not know). Unfortunately, she is also enamored of ?integrative medicine.? Angelina Jolie appears to have undergone a mixture of the science-based (bilateral prophylactic mastectomy for risk reduction due to BRCA1 mutations) tinged with pure pseudoscience, like recommending homeopathic remedies such as Arnica Forte (which consists of Arnica Montana 30x, Bromelain, Antioxidants, Bioflavonoids) as a means of decreasing bruising during surgery, plus Exchem and Lymphomyosot (?to help eliminate anesthesia from the system?). Yes, I?m referring to ?detox,? which is the purpose for which Lymphomysot is advertised.

From a strictly surgical point of view, three aspects of Jolie?s care caught my eye. First, she chose implants for reconstruction rather than tissue flaps. Next, of course, was the ?nipple delay,? in which the tissue underlying the nipple is cut in order to ?improve the blood flow.? At the time this tissue is cut, a biopsy is taken of the ductal tissue underlying the nipple in order to rule out cancer. The idea is that the nipple delay procedure cuts the normal blood supply to the nipple three weeks ahead of time and thus ?forces? the nipple to rely on the surrounding skin for its blood supply, thus making the chance of nipple necrosis (in which the nipple turns black and falls off due to low blood flow) much less likely. It?s a procedure usually reserved only for patients who have had previous breast surgery around the nipple. Not having looked into the scientific literature on the procedure for a long time, I decided to do a bit of searching in PubMed to see if I could find more science-based information about it. In reality, there is little or no evidence that nipple delay is useful as a routine procedure in women of average risk of nipple loss after nipple-sparing mastectomy; its use is generally indicated only in women thought to be at a high risk for nipple loss due to previous surgery in the area, as summarized in this study by noted breast surgeon Armando Giuliano, which concluded that ?surgical delay of the nipple areolar complex 7?21 days before nipple-sparing mastectomy allows safe preservation of the nipple?areolar complex in patients who generally would not be considered candidates for nipple-sparing mastectomy.? Now maybe Angelina Jolie had previous surgery in the area of the nipple-areolar complex. We know she didn?t have ptotic breasts. On the other, Angelina Jolie was a smoker, and there are lots of reports that she still is a smoker. That is definitely a risk factor for wound complications after breast surgery, thanks to decreased blood flow. So maybe that?s the reason why she was offered a nipple delay, although that alone doesn?t seem like enough.

Finally, more questionable is the use of a procedure known as prophylactic dye injection. During breast cancer surgery, we do a procedure known as sentinel lymph node (SLN) biopsy, which involves injecting (usually) two kinds of dye before surgery: A short-lived radiotracer and a blue dye, both of which are taken up by the lymphatics and head to the first draining lymph node (or lymph nodes) under the arm, known as the axillary lymph nodes. These nodes are removed and checked for cancer. In the old days (about 12 to 15 years ago), we used to remove all the lymph nodes under the arm in a procedure known as axillary dissection. These days, we get the same information (whether the axillary lymph nodes are involved or not) with much less morbidity using the sentinel lymph node procedure. When we do prophylactic mastectomies, however, we don?t know if there?s cancer there. There probably isn?t, although there might be. Consequently, we usually do sentinel lymph node biopsies, in case there is cancer in one of the breasts, because once the breast is gone we can no longer do that procedure, and SLN biopsy is pretty low risk. However, that is not acceptable at Pink Lotus, or so it would appear:

Whenever a breast contains cancer and the armpit lymph nodes cannot be felt on exam, we routinely perform a sentinel node biopsy, which is the removal of the first nodes that receive breast lymphatic drainage. By injecting blue dye into the breast, which then travels to the lymph node(s), we find out if cancer spread beyond the breast. Until now, the trend has been not to perform sentinel node biopsies in conjunction with prophylactic (preventive) mastectomies since the discovery of cancer in breasts removed prophylactically only ranges from 2-8%. Therefore, most women do not want to take the additional risks associated with a sentinel node biopsy, especially since they can have complications, such as pain, numbness, arm swelling (lymphedema), fluid buildup (seroma), limited arm movement, and infection. This dilemma has been resolved with a new technique that was pioneered at the Pink Lotus Breast Center, called Prophylactic Breast Dye Injection, or PBDI. PBDI allows the sentinel node to be identified, but not surgically removed, giving more control and peace of mind to women. I developed this technique while treating Angelina, and I hope other women will now benefit from it. It was at her friendly insistence that I wrote the rationale for it in our blog post, Prophylactic Breast Dye Injection.

If you peruse the rationale published by Dr. Funk, you?ll find that she invented this procedure in February 2013. I?ll actually give Dr. Funk credit. PBDI is actually not a bad idea. In fact, in concept, it?s a pretty good idea. However, by Dr. Funk?s own admission, it?s also a new idea thought up by her while treating Jolie that is completely unproven. (One wonders whether Jolie balked at bilateral SLN biopsy.) Hence, from my perspective it is irresponsible to promote PBDI in the context of Angelina Jolie?s surgery given that, also by Dr. Funk?s own admission, there is no evidence for the superiority (or even non-inferiority) of the procedure compared to standard sentinel lymph node biopsy. She even includes a disclaimer:

Disclaimer: We at the Pink Lotus Breast Center have started using the PBDI technique very recently. It is currently unknown which factors influence the precise length of time that the dye remains in the sentinel nodes. Further studies in that regard are needed.

In that case, Dr. Funk and colleagues should be doing preclinical trials in animals and clinical trials in humans to answer the question of what factors determine how long the dye persists in the sentinel nodes and why, not offering this procedure to, in essence, any woman undergoing prophylactic mastectomy.

Still, Angelina Jolie did undergo an appropriate procedure (overall) after finding out that she carried a dangerous BRCA1 mutation, and I can?t criticize her for that. Having done so, according to a recently published model, she has significantly decreased her risk of dying before age 70. For example, a typical 25 year old woman has an 84% chance of living to be 70. Of those not surviving, 11% die of breast or ovarian cancer, the rest of other causes. However, a 25 year old woman with a BRCA1 mutation who undergoes no screening or preventative treatment has only a 53% chance of living to be 70. 77% of the women with BRCA1 mutations who die before 70 die from breast or ovarian cancer. The effectiveness of interventions to reduce risk are summarized below (PO = prophylactic oophorectomy; PM = prophylactic mastectomy):

With no intervention, survival probability by age 70 years is 53% for BRCA1 mutation carriers versus 84% for the general US population (Table 2). The most effective single intervention is PO at age 40, yielding a survival probability of 68% by age 70, which represents a 15% absolute gain compared with no intervention (68% v 53%). Delaying PO to age 50 yields half the survival gain provided by PO at age 40 (8%: 61% v 53% with no intervention). In comparison, PM at age 25 yields a 13% gain relative to no intervention, whereas delaying PM to age 40 yields a small (2%) decrement in gain compared with PM at age 25. Breast screening alone from ages 25 to 69 yields the lowest gain (6%).

The most effective combination strategy is PM at age 25 plus PO at age 40, providing a 26% survival gain by age 70 compared with no intervention (79% v 53%). Postponing PM until age 40, in the presence of screening from ages 25 to 39 and PO at age 40, reduces survival gain by 2%. Eliminating PM and substituting breast screening from ages 25 to 69 while performing PO at age 40 reduces survival gain by an incremental 3%. When added to PO at age 40, breast screening offers 5% lower survival probability than does PM at age 25 (74% v 79%) and 3% lower survival probability than does PM at age 40 (74% v 77%). If PO is delayed until age 50, breast screening offers 5% lower survival probability than PM at age 40 (69% v 74%). Results by age 80 are similar (Table 2). Figure 1A presents survival probability, and Figure 2A presents distribution of health status by age 70 years in BRCA1 mutation carriers under various intervention scenarios.

There is copious other literature that prophylactic surgery can greatly decrease the risk of death due to breast or ovarian cancer in BRCA1 and BRCA2 mutation carriers. Indeed, prophylactic surgery tends to be the single most efficacious intervention for this purpose, although intensive screening with MRI and mammography can also be effective for breast cancer mortality reduction. (Unfortunately, there is no good screening test for ovarian cancer, which tends to be deadlier, making this option much less attractive.) It should be noted, however, that it is not foolproof and does not reduce the risk of cancer to zero. Mastectomies do not remove every last cell of breast epithelial tissue at risk for cancer, for instance. We as practitioners of science-based medicine must be careful not to oversell the benefits of preventative surgery for cancer.

Unfortunately, cranks have no such qualms about exaggerating the harms and minimizing the benefits of such surgery.

Angelina Jolie and science-based medicine versus genetics denialism

It took less than a day for various quacks to attack Angelina Jolie?s decision, as reasonable and science-based as it was, to undergo prophylactic bilateral mastectomies to prevent breast cancer. First out of the box, as is all too frequently the case when it comes to despicably using and abusing celebrity health stories, was the ?Health Ranger? Mike Adams, founder of the NaturalNews.com website. He?s done it before many times, for example about Patrick Swayze?s pancreatic cancer. Then, of course, he worked himself into a fine lather of righteous indignation over Christina Applegate?s ?maiming? when she announced that she had undergone bilateral mastectomies for her breast cancer and a BRCA1 mutation. You can tell a lot by Adam?s chosen title, Angelina Jolie inspires women to maim themselves by celebrating medically perverted double mastectomies.

First, you need to take note. The purpose of this article is blatant, and it?s to sell stuff. After Adams has seemingly gotten his readers all fired up over the horror of Jolie?s decision to ?maim? herself, the very last section of the article advertises this:

Inform yourself and you can protect your body from the insane, knife-wielding cancer surgeons. Get the New Cancer Solutions CD set and empower yourself with real answers rather than cancer industry disinformation and deadly propaganda.

It comes complete with a video (included in Adams? despicable article) that has to be seen to be believed, entitled The female anatomy of Modern Medicine. In any case, the CD includes a talk by Adams himself entitled The Consciousness of Cancer, which is billed as a ?new way? of looking at cancer. No doubt it is, but also no doubt it is a way that has nothing to do with science. From the title, my guess is that Adams subscribes to something similar to the German New Medicine or Andreas Moritz?s ?wisdom of cancer cells? quackery, in which cancer is represented as a survival mechanism.

Now that that point is out of the way (and it?s arguably the most important point, which is why I skipped to the end of Adams? screed first), Let?s get a real taste of what Adams thinks, if you can stand it and if you can call it ?thinking?:

Angelina Jolie announced yesterday that she had both of her breasts surgically removed even though she had no breast cancer. She carries the BRCA1 gene, and she has been tricked into believing that genetic code is some sort of absolute blueprint to disease expression ? which it most certainly is not. Countless millions of women carry the BRCA1 gene and never express breast cancer because they lead healthy, anti-cancer lifestyles based on smart nutrition, exercise, sensible sunlight exposure and avoidance of cancer-causing chemicals.

Jolie, like many other women who have been deluded by cancer quackery, decided the best way to prevent the risk of breast cancer was not to lead a healthy, anti-cancer lifestyle, but rather to surgically remove her breasts in what she describes as ?three months of medical procedures.?

?just in case, you know. Because you can never be too careful these days, with the cancer industry scaring women half to death at every opportunity. ?My breasts might murder me!? seems to be the slogan of many women these days, all of whom are victims of outrageous cancer industry propaganda and fear mongering.

And later Adams adds:

Oh, what a mess Jolie has made of herself. She has maimed her own body with no medical justification whatsoever, then celebrated this horrible disfiguration through some sort of twisted perception of what womanhood really is. Being an empowered woman doesn?t mean cutting off your breasts and aborting live babies ? even though both of these things are often celebrated by delusional women?s groups. Being an empowered woman means protecting your health, your body and your womanhood by honoring and respecting your body, not maiming it.

And, Adams ?coup de grace?:

Wonderful? To cut off parts of your body that have NO disease? With this logic, abortions are cancer prevention, too, because those babies might one day grow up and develop tumors. Better to kill them early and ?prevent cancer,? right?

One can?t help but note that Adams is indulging in a favorite pastime of quacks every where: Denialism of genetics and wishful thinking that genetics doesn?t rule. Yes, it?s true that in some cases genetics doesn?t rule. If a gene doesn?t have a high penetrance, interacts with other genes, or has an activity that is highly influenced by environment, genetics isn?t always destiny, but in the case of the particular BRCA1 mutation that Jolie reports having, there is an 87% lifetime risk of developing breast cancer. Given that breast cancer is a type of cancer that is not highly lifestyle- and diet-dependent (note, that is not to say that lifestyle and diet have no effect, just that the effect tends to be relatively small), no amount of ?anticancer lifestyle, ?smart nutrition,? and ?avoidance of cancer-causing chemicals? is going to lower that 85% chance of breast cancer by very much, no matter how much Adams? wishful thinking might try to mislead other women that such interventions can.

Adams then followed up with a post entitled
How Angelina Jolie was duped by cancer doctors into self mutilation for breast cancer she never had:

With her breasts removed, she says her risk of breast cancer is now reduced to a mere 5 percent. The same bizarre logic can also be applied to men who cut off their testicles to ?prevent testicular cancer? or people who cut out their colons to ?prevent colorectal cancer.? But that would be insane, so nobody does that, because one of the most basic principles of medicine is that you don?t subject patients to the considerable risks and costs of surgery and anesthesia to remove organs that have no disease!

If there existed a gene mutation that conferred a similar risk of testicular cancer as Angelina Jolie?s BRCA1 mutation does for breast cancer, you can be assured that there would be consideration of prophylactic surgery or medication. Also, people do remove their colons to prevent colorectal cancer. Adams is even more ignorant than I thought, apparently never having heard of, for example, familial adenomatous polyposis (FAP). It?s a condition in the colon in which there are numerous polyps that predispose patients with condition to colon cancer such that by age 40 or 50 the risk approaches 100%. The treatment? Prophylactic colectomy. Yes, that?s right, removal of the colon to prevent colorectal cancer. There?s also hereditary non polyposis colorectal cancer (HNPCC), which involves a mutation in a gene with a similar function to that of BRCA1, the gene in which Angelina Jolie had a mutation that predisposed to breast cancer, specifically a gene involved in the repair of DNA damage. The risk from HNPCC isn?t as high as it is for FAP, but it?s plenty high, more than high enough to justify prophylactic surgery to avoid colon cancer.

Sadly, Adams is not alone in his ignorance of oncology. There?s also Sayer Ji, who claimed that vaccines are ?transhumanism? that subverts evolution and made one of the most spectacularly clueless arguments against evidence-based medicine I?ve ever seen, dismissing it as a ?coin flip.? This time around, Ji?s denying that genes cause cancer, the same way that Adams did, but he tries to put a ?science-y? sounding gloss on the statement:

Despite the commonplace refusal of so-called ?evidence-based medicine? to acknowledge the actual evidence of genetics, we moved into a Post-Genomic era over a decade ago following the completion of first draft of the entire human genome in 2000. At that moment, the central dogma of molecular biology ? that our DNA controls protein expression, and therefore disease risk ? was disproved. Our genome was found to contain roughly 20,000 genetic instructions ? not even enough to account for the 100,000 proteins in the human body!

As a result, we must now accept that factors beyond the control of the gene, known as epigenetic factors, and largely determined by a combination of nutrition, psychospiritual states that feed back into our physiology, lifestyle factors, and environmental exposures, constitute as high as 95% of what determines any disease risk. In fact, even the psychological trauma associated with being diagnosed with cancer can drive malignancy via adrenaline-mediated multi-drug resistance,[i] and according to a recent NEJM study, lead up to a 26-fold increased risk of heart-related deaths in the seven days following diagnosis.[ii]

Epigenetics. You keep using that word. I do not think that it means what you think it means. Ji also doesn?t seem to understand that through alternative splicing and various other mechanisms, one gene can easily produce multiple different proteins. Not only is Ji ignorant of oncology, but he?s ignorant of biology.

Ji also beats on the straw man that I mentioned at the very beginning of this post, namely the belief that you either ?have the gene? or don?t when it comes to BRCA1 and BRCA2. Indeed, he even goes so far as to twist himself in knots when he perseverates over an observation that there is actually a known BRCA2 mutation that has been associated with a lower risk of cancer. So what? The existence of such a mutation is irrelevant to the question of whether Angelina Jolie made the right choice in undergoing bilateral mastectomy.

If you don?t believe me when I say that cranks and quacks completely deny the reality that certain gene mutations are so highly associated with cancer, I can?t resist finishing with some truly ignorant commentary by a man named Richard Schulze, a.k.a., the Herb Doc. First, Schulze denies that BRCA1 is even a problem:

But specifically, with breast cancer, scientists think that they have discovered a gene, they refer to as BRCA1, that is a genetic marker for the potential development of breast cancer. The reason I say ?think? is simply because almost all this testing science is proven false or at least faulty a decade or so later, like the AIDS test, or the PSA test for prostate cancer (that has now been proven defective), or giving millions of mammograms to young women whose breast tissue was too dense to see anything, which caused breast cancer and so this practice is now condemned. Regardless of the history of medical testing blunders, many women who test positive for this particular BRCA1 gene are now opting to have their healthy breasts removed, as did Angelina Jolie in February.

And I am telling you right now, that in a decade or two, surgically cutting off healthy breasts because someone tests positive for the BRCA1 gene will be seen as a huge horrific medical mistake.

Maybe so, but only if sometime between now and two decades from now we discover a drug that reduces the risk of breast cancer in BRCA mutation carriers as much as prophylactic surgery does. Even in that case, depending on the safety and efficacy of the drug, it wouldn?t be an unreasonable decision to opt for a one-time surgery over potentially decades of taking a pill every day. Besides, we have to work within the context of the science that we have now. For example, the Halsted radical mastectomy, as ?barbaric? as it is perceived now, was not an unscientific or inappropriate treatment 100 years ago. Given that adjuvant chemotherapy and radiation therapy did not exist back then, if a cancer was going to be cured, surgery was the only modality that could cure it. Given that there was no mammographic screening back then, most breast cancers were pretty large by the time they were noticed; so if surgery was the only way to cure breast cancer, then it had to be radical surgery to get all of it. And the radical mastectomy was more efficacious than any other procedure at the time. Surgery?s mistake was to continue to do more radical surgery once evidence beginning in the middle part of the last century started to make it clear that such radical surgery was not necessary. But that?s a minor issue compared to Schulze?s mix of misinformation (HIV denialism, misunderstanding of mammography, and the like) with issues that medical science, not quacks, is already working on correcting. None of this stops Schulze from opining:

All that genetic markers say is that you have the potential to develop a disease, like breast cancer. It simply means that you have genes in your body, that when stimulated, irritated or woken up, can mutate and develop into cancer. Well, what wakes these genes up is no mystery, and ALL medical and cancer researchers know exactly what turns these genes on, but they don?t want to touch this subject, simply because it?s unpopular. What turns these genes on and makes them mutate, is junk food, toxic chemicals, French fries, pharmaceutical drugs? the list is long; it?s the aftermath of the American Dream.

Except that, in the presence of genetic markers as strongly associated with cancer as BRCA1 and BRCA2, there is very little that diet, lifestyle, and the like can do to lower the risk significantly. There is one thing, though, at least in the case of BRCA2-related breast cancers, that is quite effective in lowering risk, but Schulze won?t like it. I?m talking about Tamoxifen, which significantly reduces the risk by as much as 62%. Unfortunately, it?s not as clear whether Tamoxifen is as effective in preventing BRCA1-associated tumors because they tend to be estrogen receptor-negative. Either way, contrary to what Schulze is saying, it?s not diet and lifestyle that can reduce risk in the case of BRCA mutations. It?s either surgery or?gasp!?pharmaceutical drugs.

The bottom line

Celebrity health stories like that of Angelina Jolie are a two-edged sword. On the one hand, Jolie made a perfectly rational, evidence-based choice to undergo prophylactic bilateral mastectomy. I don?t like the center she chose or how that center uses ?integrative medicine? and seems a bit too eager to jump the gun on using surgical procedures that haven?t yet been validated in clinical trials, but her overall decision, if you can ignore the mechanics of how she carried out that decision, was sound. As such, her story can raise awareness and potentially help increase the rate of genetic testing in women who are candidates for it, as genetic counseling and testing are woefully underutilized.

Her case also publicizes various socioeconomic and political issues. There?s no doubt about it, Jolie is filthy rich, thanks to the success of her and her fiance Brad Pitt in Hollywood. She has access to the best of everything, and she doesn?t have to worry about paying for BRCA testing, prophylactic mastectomy, or the very finest breast reconstructive surgery available. Most women can?t say that, and, unfortunately, as has been pointed out, the issue of genetic testing can result in dilemmas for some women. Although the Patient Protection and Affordable Care Act will, when fully implemented, require that appropriate, evidence-based genetic testing and preventative surgery be covered, until now many women could not afford genetic testing and did not have insurance companies that covered preventative surgery, much less breast reconstruction. Moreover, there is the potential problem that publicity will result in a push for more screening in women for whom there is not an indication, with the potential to cause harm.

Finally, there is the issue of the gene test itself, on which Myriad Genetics has a monopoly. If there?s one thing the quacks have written that has a bit of traction, it?s the criticism of Myriad, whose patent has crushed any competing BRCA mutation tests. I said before I?m not a fan of Myriad. I view its stranglehold on BRCA testing as stifling innovation, which is why I?m glad that the U.S. Supreme Court is hearing a case against Myriad about the legal validity of its patents. Even though Myriad?s patents are only good for two more years, one can only hope that a precedent is established. I also can?t help but wonder whether all these newer next generation sequencing tests coming out will mean the end of Myriad?s monopoly anyway, given that they will give information on all potential cancer-associated gene mutations, including BRCA mutations. To the extent that the Angelina Jolie case sheds light on this issue, it?s all to the good.

In the end, leaving aside all these political and class issues, however, the decision regarding preventative surgery is an intensely personal one. Angelina Jolie made her decision based on evidence, and I can?t argue with her decision. Were she my patient, I would have counseled her to do what she did, minus the homeopathic remedies ?integrated? into her care. What I find particularly ironic is how a common theme running through so much of the criticism quacks are sending Jolie?s way is that she made the wrong decision, that she was ?duped? by the ?cancer industry.? The contempt, although denied with a disclaimer of how they ?understand? how difficult the decision was, is palpable. I thought ?alternative? health was all about empowering the patient to make her own decisions. Apparently such ?empowerment? is only admirable to people like Mike Adams, Sayer Ji, and Robert Schulze, if the empowered patient makes a decision they agree with.

Source: http://www.sciencebasedmedicine.org/index.php/angelina-jolie-radical-strategies-for-cancer-prevention-and-genetics-denialism/

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