Why Angelina Jolie Should Leave Her Ovaries Alone

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Why Angelina Jolie Should Leave Her Ovaries Alone

Angelina Jolie has already had her breasts removed, now she is poised to remove her ovaries. What is the rationale and justification? Is it myth or 'hard science" that is driving her towards this radically invasive decision?

With Angelina Jolie's recent announcement that she will be having her ovaries removed due to an inherited BRCA 'defect' and a history of breast and ovarian cancer in her family, once again the pseudo-scientific but still thriving meme that genes play a dominant role in determining biological destiny is proliferating in the mainstream media like the fear-driven mental virus it is.

Last year, in a New York Times Op-Ed titled, "My Medical Choice," Angelina Jolie described why she chose to have a double mastectomy due to a "faulty" gene, BRCA1, and recounted what her doctors told her was the extreme health risk associated with this 'mutation':

"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." 

At first glance, these estimates are frightening. Who, given such a prognosis, wouldn't feel compelled towards aggressive intervention when being told that doing nothing (watchful waiting) results in a statistically verified certainty of a 50% increased risk of contracting the most lethal gynecological cancer in existence. [1]

But where do these numbers come from? How do her misfortune-telling caretakers arrive with any certainty at this figure?

The reality is that the average woman's lifetime risk of ovarian cancer is exceedingly small, with the overall risk of developing ovarian cancer by 65 years of age being 0.8 percent and the lifetime risk 1.8 percent.[2] For those with a first-degree relative developing ovarian cancer, as is the case for Jolie, the risk estimates show increases to 4.4 and 9.4 percent, respectively.[3]  This is the concept of relative risk which can be used as a statistical sleight of hand to amplify perceived danger.

It is also important to realize that lifetime ovarian cancer risk does not exist in a vacuum. It is not cancer (at any site) but heart disease that is the #1 killer of women. In other words, if Jolie simply let her life go on, without radical surgical intervention, it is statistically more likely she would die from heart-related death than cancer of any kind....

The lifetime risk of heart disease related death in women is in top position, according to CDC statistics, at 23.5%, versus cancer which takes #2 position at 22.1%. And within cancer related deaths in women, breast, lung, colorectal cancer, uterine, thyroid, non-Hodgkin's lymphoma and melanomas are top on the list, with ovarian cancer in the 8th in position.

Cancer Stats for Women

Given this context – and we must remember that a text without a context is a pretext -- how Angelina's doctors think it is appropriate to express the relative risk of 50% in a way that colloquially comes off as absolute risk, is a mystery. But even if her prognosticators are accurate at reading the 'tea leaves' of her genome and family history, their attempts at predicting the future reflect a profound misunderstanding of the ovarian cancer statistics as a whole, and the nature of the disease itself.

Ovarian Cancer: Misunderstood and An Epidemic of Overdiagnosis

First, ovarian cancer is highly overdiagnosed, i.e. a labeling of "disease" that will never cause symptoms or death during a patient's lifetime.  In other words, ovarian 'cancer' is being diagnosed in women who do not have it!

According to a JAMA retrospective study of ovarian cancer screening, five times more women without ovarian cancer end up having surgery than those with ovarian cancer.[4]

Yes, these are women who were told they had cancer, but who did not, in fact, have cancer at all, and who ended up having their ovaries removed – including subjecting themselves to other extremely toxic 'treatments' such as radiation and chemotherapy- because they put unfailing trust in their doctors and a medical system that claims to know far more about their bodies – through screening – than they do.

Not only does this overdiagnosis/overtreatment statistic represent an egregious assault upon women's physical and psychospiritual health, with unimaginable suffering as a consequence, but these false-positives inflate the ovarian cancer statistics, making it all the more likely to overestimate the prevalence and risk of ovarian cancer to the average woman in general.

One of the fundamental reasons for ovarian cancer overdiagnosis is that the natural history of ovarian cancer, and age-associated non-cancerous ovarian changes that may be mistakenly interpreted as life-threatening cancers, has not yet been worked out. We are too busy cutting, burning and poisoning these 'abnormalities' to know what they are.

In the same way that so-called early stage breast cancers like ductal carcinoma in situ (DCIS), which for 30 years were treated as life-threatening and malignant -- leading to 1.3 million US women having their breasts unnecessarily removed and their bodies treated with radiation and chemotherapy – were mistakenly classified as 'cancer,' non-malignant abnormalities of the ovaries that develop as women age are only now being understood as also benign and therefore better left untreated. 

"Borderline ovarian tumors comprise about 15%–20% of all epithelial ovarian malignancies [2, 3] with an incidence of 1.8–4.8 per 100,000 women per year [35].

BOTs differ significantly from ovarian carcinomas with regard to percentile distribution of tumor histotypes, lower FIGO stage, excellent overall prognosis, younger age distribution, higher infertility rate, and a lower frequency of BRCA mutations." [Note: while borderline tumors are related to a lower frequency of BRCA mutations, they nonetheless, inflate the statistics so that anyone, BRCA mutation or not, is subject to greater pressure to opt for ovarian removal]

Evidence for the non-malignancy of borderline ovarian tumors (BOTs) is reflected in the 5-year survival rate post-treatment, which is 95%–97% [12]. This is on the same order magnitude as DCIS, which is as high as a 10-year survival rate of 96%-98%. Why so high a survival rate? Because the women diagnosed with the condition and subsequently treated are not surviving 'cancer,' rather, unnecessary surgery, treatment and the psychological traumas that follow the process."

The reality is that modern medicine just doesn't know what BOTs are:

"Borderline ovarian tumors represent a wide spectrum of tumors with different biological potential and uncertain malignant potential. No precise prognostic or predictive markers exist to clearly distinguish between tumors of purely benign behavior and those with risk of malignant transformation into carcinomas. Therefore, the oncologic safety must be always balanced again less radical treatment."

The primary justification today for preemptive ovary and fallopian tube removal -- salpingo-oophorectomy -- is the notion that hereditary determines risk. Family history, for instance, is considered the primary factor in determining whether a woman will end up with ovarian cancer. In other words, if your mother had ovarian cancer, it is believed you will be far more likely to end up with it as well.

The BRCA genes – BRCA1 and BRCA2 -- have been identified as the primary 'cause' for this familial association, in an unsophisticated nod to genetic determinism that has been the prevailing theory for over half a decade. But the reality is that if your mother had been diagnosed with ovarian cancer (perhaps falsely), you are much more likely to seek out medical surveillance for the condition, and are therefore much more susceptible to overdiagnosis and overtreatment yourself, repeating the vicious cycle of iatrogenesis. This is generally not considered when family history related ovarian cancer risk is calculated. And this has everything to do with the medical establishment not coming clean as to its increasingly obvious mistakes.

But there is also a far more insidious aspect to the hereditary-based theory of ovarian cancer risk that is not on the radar of most oncologists, and is certainly not something the mainstream media has reported on. The reality is that BRCA mutation status is not nearly as important as epigenetic exposures – chemicals, nutrient deficiencies and incompatibilies and even emotions – which can 'knock out' the cancer-protective function of the BRCA genes, regardless of whether one was born with 'defective' or 'heathy' version of the gene from the start.

There is also the troublesome data on BRCA1 gene mutation resulting in increased survival from ovarian cancer. As strange as it may seem, the much lauded 'cancer causing' genes have been found in a number of studies to improve outcomes. Here is a sampling of the data:

"BRCA1 heterozygotes developed EOC [epithelial ovarian cancer] at a younger age compared with BRCA2 heterozygotes and women who had sporadic ovarian carcinoma. BRCA heterozygotes had a better response to platinum chemotherapy compared with women who had sporadic disease, which may have contributed to their improved prognosis."

"Although BRCA-associated hereditary ovarian cancers in this population have surgical and pathological characteristics similar to those of sporadic cancers, advanced-stage hereditary cancer patients survive longer than nonhereditary cancer patients. Age penetrance is greater for BRCA1-linked than for BRCA2-linked cancers in this population.

"Compared with controls, BRCA-positive patients had higher overall (95.5% v 59.1%; P = .002) and complete response rates (81.8% v 43.2%; P = .004) to first line treatment, higher responses to second and third line platinum-based chemotherapy (second line, 91.7% v 40.9% [P = .004]; third line, 100% v 14.3% [P = .005]) and longer TFIs. [treatment-free interval]."

This research is actually consistent with BRCA-related breast cancer, insofar as certain 'mutations' actually confer higher breast cancer survival outcomes than would be expected if, indeed, BRCA 'caused' breast cancer. [See 'The Case Against BRCA1 and 2 Testing' Send an email to info@greenmedinfo to receive the full study!]

BRCA Gene Malfunction: Inheritance Is Not As Important as Exposure

A game-changing recent study published in the journal Tumor Biology titled, "BRCA1 promoter hypermethylation and protein expression in ovarian carcinoma – an Indian study," casts serious doubts upon the primary role that the much touted BRCA mutation status has in determining both ovarian cancer risk and treatment outcomes.  BRCA stands for Breast Cancer Susceptibility Gene, and is responsible for producing a protein – BRCA – that suppresses tumors, both of the breast and ovaries. The new study found that epigenetic silencing of the BRCA1 promoter gene – through a process known as gene hypermethylation -- is a common phenomenon in ovarian cancers, affecting about 1 in every 2 ovarian cancers studied. 

Up until now, most of the focus on breast and ovarian cancer risk has been on the inherited BRCA1 mutations and how they interfere with proper BRCA function. The new study reveals that epigenetic processes, working from the outside in, as it were, can produce the same functional outcome as an inherited mutation. BRCA gene deactivation through hypermethylation can be stimulated through chemical exposures, such as to dioxins, for instance. There is also research indicating this can be prevented through natural compounds such as resveratrol and soy, putting diet – and so-called nutrigenomic interventions – at the forefront of cancer prevention and treatment.

We explored the role of 'phytocompounds' in protecting against BRCA silencing (hypermethylation) with nutritional compounds in-depth in a previous article titled, "Beyond the 'Breast Cancer" Gene (BRCA): Why Food Is Your Medicine," wherein resveratrol is identified to suppress the persistent environmental pollutant 2,3,7,8 tetrachlorodibenzo-p-dioxin (TCDD) induced silencing of BRCA.

The fact remains that everyone, man and woman, has the BRCA1 and 2 gene. And everyone faces the risk of chemical exposure with tens of thousands of carcinogens that now exist freely in our environment, food, and body care products. The aforementioned study speaks to how important our choices, our exposures, our diet, affect our cancer risk, and more specifically our gene expression, and whether the patterns of expression will promote health or interfere with it.

The concept – the meme – that hereditary determines one's biological destiny is archaic. After the first draft of the human genome project was completed in 2005, they only found 23,000 genes! That's not enough protein-coding genes to explain the existence of our body, which contains at least 100,000 different proteins. What this epic failure revealed is that it is not the genes themselves that determine health or disease, rather, what factors in our environment, lifestyle and nutrition that activate the expression of certain genes, and silence the expression of others. In the case of BRCA1 and BRCA2, we now know that silencing these genes from the 'outside in' results in the same result as being born with a defective gene from the 'inside out,' with the important difference that epigenetic – 'outside in' – gene silencing can actually be reversed or mitigated. Our genome results from millions of years of evolution, whereas our epigenome is influenced by day to day decisions, many of which depend on what we decide to eat or avoid eating, right now. Choice, therefore, becomes central to determining disease risk. And given that Jolie's decision to remove her breasts, and subsequently her ovaries, was predicated on a belief that she is helpless in the face of predetermined risk – her decision does not reflect the evidence and biological science itself.

How do we end up living in a world where people believe that their genes – which they do not have access to without biomedical surveillance -- determine their destiny?  How we end up thinking that 'gene defects' are so powerful that removing healthy organs from our body is the only reasonable way to prevent experiencing cancer within them?

Let's say you have an increased risk of brain cancer, why shouldn't you remove your head? That way there is absolutely no chance in hell you can contract brain cancer.

The same twisted logic applies to ovarian and breast cancer. Remove your ovaries and breasts, and what chance do you have of contracting cancer within them in the future?

That's the illogical logic operative here.  We must recognize cancer, not as a time-bomb programmed to go off, but as the expression of a hostile environment in the body that cells are attempting to adapt. This is a meme of empowerment, of true prevention, and one that delivers the imperative to clean up our planet, our bodies, and our minds.


[1] National Cancer Institute, Snapshot of Ovarian Cancer: Incidence and Mortality

[2] American Family Physician, Estimating the Risk of Ovarian Cancer, Sept. 2009

[3] Hartge P, Whittemore AS, Itnyre J, McGowan L, Cramer D. Rates and risks of ovarian cancer in subgroups of white women in the United States. The Collaborative Ovarian Cancer Group. Obstet Gynecol. 1994 Nov;84(5):760-4. PubMed PMID: 7936508.

Cited in PMCRelated citations

[4] Clinical Epidemiology: The Essentials  by Robert H. Fletcher, Suzanne W. Fletcher, and Grant S. Fletcher 5th edition published by Wolters Kluwer

Disclaimer: This article is not intended to provide medical advice, diagnosis or treatment. Views expressed here do not necessarily reflect those of GreenMedInfo or its staff.
Sayer Ji
Founder of GreenMedInfo.com

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