The islands of the  Bahamas are known for their beautiful beaches and pristine clear waters, a marvel many across the globe seek out in their travels. Aside from the beautiful waters, and gorgeous beaches there is a third resource that is beyond value, the people. With a rich history, dating back to the discovery of the new world by Christopher Columbus, his very first stop was an island on the eastern side of the chain of Bahamas islands, San Salvador. Following suit, the Bahamas like the rest of the Caribbean became the epicenter of a global economical transition, fueled by an undiscovered continent and the promise of untold wealth. This cultural explosion was fueled on the backs of African slaves immigrated to the New World as a cornerstone to the global expansion of the European settlers. And to this day that great migration is evident in the genetic makeup of the Bahamian people and serves as the basis for the reason why women in the Bahamas have the greatest worldwide risk of hereditary breast cancer.

The BRCA1 & BRCA2 (breast cancer 1/2, early onset) genes were first discovered in 1990, and have since been linked to a genetic predisposition to breast & ovarian cancer in women. Several other studies have linked BRCA genetic mutations to other types of cancer including pancreas and prostate. Research studies have drawn a significant correlation between individuals with a BRCA mutation and incidence of breast/ovarian cancer, with a  greater than >75% lifetime risk. Signifying that women with a BRCA1/2 mutation are very likely to develop either breast or ovarian cancer within the course of their life-time.

This genetic mutation is one of the greatest predictors on cancer among the human race. The good news is that the frequency of BRCA1 mutations is <1% (1 in 500 women) in the general population. However, specific ethnic groups have been shown to have a higher association of BRCA1 mutations, specifically the Ashkenazi Jewish population. This term refers to Jewish people of eastern European descent. In the late 1990s studies have estimated that the overall frequency of BRCA1/2 mutation within the Ashkenazi Jewish population at approx. 2.65% (1 in 40 women). Of Ashkenazi Jewish women who develop breast/ovarian cancer, ~11% were estimated to arise as a result of mutations within the BRCA1/2 gene.

These findings about the association of Ashkenazi Jews and breast cancer risk have initiated a flurry of studies about population-based risk for breast/ovarian cancer via BRCA1/2. As a result the genetics of the Ashkenazi Jewish population have been extensively studied in an attempt to understand how BRCA1 hereditary breast cancer arises. The most frequent mutation of the Ashkenazi Jewish population is 185delAG. This mutation result in an alteration of the gene expression impairing its functions and resulting in the induction of cancer. Until recently this population of women have embodied the association of BRCA1/2 hereditary breast cancer risk, and thus the medical community has invested heavily in understanding the significance of their risk.

However, in 2011 it was discovered that women in the Bahamas have a much higher association of breast cancer risk than even the Ashkenazi Jewish population. Qualitative observation of Bahamian women developing breast cancer at very young ages <40 yrs old, lead to an initial study investigating the frequency of BRCA1/2 mutations in Bahamian women who had developed breast or ovarian cancer. This lead to a conclusion that the women who had developed cancer 23% were due to BRCA1/2 mutations. As whole population studies are currently underway (Bahamas Breast Cancer Initiative Foundation), the overall frequency of BRCA1 mutation within the general population in the Bahamas is yet to be determined. However, estimates suggest that the frequency of this mutation may be as high as 4% (1 in 25 women) within the general Bahamian population. Several types of BRCA1 mutations were observed in the Bahamian population but greater that 90% of the associated BRCA hereditary breast cancer was one specific mutation (IVS13+1G>A) an African founder mutation. The Bahamas is a population with greater than 90% of African descent, therefore a founder mutation previously associated with individuals of African descent is not surprising  and reflects the essence of the African heritage reflected in the DNA of Bahamian people. Even more interesting is that this mutation has not been associated with Ashkenazi Jewish women, indicating a totally different inherent risk association.

So what does this mean? Will there be a rush to study Bahamian women, or even women in the Caribbean of African descent to determine the impact of these mutations on the general population?

In short, where exactly the future of BRCA1 hereditary breast cancer research in the Bahamas will lead no one knows. Initial studies are currently underway and hopefully will yield some answers. However, the Bahamas is not an island with vast medical resources for research and the world seems content with what they think they know about the associated risk of breast cancer via BRCA1. It is clear that these observations need to be studied further. Although we know that BRCA1 mutations indicate a higher risk, there is still a whole lot we do not know. Specifically, what can trigger the onset of breast cancer in individuals with this inherited risk? Additionally, although we know that individuals with known BRCA1 founder mutations will likely develop breast cancer we have yet to determine how to prevent the onset of this disease in those individuals aside from a mastectomy (removal of the breasts) or oophorectomy (removal or the ovaries).

On the reverse side, there are hundreds of types of BRCA1 mutations, and several of these mutations have not been linked to any cancer, and yield no answers on the appropriate approach in individuals with these inconclusive mutations. Therefore we are quite a ways from answering all the questions.

We have reached an age of mass information via our technological resources. We have gained the ability to better unlock the potential of our genes, and read our genetic code like a manual to our future. However, we are still inept at implementing the appropriate solutions when we find a problem.

Research is key to tapping into the code in our DNA, for the right prescription to our ailments. And although BRCA is seen as the holy grail for understanding breast/ovarian cancer risk there are several other known genes that poses association with cancer but are ignored due to the low mutation frequency. What do we do about those?

The solution may not be simple but it begins with a complete understanding of who were are as a people, genetically speaking & what can genetic testing tell us about our risk.







Reference:-

1. Donenberg T, Lunn J, Curling D, Turnquest T, Krill-Jackson E, Royer R, Narod SA, Hurley J., "A high prevalence of BRCA1 mutations among breast cancer patients from the Bahamas."Breast Cancer Res Treat. 2011 Jan;125(2):591-6
2. Akbari M, Donenberg T, Lunn J, Curling D, Turnquest T, Krill-Jackson E, Zhang S, Narod S, Hurley J."The spectrum of BRCA1 and BRCA2 mutations in breast cancer patients in the Bahamas." Clin Genet. 2013 Mar 4.

Photo credit: bookgrl / Foter.com / CC BY-NC-ND

We all have that person who seems like they are always sick. Science has recently discovered that it may be more than just a bum immune system but may boil down to the building blocks of life, DNA via telomere length. For everyone who slept though high school biology, Telomeres are an essential aspect of human biology. But before we say why, lets get down to what a telomere actually is.

A chromosome that is capped by the telomere