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Breast Cancer Complexity in Personalized Medicine

Scientists at Washington University School of Medicine in St. Louis have conducted the single largest cancer genomics investigation to date by sequencing the entire genomes of tumor from 50 breast cancer patients.  They compared the cancer DNA to healthy cells in the same patient and found mutations that only occurred in the cancer cells.  They uncovered incredible complexity in the cancer genomes of these tumors that had more than 1,700 mutations, most of which were unique to the individual.

To undertake this study, the Oncologists and Pathologists worked with the University's Genome Institute to sequence more than 10 trillion chemical bases of DNA - repeating the sequencing of each patient's tumor and healthy DNA about 30 times to ensure accurate data.  Huge computing facilities were required to analyze this amount of data.  All patients in the trial had estrogen receptor positive breast cancer.

The researchers found that two mutations were relatively common in many of the patient's cancers. Once is present in about 40% of estrogen positive breast cancer and the other present in about 20%.  They found a third mutation that controls programmed cell death and is disabled in about 10% of estrogen-receptor-positive cancers.  This mutated gene allows cells that should die to continue living.  Only two other genes had mutations that recurred at the 10% level.

They found 21 genes that also significantly mutated, but at much lower rates.  Even though these mutations were relatively rare, they still involve thousands of women and are very important to understand.

These highly detailed genome maps are an important first step to designing therapy that is personalized to the patient.  We do not know why treatment works for some women and not others.  It may also help us understand aggressive types of breast cancer that are difficult to treat and occur in young women and African-American women.

Individual and personalized medicine is only possible when the cancer's genetics are known in advance.  We are getting closer each day.


jobb said…
Do adverse mutations occur as a result of any known cause? Are there any known inhibitors to these mutations? It does sound as if these discoveries are on the right track.
thanks for your post .I agree with your point.
Best Skin Care said…
Im glad their getting more clear view of how they cure and make treatments for breast cancer, in time they'll make medication work out well.

Jake Smith
Jonathan said…
This is really exciting stuff, and a move towards Dx before Rx, and an Rx that could ultimately be tailored to the individual as you've pointed out.
To my mind every person ought to browse on it.

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