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Genetic mutations in tumours help ovarian cancer survival

13 October, 2011

Women with high-grade ovarian cancer live longer and respond better to platinum-based chemotherapy when their tumours have BRCA2 genetic mutations, says a report from researchers at The University of Texas MD Anderson Cancer Center and the Institute for Systems Biology.

 This report was published in the Oct. 12 issue of the Journal of the American Medical Association.

"BRCA2-mutated tumours are more vulnerable to these DNA-damaging agents, which is really exciting because there are a number of drugs in clinical trials now that block DNA repair that might prove effective against these tumours in combinations," said senior author Wei Zhang, Ph.D., professor in MD Anderson's Department of Pathology.

BRCA2 and its cousin, BRCA1, are tumour-suppressing genes involved in DNA repair that, when mutated, raise a woman's risk for having breast or ovarian cancer.

"Uncovering the separate potential effects of BRCA1 and BRCA2 mutations takes us a step towards a more personalized approach to treating ovarian cancer, and perhaps other cancers," Zhang said. "This paper suggests those two genes, and the many others involved in DNA repair, are prime targets for further research."

Past studies of the possible clinical impact of BRCA1 and BRCA2 mutations tended to look at the two genes together and were limited by small sample sizes.

First author Da Yang, Ph.D., an Odyssey Fellow in MD Anderson's Department of Pathology, said their in-depth study was made possible by The Cancer Genome Atlas project. TCGA published a study of 489 cases of  high-grade serous ovarian cancer, the most common form of the disease,  that combined an exhaustive analysis of each tumour's genome with comprehensive clinical data on each patient.

"TCGA gave us enough analytical power to differentiate between BRCA1 and BRCA2 mutations and conduct a survival analysis," Yang said.

Improved overall survival

Of 316 cases, 29 tumours had BRCA2 mutations tumours and 37 had BRCA1 mutations. tumours were similar in grade and stage. 

Findings include:

  •  61 percent of patients with BRCA2 mutations survived for five years, compared with 25 percent of those with normal BRCA2 in their tumours.
  • percent of those with BRCA2 mutations lived three years after surgery and platinum treatment without disease progression, compared with 16 percent of those with normal BRCA2.
  • BRCA1 mutations in tumours were not associated with survival.
  • All of those with BRCA2 mutations responded to platinum chemotherapy, compared to 82 percent with the normal gene and 80 percent whose tumours had BRCA1 mutations.
  • Their response to chemotherapy lasted 18 months, compared with 11.7 months for normal BRCA2 and 12.5 months for BRCA1 mutations.
  • tumours with BRCA2 variations also are hypermutants - they had more genetic mutations - with 84 mutations per tumour sample compared to 52 for normal BRCA2.

Zhang said this last aspect - called the hypermutator phenotype - might be both a factor in the development and growth of the tumour and a sign of its vulnerability.

BRCA2 is normally involved in the repair of double-strand DNA breaks. Cells with BRCA2 mutants are less capable of repair, allowing other genetic mutations to survive and grow, the type of genomic instability that cancer thrives upon.

However, cancer cells in turn rely on DNA repair to defend themselves against DNA-damaging drugs, such as platinum-based agents. So adding drugs that inhibit DNA repair could increase the effectiveness of chemotherapy, Zhang noted. PARP-inhibitors, a new class of drug in clinical trials, block DNA repair and may also be effective in treating BRCA2 mutated ovarian cancer.

Additional studies of the function of BRCA1 and BRCA2 mutations are needed to more fully understand and exploit their findings to treat cancer, Zhang and colleagues note.

The Cancer Genome Atlas is a joint project of the National Cancer Institute and the National Human Genome Research Institute, both of the National Institutes of Health, to comprehensively characterize changes in genetic mutation and regulation of various cancers. 

Source: The University of Texas MD Anderson Cancer Center

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