Previous research has established a link between genetic mutations in the BRCA1 and BRCA2 genes to an increased risk of developing ovarian, fallopian tube or peritoneal cancer in women. A recent publication documents the efforts of a team of researchers affiliated with the Gynecologic Oncology Group (GOG) to determine if inherited genetic mutations other than BRCA1 and BRCA2 can also put a woman at risk of developing these diseases.
Paul DiSilvestro, MD, head of research with the Program in Women’s Oncology at Women & Infants Hospital and professor of obstetrics and gynecology at The Warren Alpert Medical School of Brown University – published their findings in the article “Inherited Mutations in Women with Ovarian Carcinoma” in the recent issue of the Journal of the American Medical Society.
“Descriptions of the identity of these genes and their frequency was lacking in the medical literature,” Dr. DiSilvestro explains. “The goal of this research was to better define these issues.”
“The results of this trial expanded our knowledge of the genes that we suspect cause hereditary ovarian cancer, bringing the total to 11,” Dr. DiSilvestro says, adding that, “Genetic testing should now begin screening for these nine additional genetic mutations so women carrying the genes can make educated decisions about their health care future.”
Women interested in Cancer Genetics and Prevention Program at Women & Infants. For more information, call (401) 453-7540.
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