articleProceedings of the National Academy of SciencesOct 17, 2011BRONZE OA

Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing

Medical Genetics Center · Gynecologic Oncology Group · +1 more institution

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Abstract

Inherited loss-of-function mutations in BRCA1 and BRCA2 and other tumor suppressor genes predispose to ovarian carcinomas, but the overall burden of disease due to inherited mutations is not known. Using targeted capture and massively parallel genomic sequencing, we screened for germ-line mutations in 21 tumor suppressor genes in genomic DNA from women with primary ovarian, peritoneal, or fallopian tube carcinoma. Subjects were consecutively enrolled at diagnosis and not selected for age or family history. All classes of mutations, including point mutations and large genomic deletions and insertions, were detected. Of 360 subjects, 24% carried germ-line loss-of-function mutations: 18% in BRCA1 or BRCA2 and 6%…

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Authors

15

Topics & keywords

Keywords
  • Massive parallel sequencing
  • Ovarian carcinoma
  • Biology
  • Ovarian cancer
  • Genetics
  • Cancer research
  • Genetic testing
  • Gene
UN Sustainable Development Goals
  • Good health and well-being
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