4.8 Article

Transformation of the Fallopian Tube Secretory Epithelium Leads to High-Grade Serous Ovarian Cancer in Brca;Tp53;Pten Models

期刊

CANCER CELL
卷 24, 期 6, 页码 751-765

出版社

CELL PRESS
DOI: 10.1016/j.ccr.2013.10.013

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资金

  1. National Institutes of Health
  2. SPORE [P50 CA105009]
  3. EDRN [U01 CA152990, R21 CA156021]
  4. DOD OCRP [W81XWH-10-1-0263]
  5. American Cancer Society [RSG-13-083-01-TBG]
  6. Ovarian Cycle and Ovarian Cancer Research Fund Liz Tilberis award
  7. Burroughs-Wellcome Fund Career Award in the Biomedical Sciences [1005320.01]
  8. V Foundation for Cancer Research Scholar Award
  9. Marsha Rivkin Foundation for Ovarian Cancer Research
  10. Mildred Moorman Ovarian Cancer Research Fund
  11. Dr. Miriam and Sheldon G. Adelson Medical Research Foundation
  12. Ovarian Cancer Research Fund Ann Schreiber award
  13. National Ovarian Cancer Coalition
  14. Mary Kay Foundation
  15. Sandy Rollman Ovarian Cancer Foundation
  16. Susan Smith Center for Women's Cancers at the Dana-Farber Cancer Institute
  17. Debra and Robert First Fund
  18. Gamel Family Fund
  19. Eleanor and Miles Shore 50th Anniversary Fellowship Program for Scholars in Medicine Award

向作者/读者索取更多资源

High-grade serous ovarian carcinoma presents significant clinical and therapeutic challenges. Although the traditional model of carcinogenesis has focused on the ovary as a tumor initiation site, recent studies suggest that there may be additional sites of origin outside the ovary, namely the secretory cells of the fallopian tube. Our study demonstrates that high-grade serous tumors can originate in fallopian tubal secretory epithelial cells and also establishes serous tubal intraepithelial carcinoma as the precursor lesion to high-grade serous ovarian and peritoneal carcinomas in animal models targeting the Brca, Tp53, and Pten genes. These findings offer an avenue to address clinically important questions that are critical for cancer prevention and early detection in women carrying BRCA1 and BRCA2 mutations.

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