High-grade serous carcinoma (HGSC) is the most common and aggressive histotype of epithelial ovarian cancer (EOC), and it is the predominant histotype associated with hereditary breast and ovarian cancer syndrome (HBOC). Mutations in BRCA1 and BRCA2 are responsible for most of the known causes of HBOC, while mutations in mismatch repair genes and several genes of moderate penetrance are responsible for the remaining known hereditary risk. Women with a history of familial ovarian cancer or with known germline mutations in highly penetrant genes are offered the option of risk-reducing surgery that involves the removal of the ovaries and fallopian tubes (salpingo-oophorectomy). Growing evidence now supports the fallopian tube epithelia as an etiological site for the development of HGSC and consequently, salpingectomy alone is emerging as a prophylactic option. This review discusses the site of origin of EOC, the rationale for risk-reducing salpingectomy in the high-risk population, and opportunities for salpingectomy in the low-risk population.
ovarian cancer fallopian tube origin, serous tubal intraepithelial carcinoma, STIC lesion ovarian cancer precursor, opportunistic salpingectomy cancer prevention, BRCA1 BRCA2 ovarian cancer risk, high-grade serous carcinoma pathogenesis, fallopian tube fimbria cancer origin, prophylactic salpingectomy ovarian cancer, tubal origin epithelial ovarian cancer, ovarian cancer prevention salpingectomy
PMID 27200296 27200296 DOI 10.3389/fonc.2016.00108 10.3389/fonc.2016.00108
Cite this article
George, S., Garcia, R., & Slomovitz, B. (2016). Ovarian Cancer: The Fallopian Tube as the Site of Origin and Opportunities for Prevention. *Frontiers in oncology*, *6*, 108. https://doi.org/10.3389/fonc.2016.00108
George S, Garcia R, Slomovitz B. Ovarian Cancer: The Fallopian Tube as the Site of Origin and Opportunities for Prevention. Front Oncol. 2016;6:108. doi:10.3389/fonc.2016.00108
George, Sophia, et al. "Ovarian Cancer: The Fallopian Tube as the Site of Origin and Opportunities for Prevention." *Frontiers in oncology*, vol. 6, 2016, pp. 108.
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