Tubal and ovarian pathways to pelvic epithelial cancer: a pathological perspective.

TitleTubal and ovarian pathways to pelvic epithelial cancer: a pathological perspective.
Publication TypeJournal Article
Year of Publication2008
AuthorsJarboe EA, Folkins AK, Drapkin R, Ince TA, Agoston ES, Crum CP
JournalHistopathology
Volume53
Issue2
Pagination127-38
Date Published2008 Aug
ISSN1365-2559
KeywordsAnimals, Fallopian Tube Neoplasms, Female, Humans, Neoplasms, Glandular and Epithelial, Ovarian Neoplasms, Pelvic Neoplasms
Abstract

Prolongation of ovarian epithelial cancer survival depends on early detection or improved responses to chemotherapy. Gains in either have been modest at best. Understanding the diverse pathogenesis of this disease is critical to early intervention or prevention. This review addresses six important variables, including (i) cell of origin, (ii) site of origin, (iii) initial genotoxic events, (iv) risks imposed by hereditary and other promoting conditions, (v) subsequent factors that promote different patterns of metastatic spread, and (vi) prospects for intervention. This review proposes two distinct pathways to pelvic epithelial cancer. The first initiates in ovarian surface epithelium (OSE), Mullerian inclusions or endometriosis in the ovary. The second arises from the endosalpinx and encompasses a subset of serous carcinomas. The serous carcinogenic sequence in the distal fallopian tube is described and contrasted with lower grade serous tumors based on tumour location, earliest genetic change and ability (or lack of) to undergo terminal (ciliated) differentiation. Ultimately, a clear understanding of tumour origin and the mechanism(s) leading to the earliest phases of the serous and endometrioid carcinogenic sequences may hold the greatest promise for designing prevention strategies and/or developing new therapies.

DOI10.1111/j.1365-2559.2007.02938.x
Alternate JournalHistopathology
PubMed ID18298580
Grant List1 R21 CA124688 / CA / NCI NIH HHS / United States
1P50CA 105009 / CA / NCI NIH HHS / United States
K08 CA108748 / CA / NCI NIH HHS / United States
Related Faculty: 
Tan Ince, M.D., Ph.D.

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