Aging and Development of Ovarian Epithelial Carcinoma: The Relevance of Changes in Ovarian Stromalandrogen Production
- 66 Downloads
There are three types of ovarian neoplasms: (1) Those which arise from the surface epithelium covering the ovary. (2) Those which are derived from the cortical mesenchymal stroma. (3) Those which develop from germ cells. Our laboratory has concentrated its effort on solid tumors in women of the first type, epithelial, which has the highest incidence and is the most lethal. Development of these tumors is correlated with aging in the ovary. They form primarily during the perimenopause. Among women, 64% of the total ovarian cancer cases are diagnosed between ages 41 and 60 years1. Our approach has been to establish stable tumor cell lines from patient specimens for use as in vitro models. We have investigated the response of these cells to steroid hormones because we hypothesized that these tumors retain some metabolic characteristics which are specific to the ovary. Our data demonstrate that testosterone and androstenedione, but not cortisol, inhibited proliferation of ovarian tumor cells in vitro by a mechanism which was independent of steroid receptors. These androgens are routinely synthesized and secreted by human ovary, and in the menopausal ovary the primary source of androgen is the stromal cell compartment. Because a relatively high local concentration of ovarian androgen exists in vivo, it is possible that androgen may suppress ovarian epithelial carcinoma in women as well. If it does, then development of this carcinoma may be facilitated when the postmenopausal ovary fails to produce adequate androgen during postreproductive years.
KeywordsOvarian Cancer Ovarian Carcinoma Ovarian Cancer Cell Ovarian Cancer Cell Line Borderline Tumor
Unable to display preview. Download preview PDF.
- 1.Zaloudek, C. The Ovary. In: Gompel, C. and S. G. Silverberg, S. G. (eds.) Pathology In Gynecology And Obstetrics. J. B. Lippincott Company, Philadelphia (1985).Google Scholar
- 2.Young, J. L., Jr., Percy, C. L. and Asire, A. J. “Surveillance, epidemiology and end results: incidence and mortality data”, 1973–1977. National Cancer Institute Monograph 57, DHHS no. (NIH) 81–2330. U. S. Government Printing Office, Washington, DC. pp 50-51 (1981).Google Scholar
- 10.Slotman, B. J. Rationale For The Use Of Endocrine Therapy In Ovarian Cancer. Thesis Publishers, Amsterdam (1990).Google Scholar
- 18.McNatty, K. P., Smith, D. M., Makris, A., DeGrazia, D. Tulchinsky, C., Osathanondh, R., Schiff, I. and Ryan, K. J. The intraovarian sites of androgen and estrogen formation in women with normal and hyperadrogenic ovaries as judged by in vitro experiments. J. Clin. Endocrinol. Metab. 50:755 (1980).PubMedCrossRefGoogle Scholar