ESTROGEN STIMULATION OF OVARIAN SURFACE EPITHELIAL CELL PROLIFERATION

• Published in: In vitro cellular & developmental biology. Animal 2000-11, Vol.36 (10), p.657-666
• Main Authors: BAI, WENLONG, OLIVEROS-SAUNDERS, BEATRIZ, WANG, QIANG, ACEVEDO-DUNCAN, MILDRED E, NICOSIA, SANTO V
• Format: Article
• Language: English
• Subjects: Animals; Cell Division - drug effects; Cell growth; CELL GROWTH/DIFFERENTIATION/APOPTOSIS; Cultured cells; Epithelial cells; Epithelial Cells - drug effects; Epithelial Cells - metabolism; estrogen receptor; Estrogens; Estrogens - pharmacology; Female; Granulosa cells; Hormones; Immunohistochemistry; Interstitial cells; ovarian cancer; ovarian surface epithelium; Ovaries; Ovary - cytology; Ovary - drug effects; Ovary - metabolism; Papillae; proliferation; Rabbits; Receptors, Estrogen - metabolism; Stromal cells; stromal–epithelial interactions
• ISSN: 1071-2690; 1543-706X; 1543-706X
• DOI: 10.1290/1071-2690(2000)036<0657:ESOOSE>2.0.CO;2

Ovarian cancer is the leading cause of gynecological cancer mortality, and 85–90% of this malignancy originates from the ovarian surface epithelium (OSE). The etiology of ovarian epithelial cancer is unknown, but a role for estrogens has been suspected. However, the effect of estrogens on OSE cell proliferation remains to be determined. Using the rabbit model, our studies have demonstrated that 17β-estradiol stimulates OSE cell proliferation and the formation of a papillary ovarian surface morphology similar to that seen in human ovarian serous neoplasms of low malignant potential. Immunohistochemical staining of ovarian tissue sections with an antibody to the estrogen receptor α demonstrates its expression in both OSE cells and stromal interstitial cells. In primary ovarian cell cultures, the proliferative response of the epithelial cells to 17β-estradiol depends on the expression of the estrogen receptor α in the epithelial cells. However, when the epithelial cells are grown together with ovarian stromal cells, their proliferative response to this hormone is greatly enhanced, suggesting the involvement of stromal–epithelial interactions. These studies suggest a role for estrogens and the estrogen receptor α in OSE growth.