Expression of steroid receptors and proteins related to apoptosis in endometria of women with polycystic ovary syndrome

Maliqueo, M; Clementi M.; Gabler F.; Johnson, MC; Palomino A.; Sir Petermann T; Vega M.

Abstract

Objective: To evaluate the expression of steroid hormone receptors, proteins related to apoptosis, and cell proliferation in endometria from women with polycystic ovary syndrome (PCOS). Design: Case-control study. Setting: Hospital research unit. Patient(s): Eight women with PCOS and 12 fertile healthy women of similar age to those with PCOS. Intervention(s): Endometrial samples were obtained from women with PCOS (PCOSE) and normal (NE) women during the proliferative phase of the menstrual cycle. Main Outcome Measure(s): Expression studies (immunohistochemistry and reverse transcription-polymerase chain reaction) and DNA fragmentation [TdT-mediated dUTP nick end labeling (TUNEL)]. Result(s): In stroma, protein expression of estrogen receptor ?, Bcl-2, and Bax was higher in PCOSE than in NE; epithelial cells had a greater expression of androgen receptor in the nucleus and a lower expression in the cytoplasm of PCOSE. Cell proliferation was higher in the epithelia of NE, while the expression of caspase-3 and DNA fragmentation was similar in both groups. The bax mRNA expression was higher in PCOSE, and bcl-2 mRNA expression was similar between groups. A higher bcl-2/bax relative ratio in PCOSE was observed. Conclusion(s): An alternating expression of proteins related to cell survival in endometria from PCOSE may potentially be associated with the disruption of their endometrial cell cycle. © 2003 by American Society for Reproductive Medicine.

Más información

Título según WOS: Expression of steroid receptors and proteins related to apoptosis in endometria of women with polycystic ovary syndrome
Título según SCOPUS: Expression of steroid receptors and proteins related to apoptosis in endometria of women with polycystic ovary syndrome
Título de la Revista: FERTILITY AND STERILITY
Volumen: 80
Número: SUPPL. 2
Editorial: Elsevier Science Inc.
Fecha de publicación: 2003
Página de inicio: 812
Página final: 819
Idioma: English
DOI:

10.1016/S0015-0282(03)00978-7

Notas: ISI, SCOPUS