The growth hormone-releasing hormone (GHRH) antagonist JV-1-36 inhibits proliferation and survival of human ectopic endometriotic stromal cells (ESCs) and the T HESC cell line

被引:16
作者
Annunziata, Marta [1 ]
Grande, Cristina [1 ]
Scarlatti, Francesca [1 ]
Deltetto, Francesco [2 ]
Delpiano, Elena [2 ]
Camanni, Marco [2 ]
Ghigo, Ezio
Granata, Riccarda [1 ]
机构
[1] Univ Turin, Lab Mol & Cellular Endocrinol, Div Endocrinol & Metab, Dept Internal Med, I-10126 Turin, Italy
[2] Unit Minimally Invas Gynecol, Ginteam, Turin, Italy
关键词
Endometriosis; growth hormone-releasing hormone (GHRH); GHRH receptor (GHRH-R); GHRH antagonists; SPLICE VARIANTS; CANCER CELLS; IN-VITRO; IGF-II; PANCREATIC-CANCER; PROSTATE CANCERS; PITUITARY-CELLS; LUNG-CARCINOMA; PROTEIN-KINASE; MESSENGER-RNA;
D O I
10.1016/j.fertnstert.2009.03.093
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: To determine the effect of the GHRH antagonist JV-1-36 on proliferation and survival of primary ectopic human endometriotic stromal cells (ESCs) and the T HESC cell line. Design: Prospective laboratory study. Setting: University hospital. Patient(s): 22 women with endometriosis (aged 34.8 +/- 5.7 years) undergoing therapeutic laparoscopy. Intervention(s): Eutopic (n=10) and ectopic (n=22) endometrial tissues were collected from women who underwent therapeutic laparoscopic surgery for endometriosis (stage III/IV). Main Outcome Measure(s): Expression of GHRH, GHRH receptor (GHRH-R) and GHRH-R splice variant (SV) 1 mRNA was determined by reverse-transcription polymerase chain reaction (RT-PCR). The ESC proliferation was assessed by 5-bromo-2-deoxyuridine incorporation, cell survival by 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazolium bromide (MTT) and Trypan blue assay. The T HESC survival was evaluated by MTT, cyclic adenosine monophosphate (cAMP) levels by ELISA, extracellular signal-regulated kinases 1 and 2 (ERK1/2) phosphorylation by Western blot, and insulin-like growth factor (IGF)-2 mRNA by real-time PCR. Result(s): The ESCs and T HESCs, but not normal endometrial tissues, expressed GHRH-R mRNA; SV1 mRNA was determined in normal endometrial tissues, ESCs, and T HESCs; GHRH mRNA was found in T HESCs; JV-1-36 inhibited ESC proliferation and ESC and T HESC survival. In T HESCs, JV-1-36 reduced cAMP production and ERK1/2 phosphorylation but had no effect on IGF-2 mRNA expression. Conclusion(s): The GHRH antagonist JV-1-36 inhibits endometriotic cell proliferation and survival, suggesting that GHRH antagonist may represent promising tools for treatment of endometriosis. (Fertil Steril (R) 2010; 94: 841-9. (c) 2010 by American Society for Reproductive Medicine.)
引用
收藏
页码:841 / 849
页数:9
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