In vitro effects of gonadotropin-releasing hormone (GnRH) analogue on cancer cell sensitivity to cis-platinum

被引:28
作者
Ohta, H [1 ]
Sakamoto, H [1 ]
Satoh, K [1 ]
机构
[1] Nihon Univ, Sch Med, Dept Obstet & Gynecol, Itabashi Ku, Tokyo 1738610, Japan
关键词
gonadotropin-releasing hormone agonist; endometrial cancer; ovarian cancer; human telomerase;
D O I
10.1016/S0304-3835(98)00270-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Six endometrial cancer cell lines (Ishikawa, EIIL, HEC1A, 6, 50 and 59), one breast cancer cell line (MCF7) and two ovarian cancer cell lines (OVHS-1, HRA) were treated for 24 or 168 h with a gonadotropin-releasing hormone (GnRH) analogue, Buserelin acetate, and the cellular growth profile was studied. All these cell lines except for the HRA Line had positive GnRH receptor mRNA expression detected by reverse transcriptase polymerase chain reaction. GnRHa suppressed cell growth after 168 I;of exposure, but not after 24 h. Suppression of cell growth by the exposure to cis-platinum (CDDP, 10 nM for 24 h) was significantly increased in the presence of GnRHa for 168 h. The mechanism of this growth inhibition was tested by examining both RNA components of human telomerase (hTR) expression and telomerase activity. The results showed that GnRHa inhibits telomerase activity without altering the RNA component of telomerase expression. The present data suggest that GnRH analogue may modulate endometrial, breast and ovarian cancer cell growth through modifying the telomerase activity. Since GnRHa increased the cytotoxic effects of CDDP and GnRHa is a compound of high patient compliance, the value of GnRHa as a tumor sensitizer to CDDP should be further tested in clinical trials. (C) 1998 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:111 / 118
页数:8
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