Yin H, Cheng K W, Hwa H L, Peng C, Auersperg N, Leung P C
Department of Obstetrics and Gynaecology, University of British Columbia, Vancouver, Canada.
Life Sci. 1998;62(22):2015-23. doi: 10.1016/s0024-3205(98)00173-8.
The presence of gonadotropin-releasing hormone (GnRH) binding sites in biopsy samples of human epithelial ovarian cancer and ovarian tumor cell lines as well as the demonstration of the inhibitory effects of GnRH analogues on the growth of these cells raised the possibility that GnRH is produced locally by ovarian cancer cells. In order to investigate an autocrine/paracrine regulatory mechanism in human carcinomas, we have studied the expression of GnRH and GnRHR mRNA in human ovarian epithelial cell lines (OVCAR-3 and SKOV-3), human choriocarcinoma cell line (JEG-3) and human hepatocarcinoma cell line (HepG 2). Using primers corresponding to published human GnRH and GnRHR cDNA sequences, predicted PCR products were obtained from these cell lines by reverse transcription-polymerase chain reaction (RT-PCR) and confirmed by Southern hybridization. Sequencing analysis of GnRH PCR products showed that their sequences have 100% identity to the published human GnRH cDNA sequence. These results indicated that GnRH and GnRHR genes are expressed in all the cell lines tested in the present study, and strengthen the concept that GnRH may act as an autocrine regulator on the growth of cancer cells.
在人上皮性卵巢癌活检样本和卵巢肿瘤细胞系中存在促性腺激素释放激素(GnRH)结合位点,以及GnRH类似物对这些细胞生长具有抑制作用,这提示GnRH可能由卵巢癌细胞在局部产生。为了研究人类癌症中的自分泌/旁分泌调节机制,我们研究了GnRH和GnRHR mRNA在人卵巢上皮细胞系(OVCAR-3和SKOV-3)、人绒毛膜癌细胞系(JEG-3)和人肝癌细胞系(HepG 2)中的表达。使用与已发表的人GnRH和GnRHR cDNA序列对应的引物,通过逆转录-聚合酶链反应(RT-PCR)从这些细胞系中获得了预测的PCR产物,并通过Southern杂交进行了证实。GnRH PCR产物的测序分析表明,其序列与已发表的人GnRH cDNA序列具有100%的同一性。这些结果表明,GnRH和GnRHR基因在本研究中测试的所有细胞系中均有表达,并强化了GnRH可能作为癌细胞生长的自分泌调节因子的概念。