Kleinman D, Douvdevani A, Schally A V, Levy J, Sharoni Y
Department of Clinical Biochemistry, Faculty of Health Sciences, Ben-Gurion University of the Negev, Soroka Medical Center of Kupat Holim, Beer-Sheva, Israel.
Am J Obstet Gynecol. 1994 Jan;170(1 Pt 1):96-102. doi: 10.1016/s0002-9378(94)70391-4.
Our objective was to study the direct action of the gonadotropin-releasing hormone antagonist SB-75 and the agonist buserelin on the proliferation of endometrial cancer cells.
Two human endometrial cell lines that differ in histologic subtype and estrogen receptor content were treated with gonadotropin-releasing hormone analog. We measured the number of viable cells, cell cycle parameters, and apoptotic processes.
Growth of the Ishikawa cells was inhibited by SB-75 in a dose-dependent manner. 17 beta-Estradiol partially abolished the inhibitory effect of SB-75. The growth of the HEC-1A cells was not affected by the antagonist. Neither endometrial cancer cell line showed significant sensitivity to the agonist buserelin. Tenfold concentration of the gonadotropin-releasing hormone agonist did not abolish the inhibitory effect of the antagonist on cell growth. The growth inhibition was not associated with any change in cell cycle parameters but was associated with an induction of apoptosis.
The gonadotropin-releasing hormone antagonist SB-75 directly inhibits the growth of some human endometrial cancer cells and thus may be suitable for the treatment of endometrial tumors.
我们的目的是研究促性腺激素释放激素拮抗剂SB - 75和激动剂布舍瑞林对子宫内膜癌细胞增殖的直接作用。
用促性腺激素释放激素类似物处理两种在组织学亚型和雌激素受体含量上不同的人子宫内膜细胞系。我们测量了活细胞数量、细胞周期参数和凋亡过程。
SB - 75以剂量依赖性方式抑制了石川细胞的生长。17β - 雌二醇部分消除了SB - 75的抑制作用。HEC - 1A细胞的生长不受拮抗剂影响。两种子宫内膜癌细胞系对激动剂布舍瑞林均未显示出明显敏感性。促性腺激素释放激素激动剂浓度增加10倍并未消除拮抗剂对细胞生长的抑制作用。生长抑制与细胞周期参数的任何变化无关,但与凋亡诱导有关。
促性腺激素释放激素拮抗剂SB - 75直接抑制某些人子宫内膜癌细胞的生长,因此可能适用于子宫内膜肿瘤的治疗。