Insulin-like growth factor-II participates in the biphasic effect of a gonadotropin-releasing hormone agonist on ovarian cancer cell growth

被引:27
|
作者
Ho, MN [1 ]
Delgado, CH [1 ]
Owens, GA [1 ]
Steller, MA [1 ]
机构
[1] NCI, SURG BRANCH, GYNECOL ONCOL SECT, BETHESDA, MD 20892 USA
关键词
IGF-II; tryptorelin; biphasic; ovarian cancer;
D O I
10.1016/S0015-0282(97)81399-4
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: To examine the involvement of insulin-like growth factors (IGFs) in growth regulation of an ovarian cancer cell line and to investigate whether the GnRH agonist tryptorelin might influence a potential autocrine or paracrine loop involving IGFs. Design: In vitro, prospective, randomized controlled study. Setting: In vitro experiments at the Section of Gynecologic Oncology, Surgery Branch, National Cancer Institute. Patient(s): None. Human ovarian adenocarcinoma cell line IGROV-1. Intervention(s): The proliferative effect of tryptorelin on IGROV-1 cells was analyzed by using the MTT (93-(4,5-dimethylthiazol-2-yl)2,5-diphenyl tetrazolium bromide) colorimetric assay. The ribonuclease protection assay was used to investigate whether an autocrine pathway involving IGF-I or IGF-II might participate in the growth of these cells. The expression of GnRH receptor was assessed by the I-125-GnRH binding assay. Main Outcome Measure(s): Changes in cell growth and expression of IGF-I and IGF-II messenger RNA (mRNA). Result(s): Tryptorelin exhibited a bimodal, dose- and time-dependent effect on IGROV-1 cells when compared with untreated control cells: Cellular proliferation was enhanced during the first 24 hours of exposure, but longer incubations resulted in growth inhibition. The mitogenic effect of tryptorelin was inhibited when cells were co-incubated with either IGF binding protein-5 (IGFBP-5) or anti-IGF-II antibody, which can both bind to IGF-II and neutralize it. Insulinlike growth factor-I mRNA was not detected in IGROV-1 cells. However, IGF-II transcripts were detected after incubation with tryptorelin for 12 hours, but thereafter, no mRNA was observed, even after prolonged exposure. Binding analysis revealed a specific, high-affinity GnRH binding site. Conclusion(s): These data suggest that tryptorelin exerts a bimodal growth effect on ovarian cancer cells by a mechanism involving the autocrine production of IGF-II. The effect of tryptorelin on IGF-II gene transcription in these ovarian cancer cells appears to mirror the desensitizing effects of prolonged GnRH exposure on pituitary gonadotropin production. (C) 1997 by American Society for Reproductive Medicine.
引用
收藏
页码:870 / 876
页数:7
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