目的:探讨促性腺激素及核转录因子-κB(NF-κB)对卵巢癌细胞增殖的影响。方法:不同剂量的人重组促性腺激素与卵巢癌细胞株OVCAR-3、Caov-3共培养,应用四甲基偶氮唑蓝(MTT)实验观测其对卵巢癌细胞生长的影响,同时应用RT—PCR和ELISA方法检测卵巢癌细胞NF-κB水平,以分析其信号传导途径。结果:2种促性腺激素对卵巢癌细胞株均有促增殖作用,分别增加35%-202%(P〈0.05);68%~192%(P〈0.01),并使细胞内NF-κB亚单位表达增加1.53~3.98倍(P〈0.05);1.5-2.5倍(P〈0.01),与对照组相比差异具有显著性。在处理组卵巢癌细胞培养液中加入NF-κB抑制剂吡咯烷二硫代氨基甲酸盐(PDTC),上述2种卵巢癌细胞株的增殖均有所减慢。结论:促性腺激素对卵巢癌细胞株的促增殖过程可能由NF-κB介导,共同影响卵巢癌细胞的生长。
Objective: To investigate the effects and the primary mechanisms of gonadotropin and nuclear factor kappa B (NF-κB) on proliferation of human ovarian epithelial cancer cells. Methods: Two epithelial ovarian carcinoma cell lines (OVCAR-3, Caov-3) were co-cultured with follicle-stimulating hormone (FSH) or luteinizing hormone (LH) respectively. The degree of proliferation of the two cell lines was detected by MTT assay. The expression of mRNA and protein of NF-κB in cells were determined by RT- PCR and ELISA. Results: A dose-dependant effect was seen with gonadotropins in OVCAR-3 and Caov-3 (35%-202% ,P 〈0.05 ; 68%-192% ,P 〈0.01 respectively ). The levels of expression of NF-κB mRNA and protein were also increased in these two kinds of cells ( 1.53±3.98 fold, P 〈0.05 ; 1.5-2.5 fold,P 〈0.01 respectively)by FSH and LH for a period of 96 h (P〈0.05 vs. control group). Most significantly, for both cell lines, 100 μmol/L NF-κB inhibitor (PDTC) partially inhibited the hormones-stimulated cell proliferation. Conclusion: The results suggest NF-κB is possibly responsible for gonadotropins-stimulated proliferation of ovarian cancer cells.