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作 者:吴凌[1] 魏桠楠[1] 杨婷[1] 周冬梅[1] 祝颖[1] 冯怡雯[1] 张箴波[1] 祝亚平[1] 丰有吉[1]
机构地区:[1]上海交通大学附属上海市第一人民医院,上海200080
出 处:《现代生物医学进展》2011年第16期3030-3033,共4页Progress in Modern Biomedicine
基 金:国家自然科学基金(81001155和81020108027);上海市卫生局面上项目(2009028)
摘 要:目的:研究促卵泡激素(FSH)结合片段对卵巢上皮性细胞癌细胞株hey增殖活性的影响。方法:应用卵巢上皮性细胞癌细胞株hey作为实验对象,分别加入FSH、FSH结合片段、FSH+FSH结合片段。用四甲基偶氮唑蓝(MTT)法检测卵巢癌hey细胞的生长状况,Western blot检测cyclinD1、Akt、pAkt分子的表达。结果:FSH对卵巢癌hey细胞的生长有明显的促进作用,细胞生长活性提高21%。FSH结合片段对卵巢癌细胞的生长有明显抑制作用,对细胞平均抑制率为22%,且能下调cyclinDI的表达,在2.5×10^(-9)Mol/L达70%。FSH结合片段对FSH有竞争抑制作用,细胞抑制率为18%,能抑制FSH上调cyclinD1的作用,抑制率为61%。FSH能上调pAkt的表达,对Akt的表达没有明显影响,在40mIU/ml的浓度时pAkt/Akt上调率达224%。FSH结合片段对Akt的表达没有明显影响,但能明显下调pAkt的表达,且呈时间依赖性(在1 5分钟时达66%)和剂量依赖性(在2.5×10^(-9)Mol/L达31%)。FSH结合片段能抑制FSH上调pAkt的作用,抑制率为80%。结论:FSH结合片段可通过抑制FSH诱导的PI3K/Akt-cycl-inD1信号通路进而抑制上皮性卵巢癌hey细胞的增殖活性。Objective: To observe the inhibit effect of follicle-stimulating hormone (FSH) synthetic peptides (FSH binding Fragment) on the human epithelial ovarian cancer cell. Methods: Human epithelial ovarian cancer cell line hey was incubated with FSH, FSH binding fragrnent,FSH and FSH binding fragment respectively.The cell proliferation was detected by methyl thiazolyl tetrazolium (MTT) techniquel.cyclinD 1 ,Akt,pAkt were detected by western blot. Results: The proliferation of hey was increased apparently by FSH in a dose-dependent manner and the rate of proliferation average value 21% .Follicle-stimulating hormone (FSH) synthetic peptides inhibited the growth activity of hey,the rate of inhibition average value 22%.And the expression of cyclinD 1 was also inhibited up70% at the concentration of 2.5×10^-9 Mol/L.Follicle-stimulating hormone (FSH) synthetic peptides inhibited the effect of FSH on hey,included the growth activity (18%)and the expression of cyclinD1 (61%).FSH did not have effect on Akt,but pAkt was increased apparently,and pAkt/Akt was elvated 224% at the concentration of 40mlU/ml.Follicle-stimulating hormone (FSH) synthetic peptides decreased the pAkt in a time-dependent manner(almost 31% at 15 minutes) and in a dose-dependent manner(almost 66% at 2.5×10^-9 Mol/L) ,but it also did not have effect on Akt. Follicle-stimulating hormone(FS;H) synthetic peptides could inhibit the effect of FSH on pAkt(80%) .Conclusions: It is suggested that FSH binding fragment can inhibit the proliferation of ovarian cancer cell stimulated by FSH though the PI3K/Akt-cyclinD 1 pathway.
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