Yuan Cai-Xia, Gu Shuang, Zhang Shu-Hong, Zhang Xiang-Ning
Department of Obstetrics and Gynecology, Qilu Hospital of Shandong University, Jinan 250012, China.
Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2008 Dec;30(6):711-6.
To investigate the heparitinase (HPA) expression and cell invasiveness in human ovarian cancer cell line SKOV3 during hypoxia, and explore their relationship with hypoxia inducible factor-1alpha (HIF-1alpha).
SKOV3 cells were incubated with normoxia, hypoxia, and hypoxia plus rapamycin, respectively. SKOV3 cells of hypoxia group were incubated in 5% CO2 + 1% O2. Cells in hypoxia plus rapamycin group were incubated with 10 ng/ml of rapamycin before cultured under hypoxic condition. Cells in each group were collected for analysis after incubated with hypoxia for 12, 24, and 36 hours, respectively. Western blotting and RT-PCR were performed to detect the expressions of HIF-1alpha and HPA. Cell invasiveness was measured by matrigel invasion assay.
Western blotting showed that the expression of HIF-1alpha significantly increased compared with normoxic group (P < 0.05). However, hypoxia had no obvious impact on HIF-1alpha mRNA expression. The expressions of HPA protein and mRNA of SKOV3 cells of hypoxia group were significantly higher than normoxic group (P < 0.05). The up-regulation of HPA expression in hypoxic group decreased after the utilization of rapamycin. The cell invasion of hypoxic group was significantly higher than that of normoxic group (P < 0.05); meanwhile, the expression of HPA was positively correlated with the invasiveness of SKOV3 cells (r = 0.9863, P < 0.05).
Hypoxia may promote the expression of HPA and the invasiveness of SKOV3 cells through the HIF-1alpha pathway, which plays an important role in the pathogenesis of ovarian cancer.
研究缺氧状态下人卵巢癌细胞系SKOV3中乙酰肝素酶(HPA)的表达及细胞侵袭能力,并探讨其与缺氧诱导因子-1α(HIF-1α)的关系。
分别将SKOV3细胞置于常氧、缺氧及缺氧加雷帕霉素环境中培养。缺氧组细胞在5%二氧化碳+1%氧气环境中培养。缺氧加雷帕霉素组细胞在缺氧培养前先加入10 ng/ml雷帕霉素。分别在缺氧培养12、24和36小时后收集各组细胞进行分析。采用蛋白质免疫印迹法(Western blotting)和逆转录-聚合酶链反应(RT-PCR)检测HIF-1α和HPA的表达。通过基质胶侵袭实验检测细胞侵袭能力。
蛋白质免疫印迹法显示,与常氧组相比,缺氧组HIF-1α表达显著增加(P<0.05)。然而,缺氧对HIF-1α mRNA表达无明显影响。缺氧组SKOV3细胞HPA蛋白及mRNA表达均显著高于常氧组(P<0.05)。使用雷帕霉素后,缺氧组HPA表达上调程度降低。缺氧组细胞侵袭能力显著高于常氧组(P<0.05);同时,HPA表达与SKOV3细胞侵袭能力呈正相关(r = 0.9863,P<0.05)。
缺氧可能通过HIF-1α途径促进HPA表达及SKOV3细胞侵袭能力,这在卵巢癌发病机制中起重要作用。