Li Qi, Zhang Yan-Hua, Li Pei-Ling, Pei Jun-Rui
Department of Obstetrics and Gynecology, Second Affiliated Hospital of Harbin Medical University, Harbin 150081, China.
Zhonghua Fu Chan Ke Za Zhi. 2008 Mar;43(3):218-22.
To explore the inhibitory effect of integrin-linked kinase antisense oligonucleotide (ILK-ASODN) on cell proliferation in human ovarian cancer cell line (HO8910).
We transfected ILK-ASODN into HO8910 to block ILK gene expression, measured the expression levels of integrin-linked kinase (ILK) mRNA by RT-PCR and ILK protein by western-blotting; the inhibiting effects of the transfection on HO8910 proliferation, the cell cycles, and cell apoptosis were assessed by water soluble tetrazolium-1 (WST-1) and flow cytometry (FCM).
After transfection of ILK-ASODN, the expression levels of ILK mRNA decreased significantly in groups D, E, F being 0.307 +/- 0.011, 0.198 +/- 0.008, 0, respectively, when compared with those of the two control groups of A and B (P < 0.05). The expression levels of ILK protein of the groups D, E and F decreased significantly also, being 26.3 +/- 0.8, 20.6 +/- 0.4 and 0, respectively. HO8910 cell proliferation was inhibited significantly, and the rates of apoptosis of the groups D, E and F increased significantly, being 7.31%, 8.84% and 11.27% respectively. The cell population increased in G0/G1 phase of the groups D, E and F, being 49.25%, 56.28% and 67.61% respectively, significantly different in comparison with those of groups of A and B (P < 0.01).
Transfection of ILK-ASODN into human ovarian cancer line inhibited cancer cell proliferation significantly.
探讨整合素连接激酶反义寡核苷酸(ILK-ASODN)对人卵巢癌细胞系(HO8910)细胞增殖的抑制作用。
将ILK-ASODN转染至HO8910中以阻断ILK基因表达,通过逆转录聚合酶链反应(RT-PCR)检测整合素连接激酶(ILK)mRNA的表达水平,通过蛋白质免疫印迹法检测ILK蛋白水平;采用水溶性四氮唑盐-1(WST-1)和流式细胞术(FCM)评估转染对HO8910增殖、细胞周期及细胞凋亡的影响。
转染ILK-ASODN后,与A、B两个对照组相比,D、E、F组ILK mRNA表达水平显著降低,分别为0.307±0.011、0.198±0.008、0(P<0.05)。D、E、F组ILK蛋白表达水平也显著降低,分别为26.3±0.8、20.6±0.4、0。HO8910细胞增殖受到显著抑制,D、E、F组细胞凋亡率显著升高,分别为7.31%、8.84%、11.27%。D、E、F组处于G0/G1期的细胞比例增加,分别为49.25%、56.28%、67.61%,与A、B组相比差异有统计学意义(P<0.01)。
将ILK-ASODN转染至人卵巢癌细胞系可显著抑制癌细胞增殖。