Gu Yan, Chen Ji-sheng, Zhou Xiao-dong
Department of Surgery, Ninth People's Hospital, Shanghai Second Medical University, Shanghai 200011, China.
Zhonghua Gan Zang Bing Za Zhi. 2003 Oct;11(10):612-5.
To study the inhibitory effects of antisense focal adhesion kinase (FAK) oligodeoxynucleotides (ODN) on the invasion of Bel 7402 cells, and investigate the mechanisms.
LipofecTAMINE-mediated antisense FAK ODN was transfected into Bel 7402 cells. Cell number and viability were evaluated every 24 hours by trypan blue dye exclusion. Cell attachment assay was carried out at intended time points in a microculture well pre-coated with fibronectin (FN). The invasive activity of tumor cells was assayed in a transwell cell culture chamber. Cell cycle and cell apoptosis analysis were performed with flow cytometry (FCM).
The expression of p125FAK in the group treated with antisense FAK ODN (6.49%+/-0.10%) significantly decreased, compared with those in the group treated with sense FAK ODN (14.33%+/-1.88%) and control group (16.68%+/-1.62%), F=7.66, P<0.01. Antisense FAK ODN significantly inhibited the growth of Bel 7402 cells by 30%-60%, the attachment by 25%-55%, and the invasion, 15%-25%. The decreased expression of FAK in Bel 7402 cells caused a G2/M cell cycle arrest, and the cells at S phase decreased significantly. The occurrence of apoptosis detected by FCM increased significantly in the group treated with antisense FAK ODN.
Inhibition of FAK expression significantly decreases the attachment between ECM and Bel 7402 cells, and the ability of Bel 7402 cells to invade the reconstituted basement membrane. In addition, FAK suppression significantly inhibits the proliferation of Bel 7402 cells in vitro, and increases their apoptosis.
研究反义粘着斑激酶(FAK)寡脱氧核苷酸(ODN)对Bel 7402细胞侵袭的抑制作用,并探讨其机制。
采用脂质体介导的方法将反义FAK ODN转染至Bel 7402细胞。每24小时通过台盼蓝拒染法评估细胞数量和活力。在预先包被纤连蛋白(FN)的微孔培养板中于预定时间点进行细胞贴壁试验。在Transwell细胞培养小室中检测肿瘤细胞的侵袭活性。采用流式细胞术(FCM)进行细胞周期和细胞凋亡分析。
与正义FAK ODN处理组(14.33%±1.88%)和对照组(16.68%±1.62%)相比,反义FAK ODN处理组中p125FAK的表达(6.49%±0.10%)显著降低,F=7.66,P<0.01。反义FAK ODN显著抑制Bel 7402细胞生长30%-60%,贴壁25%-55%,侵袭15%-25%。Bel 7402细胞中FAK表达降低导致G2/M期细胞周期阻滞,S期细胞显著减少。FCM检测显示,反义FAK ODN处理组细胞凋亡发生率显著增加。
抑制FAK表达可显著降低细胞外基质与Bel 7402细胞之间的粘附,以及Bel 7402细胞侵袭重组基底膜的能力。此外,抑制FAK可显著抑制Bel 7402细胞体外增殖,并增加其凋亡。