Wang Jiayong, Zhang Zhaoyang, Xu Kesen, Sun Xiaohui, Yang Guangyun, Niu Weibo, Liu Enyu, Peng Cheng, Lin Pengfei, Wang Jian, Chen Rong, Agrez Michael, Niu Jun
Department of General Surgery, QiLu Hospital, Shandong University, Jinan, Shandong, China.
Int J Cancer. 2008 Sep 15;123(6):1311-7. doi: 10.1002/ijc.23656.
Integrin alphaupsilonbeta6 plays a very important role in the progression of colon cancer cells and is now defined as a novel, independent prognostic indicator for aggressive colon cancer in humans. Herein, we use the RNA interfering technology to downregulate the expression of alphaupsilonbeta6 in colon cancer cells. Our data demonstrate that plasmid vector based shRNA can effectively down-regulate alphaupsilonbeta6 expression in protein and mRNA levels. Supression of integrin alphaupsilonbeta6 inhibits the phosphorylation and nonphosphorylation level of ERK1/2, the secretion of uPA, pro-MMP-9 and pro-MMP-2 in tumor conditioned medium, and more important, inhibits MAPK-dependent [(3)H] labeled collagen IV degradation via the plasminogen activation cascade. Our study demonstrates in vitro that supression of integrin alphaupsilonbeta6 inhibits extracellular matrix degradation through the MAPK pathway.
整合素αvβ6在结肠癌细胞进展中发挥着非常重要的作用,目前被定义为人类侵袭性结肠癌的一种新型独立预后指标。在此,我们使用RNA干扰技术下调结肠癌细胞中αvβ6的表达。我们的数据表明,基于质粒载体的短发夹RNA(shRNA)可有效下调αvβ6在蛋白质和mRNA水平的表达。整合素αvβ6的抑制可抑制细胞外调节蛋白激酶1/2(ERK1/2)的磷酸化和非磷酸化水平、肿瘤条件培养基中尿激酶型纤溶酶原激活物(uPA)、前基质金属蛋白酶-9(pro-MMP-9)和前基质金属蛋白酶-2(pro-MMP-2)的分泌,更重要的是,通过纤溶酶原激活级联反应抑制丝裂原活化蛋白激酶(MAPK)依赖性[³H]标记的IV型胶原降解。我们的研究在体外证明,整合素αvβ6的抑制通过MAPK途径抑制细胞外基质降解。