Yue Wen, Sun Quanhong, Landreneau Rodney, Wu Chuanyue, Siegfried Jill M, Yu Jian, Zhang Lin
Department of Pharmacology and Chemical Biolog, University of Pittsburgh Cancer Institute, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15213, USA.
Cancer Res. 2009 Aug 1;69(15):6339-46. doi: 10.1158/0008-5472.CAN-09-0398. Epub 2009 Jul 7.
The high mortality rate of lung cancer is largely due to the spread of disease to other organs. However, the molecular changes driving lung cancer invasion and metastasis remain unclear. In this study, we identified fibulin-5, a vascular ligand for integrin receptors, as a suppressor of lung cancer invasion and metastasis. Fibulin-5 was silenced by promoter hypermethylation in a majority of lung cancer cell lines and primary tumors. It inhibited lung cancer cell invasion and down-regulated matrix metalloproteinase-7 (MMP-7), which promoted lung cancer cell invasion. Knockdown of fibulin-5 was sufficient to stimulate cell invasion and MMP-7 expression. The expression levels of fibulin-5 and MMP-7 were inversely correlated in lung tumors. Suppression of MMP-7 expression by fibulin-5 was mediated by an integrin-binding RGD motif via the extracellular signal-regulated kinase (ERK) pathway. Furthermore, overexpression of fibulin-5 in H460 lung cancer cells inhibited metastasis in mice. Collectively, these results suggest that epigenetic silencing of fibulin-5 promotes lung cancer invasion and metastasis by activating MMP-7 expression through the ERK pathway.
肺癌的高死亡率很大程度上归因于疾病扩散至其他器官。然而,驱动肺癌侵袭和转移的分子变化仍不清楚。在本研究中,我们确定整合素受体的血管配体纤连蛋白-5是肺癌侵袭和转移的抑制因子。在大多数肺癌细胞系和原发性肿瘤中,纤连蛋白-5因启动子高甲基化而沉默。它抑制肺癌细胞侵袭并下调促进肺癌细胞侵袭的基质金属蛋白酶-7(MMP-7)。敲低纤连蛋白-5足以刺激细胞侵袭和MMP-7表达。在肺肿瘤中,纤连蛋白-5和MMP-7的表达水平呈负相关。纤连蛋白-5对MMP-7表达的抑制作用是通过整合素结合RGD基序经细胞外信号调节激酶(ERK)途径介导的。此外,在H460肺癌细胞中过表达纤连蛋白-5可抑制小鼠体内的转移。总体而言,这些结果表明,纤连蛋白-5的表观遗传沉默通过ERK途径激活MMP-7表达,从而促进肺癌的侵袭和转移。