Laboratory of Experimental Cancerology, Ghent University Hospital, Ghent, Belgium.
CNRS UMR 7098, Paris.
Int J Oncol. 2011 Aug;39(2):393-400. doi: 10.3892/ijo.2011.1034. Epub 2011 May 9.
We have previously shown that the genotoxin-induced apoptosis in mouse embryo fibroblasts was enhanced by the extracellular matrix protein fibronectin (FN). In the present study, we tested the hypothesis that FN regulates the DNA damage response (DDR) signaling pathways in HCT116 (p53-wt) and HT29 (p53-mut) human colon cancer cells and tumor-derived myofibroblasts. DNA damage recognition mechanisms were analyzed by immunofluorescence staining, cell cycle analysis and immunoblotting addressed at specific molecular sensors and executors involved in the DDR pathways. The results show that FN, but not collagen type IV or Matrigel, initiates and potentiates the DDR to the anticancer drug cisplatin in an α5 integrin and cell cycle-dependent manner (S and G2/M phases) in human colon cancer cells. Accordingly, we demonstrate that adhesion of HCT116 cells to FN upregulated the expression of α5 integrin FN receptors at the cell surface. These FN-induced DDR pathways include the concerted phosphorylation of histone H2AX on Ser139 detected as nuclear foci (γ-H2AX, 15 and 25 kDa forms), of ataxia telangiectasia mutated (ATM-Ser1981), checkpoint kinase 2 (CHK2-Thr68, 62 and 67 kDa) and p53-Ser15. These FN-induced γ-H2AX signals were interrupted or attenuated by selective inhibitors acting on the DDR pathway kinases, including wortmannin (targeting the phosphatidylinositol-3-kinase-related protein kinases, PIKK), KU55933 (ATM), NU7026 (DNA-dependent protein kinase catalytic subunit, DNA-PK-cs) and SP600125 (JNK2, stress activated protein kinase/c-Jun N-terminal kinase-2). Adhesion to FN also potentiated the γ-H2AX signals and the cytotoxic effects of cisplatin in human colon tumor-derived myofibroblasts. These data provide evidence that FN promotes DNA damage recognition and chemosensitization to cisplatin via the potentiation of the DNA damage signaling responses in human colon cancer cells and tumor-derived myofibroblasts.
我们之前已经证明,细胞外基质蛋白纤维连接蛋白(FN)可以增强基因毒性诱导的小鼠胚胎成纤维细胞凋亡。在本研究中,我们检验了以下假设:FN 调节 HCT116(野生型 p53)和 HT29(突变型 p53)人结肠癌细胞和肿瘤衍生的肌成纤维细胞中的 DNA 损伤反应(DDR)信号通路。通过免疫荧光染色、细胞周期分析和免疫印迹分析,检测 DDR 通路中特定的分子传感器和执行者,分析 DNA 损伤识别机制。结果表明,FN(而非胶原 IV 或 Matrigel)以 α5 整合素和细胞周期依赖性方式(S 和 G2/M 期)起始并增强人结肠癌细胞对抗癌药物顺铂的 DDR。因此,我们证明 HCT116 细胞黏附到 FN 可上调细胞表面 FN 受体α5 整合素的表达。这些 FN 诱导的 DDR 通路包括在核斑点(γ-H2AX,15 和 25 kDa 形式)上检测到的组蛋白 H2AX 丝氨酸 139 的协同磷酸化,以及共济失调毛细血管扩张突变(ATM-Ser1981)、检查点激酶 2(CHK2-Thr68、62 和 67 kDa)和 p53-Ser15。这些 FN 诱导的 γ-H2AX 信号被选择性作用于 DDR 通路激酶的抑制剂阻断或减弱,包括渥曼青霉素(针对磷脂酰肌醇-3-激酶相关蛋白激酶,PIKK)、KU55933(ATM)、NU7026(DNA 依赖性蛋白激酶催化亚基,DNA-PK-cs)和 SP600125(JNK2、应激激活蛋白激酶/c-Jun N 末端激酶-2)。黏附到 FN 也增强了 γ-H2AX 信号和人结肠肿瘤衍生的肌成纤维细胞中顺铂的细胞毒性作用。这些数据提供了证据,表明 FN 通过增强人结肠癌细胞和肿瘤衍生的肌成纤维细胞中的 DNA 损伤信号反应,促进 DNA 损伤识别和对顺铂的化学增敏作用。