Ma Yu, Lu Bingjian, Ruan Wenjing, Wang Hongqiang, Lin Jie, Hu Hu, Deng Hong, Huang Qiong, Lai Maode
Department of Pathology, School of Medicine, Zhejiang University, Hangzhou, Zhejiang, 310058, China.
Exp Mol Pathol. 2008 Oct;85(2):141-5. doi: 10.1016/j.yexmp.2008.04.005. Epub 2008 May 11.
Insulin-like growth factor binding protein-related protein 1 (IGFBP-rP1) is a potential tumor suppressor gene. This study attempted to explore a potential senescence-like role for IGFBP-rP1 in suppressing human colorectal cancer. Recombinant IGFBP-rP1 inhibited cell proliferation and induced G1 cell cycle arrest in RKO and CW2 cells. It induced a senescence-like phenotype by showing 2-fold higher beta-galactosidase activity in IGFBP-rP1-transfectants over that in control cells. Western blot confirmed down-regulation of phosphorylated retinoblastoma protein (pRB) and up-regulation of p53 in IGFBP-rP1-transfectants as compared with control cells. Thus, IGFBP-rP1 might be a key molecule in the cellular senescence pathway. Our results uncovered a novel molecular mechanism involving the altered expression of pRB and p53 for tumor suppressor gene IGFBP-rP1 in colorectal cancer. Restoration of IGFBP-rP1 function might have potential therapeutic significance in colorectal cancer.
胰岛素样生长因子结合蛋白相关蛋白1(IGFBP-rP1)是一种潜在的肿瘤抑制基因。本研究试图探索IGFBP-rP1在抑制人类结直肠癌中潜在的类似衰老的作用。重组IGFBP-rP1抑制RKO和CW2细胞的增殖并诱导G1期细胞周期停滞。与对照细胞相比,IGFBP-rP1转染细胞中β-半乳糖苷酶活性高出2倍,表明其诱导了类似衰老的表型。蛋白质印迹法证实,与对照细胞相比,IGFBP-rP1转染细胞中磷酸化视网膜母细胞瘤蛋白(pRB)表达下调,p53表达上调。因此,IGFBP-rP1可能是细胞衰老途径中的关键分子。我们的研究结果揭示了一种新的分子机制,即结直肠癌中肿瘤抑制基因IGFBP-rP1通过改变pRB和p53的表达发挥作用。恢复IGFBP-rP1的功能可能对结直肠癌具有潜在的治疗意义。