Zhang Yi, Song Xilin, Gong Weipeng, Zhu Zhenyu, Liu Xin, Hou Qingsheng, Sun Yanlai, Chai Jie, Zou Lei, Guan Jie
Department of Gastrointestinal Surgery, Shandong Tumor Hospital, Jinan, 250017, China.
Cell Biochem Biophys. 2015 Mar;71(2):579-85. doi: 10.1007/s12013-014-0237-5.
RLIP76, a multidomain protein which is a downstream effector of the small GTP ases RalA and RalB, is known to play a role in biological activities in a variety of malignant cancer cells. However, little study has been done on the role of RLIP76 in CRC. In this study, a RLIP76-targeted siRNA-containing vector was used to investigate the effect of RLIP76 knockdown on cellular functions in human CRC cell line HT29. Quantitative RT-PCR and Western blot analysis revealed that the expression levels of RLIP76 mRNA and protein in HT29 cells were significantly suppressed after transfection. Our results indicated that RLIP76 downregulation in HT29 CRC cells suppressed cell growth, enhanced cell apoptosis, induced cell cycle arrest, and inhibited cell invasion by decreasing MMP2 expression. Although the mechanisms through which RLIP76 regulates the cellular functions needs further investigation, our results indicate that RLIP76 may represent as a potential target of gene therapy for CRC treatment.
RLIP76是一种多结构域蛋白,是小GTP酶RalA和RalB的下游效应器,已知其在多种恶性癌细胞的生物学活性中发挥作用。然而,关于RLIP76在结直肠癌(CRC)中的作用研究甚少。在本研究中,使用含RLIP76靶向小干扰RNA(siRNA)的载体来研究RLIP76敲低对人CRC细胞系HT29细胞功能的影响。定量逆转录聚合酶链反应(RT-PCR)和蛋白质免疫印迹分析显示,转染后HT29细胞中RLIP76 mRNA和蛋白质的表达水平显著受到抑制。我们的结果表明,HT29 CRC细胞中RLIP76表达下调会抑制细胞生长、增强细胞凋亡、诱导细胞周期停滞,并通过降低基质金属蛋白酶2(MMP2)的表达来抑制细胞侵袭。尽管RLIP76调节细胞功能的机制需要进一步研究,但我们的结果表明,RLIP76可能是CRC治疗基因疗法的一个潜在靶点。