Suppr超能文献

通过小干扰RNA阻断RLIP76可抑制HT29结肠癌细胞的增殖,增强其凋亡,并抑制其侵袭。

RLIP76 blockade by siRNA inhibits proliferation, enhances apoptosis, and suppresses invasion in HT29 colon cancer cells.

作者信息

Zhang Yi, Song Xilin, Gong Weipeng, Zhu Zhenyu, Liu Xin, Hou Qingsheng, Sun Yanlai, Chai Jie, Zou Lei, Guan Jie

机构信息

Department of Gastrointestinal Surgery, Shandong Tumor Hospital, Jinan, 250017, China.

出版信息

Cell Biochem Biophys. 2015 Mar;71(2):579-85. doi: 10.1007/s12013-014-0237-5.

Abstract

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.

摘要

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。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验