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作 者:张承彦[1] 谢鑫[2] 张春喜[3] 高登升[4]
机构地区:[1]陕西能源职业技术学院,陕西西安710613 [2]西北大学,陕西西安710069 [3]西安航天总医院麻醉科,陕西西安710100 [4]西安市第四医院新生儿科,陕西西安710014
出 处:《中国病理生理杂志》2013年第8期1441-1446,共6页Chinese Journal of Pathophysiology
摘 要:目的:研究糖蛋白非转移性黑色素瘤蛋白B(glycoprotein nonmetastatic melanoma protein B,GPNMB)对肝癌细胞增殖、凋亡和侵袭能力的影响及其分子机制。方法:以人HepG2细胞为研究对象,构建GPNMB的小干扰RNA(small interfering RNA,siRNA)以及过表达载体,转染入细胞后分别采用MTT法、流式细胞术和Transwell小室法观察其对HepG2细胞增殖、凋亡及侵袭能力的影响。结果:增殖实验结果表明GPNMB可促进HepG2细胞的增殖;流式细胞术检测发现GPNMB对HepG2细胞凋亡几乎无影响;细胞侵袭结果表明GPNMB可促进HepG2细胞的侵袭;当整合素β1亚基基因被siRNA沉默后,GPNMB对HepG2细胞增殖和侵袭的促进作用均受到明显抑制。结论:GPNMB可能通过与整合素β1亚基相互作用促进肝癌细胞的增殖和侵袭能力,提示GPNMB可以作为治疗肝癌的潜在靶点。AIM: To investigate the effect of glycoprotein nonmetastatic melanoma protein B (GPNMB) on the proliferation, apoptosis and invasion of human hepatoma HepG2 cells and its molecular mechanisms. METHODS: The GPNMB siRNA and GPNMB-overexpressing vector were constructed, and then transfected into HepG2 cells. MTT assay, flow cytometry and Transwell chamber were used to determine the effects of GPNMB down-regulation and up-regulation on the proliferation, apoptosis and invasive ability of HepG2 cells. P^SULTS: The proliferation of HepG2 cells was obviously promoted by the up-regulation of GPNMB. No effect of GPNMB on the apoptosis of HepG2 cells was observed. The invasion of HepG2 cells was also significantly promoted by the up-regulation of GPNMB. When integrin β1 was silenced by siRNA, the promoting effect of GPNMB on the proliferation and invasive ability of HepG2 cells was significantly suppressed. CONCLUSION: GPNMB may promote the proliferation and invasion ofHepG2 cells by the interaction with integrin β1, and may be used as a potential therapeutic target in liver cancer. [
关 键 词:糖蛋白非转移性黑色素瘤蛋白B HEPG2细胞 细胞增殖 细胞凋亡 肿瘤侵袭
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