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LncRNA PVT1在结直肠癌细胞增殖、侵袭和转移中的作用

Role of LncRNA PVT1 in proliferation,invasion and metastasis of colorectal cancer cells
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摘要 目的探讨长链非编码RNAs(lncRNAs)浆细胞瘤多样异位基因1(PVT1)在结直肠癌细胞增殖、侵袭和转移中的作用。方法结直肠癌细胞株HT-29分为三组,干扰PVT1(si-PVT1)组转染si-PVT1,干扰对照(si-NC)组转染si-NC,空白组不进行转染。采用CCK-8法检测24h、48h细胞增殖,流式细胞术检测细胞凋亡,划痕实验检测细胞迁移,Transwell小室检测细胞侵袭。结果转染后24h、48h,与空白组和si-NC组相比,si-PVT1组的LncRNAPVT1表达量显著减少(P<0.05),细胞增殖抑制率显著降低(P<0.05),细胞凋亡率显著降低(P<0.05),细胞划痕愈合率、细胞侵袭率都显著增加(P<0.05)。结论LncRNAPVT1在结直肠癌中可发挥抑癌基因的作用,抑制LncRNAPVT1的表达从而促进结直肠癌细胞增殖、侵袭和转移,抑制细胞凋亡。 Objective To investigate the role of long-chain non-coding RNAs (LncRNA plasmacytoma variant translocation (PVT1) in the proliferation,invasion and metastasis of colorectal cancer cells. Methods Colorectal cancer cell line HT-29 was divided into three groups. Si-PVT1 group was transfected with si-PVT1,si-NC group was transfected with si-NC,and blank group was not transfected. Cell proliferation was detected by CCK-8 method,apoptosis were detected by flow cytometry,cell migration were detected by scratch test,and cell invasion were detected by Transwell chamber. Results At 24 h and 48 h after transfection,the expression of LncRNA PVT1 were significantly decreased in the si-PVT1 group compared with the si-NC group ( P <0.05),and the cell proliferation inhibition rates were significantly decreased ( P <0.05). The apoptotic rates were significantly decreased ( P <0.05),and the cell scratch healing rate and cell invasion rate were significantly increased ( P <0.05). Conclusion LncRNA PVT1 can play a role as a tumor suppressor gene in colorectal cancer. Inhibition of LncRNA PVT1 expression can promote the proliferation,invasion and metastasis of colorectal cancer cells and inhibit cell apoptosis.
作者 姜帅 杨丽丽 杨威 JIANG Shuai;YANG Li-li;YANG Wei(Department of Colorectal,Xi'an Hospital of TCM,Xi'an Shaanxi 710069,China)
出处 《临床和实验医学杂志》 2019年第13期1384-1386,共3页 Journal of Clinical and Experimental Medicine
基金 陕西省科学技术研究发展计划项目(编号:2013k12-07-06)
关键词 结直肠癌 长链非编码RNAs 浆细胞瘤多样异位基因1 细胞侵袭 细胞转移 Colorectal cancer Long-chain non-coding RNAs Plasma cell tumor diverse ectopic gene 1 Cell invasion Cell transfer
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