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首页> 外文期刊>Oncology letters >Role of miR-214 in modulating proliferation and invasion of human colon cancer SW620 cells
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Role of miR-214 in modulating proliferation and invasion of human colon cancer SW620 cells

机译:miR-214在调节人结肠癌SW620细胞的增殖和侵袭中的作用

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This study investigated the role of miR-214 in modulating proliferation and invasion of human colon cancer SW620 cells. Fifty-five patients with colon cancer who were treated in China-Japan Union Hospital of Jilin University from March 2014 to March 2015 were enrolled into this study. Their cancer and corresponding paracancerous tissues were collected and the expression levels of miR-214 were determined by RT-qPCR. A miR-214 expression vector was constructed. SW620 cells were transfected with the miR-214 expression vector and a blank vector. Cells transfected with the miR-214 expression vector were assigned to the miR-214 positive group and cells transfected with the blank vector were assigned to the miR-214 negative group. Cell proliferation, invasion and apoptosis were assessed by MTT assay, Transwell migration assay and TUNEL apoptosis assay, respectively. The RT-qPCR results showed that the expression level of miR-214 in colon cancer tissue, as well as in miR-214 negative cells, was significantly lower than that in paracancerous tissue (P0.05 for both). In cell comparison, the expression level of miR-214 in the miR-214 positive group was significantly higher than that in the miR-214 negative group (0.483 +/- 0.001 vs. 0.172 +/- 0.001; P0.05). The proliferation level of SW620 cells in the miR-214 positive group was lower than that in the miR-214 negative group (P0.05). The Transwell migration assay indicated that there were less cells penetrating the membrane in the miR-214 positive group than in the miR-214 negative group (P0.05). In addition, The apoptosis rate of cells in the miR-214 negative group was significantly lower than that in the miR-214 positive group (P0.05). Finally, the low expression of miR-214 was found in colon cancer, indicating that miR-214 is a cancer suppressor playing an opposing role in colon cancer onset and progression. Therefore, miR-214 can promote apoptosis of colon cancer cells SW620 by inhibiting their proliferation and invasion.
机译:本研究研究了MIR-214在调节人结肠癌SW620细胞的增殖和侵袭方面的作用。从2014年3月到2015年3月,在2015年3月至2015年3月,吉林大学中日本联盟医院治疗的五十五名患有结肠癌的患者入学。收集其癌症和相应的副癌组织,并通过RT-QPCR测定miR-214的表达水平。构建了miR-214表达载体。用miR-214表达载体和空白载体转染SW620细胞。将用miR-214表达载体转染的细胞分配给miR-214阳性基团,并将用空白载体转染的细胞分配给miR-214阴性组。通过MTT测定,Transwell迁移测定和Turnel凋亡测定分别评估细胞增殖,侵袭和细胞凋亡。 RT-QPCR结果表明,结肠癌组织中miR-214的表达水平,以及MiR-214阴性细胞,显着低于副血管组织中的癌症组织(P <0.05)。在细胞比较中,miR-214阳性组中miR-214的表达水平显着高于MiR-214阴性组(0.483 +/- 0.001,0.172 +/- 0.001; p <0.05)。 MIR-214阳性基团SW620细胞的增殖水平低于MiR-214阴性基团的细胞(P <0.05)。 Transwell迁移测定表明,在MiR-214正组中渗透膜的细胞较少,而不是MiR-214阴性组(P <0.05)。此外,MiR-214阴性组细胞的凋亡率显着低于MiR-214阳性基团(P <0.05)。最后,在结肠癌中发现miR-214的低表达,表明miR-214是在结肠癌发作和进展中发挥对立作用的癌症抑制。因此,MIR-214通过抑制其增殖和侵袭来促进结肠癌细胞SW620的凋亡。

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