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巨噬细胞帽蛋白与胃癌细胞增殖及迁移能力的关系

[Relationship between macrophage capping protein and gastric cancer cell's proliferation and migration ability].

出版信息

Beijing Da Xue Xue Bao Yi Xue Ban. 2017 Jun 18;49(3):489-494.

Abstract

OBJECTIVE

To investigate the effect of macrophage-capping protein (CapG) on migration and proliferation of human gastric cancer cell line.

METHODS

Real-time PCR method was used to detect the expression of CapG gene in four gastric cancer cell lines, and AGS cells with low expression and transfection were selected as the research objects. Specific primers were designed for CapG and recombinant plasmids synthesized. A lentivirus packaging system which could express CapG was constructed, and a cell line stably expressing CapG was established by infecting human gastric cancer cell line AGS cells. The effect of overexpression of CapG gene on the growth and proliferation of AGS cells was analyzed by CCK8 assay. Cells cratch and Transwell assay were used to analyze the effect of overexpression of CapG gene on AGS cell migration.

RESULTS

After the overexpression of CapG, the growth rate of AGS cells was slightly lower than that of the control group, but there was no significant difference between the two groups (t=2.424, P=0.073). Scratch test showed that the average narrowing distance of the scratches in the CapG experimental group was significantly reduced compared with the control group, the average narrowing distance of the CapG experimental group and the control group was 336.99 μm and 45.54 μm, the difference was statistically significant (t=14.97, P=0.004). The average number of cell penetra-ting membrane in the CapG experimental group and the eGFP control group was 176 and 70, the number of the cells in the CapG experimental group was significantly higher than that of the control group (t=40.00, P<0.001).

CONCLUSION

The overexpression of CapG gene has no significant effect on the growth and proliferation of AGS cells of gastric cancer cell line. Overexpression of CapG gene can promote the migration of AGS cells of gastric cancer cell lines.

摘要

目的

探讨巨噬细胞帽蛋白(CapG)对人胃癌细胞系迁移和增殖的影响。

方法

采用实时荧光定量聚合酶链反应(Real-time PCR)法检测4种胃癌细胞系中CapG基因的表达,选取低表达的AGS细胞进行转染作为研究对象。设计CapG特异性引物并合成重组质粒。构建可表达CapG的慢病毒包装系统,通过感染人胃癌细胞系AGS细胞建立稳定表达CapG的细胞系。采用细胞计数试剂盒(CCK8)法分析CapG基因过表达对AGS细胞生长和增殖的影响。采用细胞划痕实验和Transwell实验分析CapG基因过表达对AGS细胞迁移的影响。

结果

CapG过表达后,AGS细胞的生长速率略低于对照组,但两组间差异无统计学意义(t=2.424,P=0.073)。划痕实验显示,CapG实验组划痕平均缩窄距离较对照组显著减小,CapG实验组和对照组划痕平均缩窄距离分别为336.99μm和45.54μm,差异有统计学意义(t=14.97,P=0.004)。CapG实验组和增强绿色荧光蛋白(eGFP)对照组细胞穿膜平均数分别为176和70,CapG实验组细胞数显著高于对照组(t=40.00,P<0.001)。

结论

CapG基因过表达对胃癌细胞系AGS细胞的生长和增殖无显著影响。CapG基因过表达可促进胃癌细胞系AGS细胞的迁移。

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