CRIM1基因对胃癌细胞增殖和凋亡的影响及其预后价值
吴昆哲, 戴冬秋中国医科大学附属第四医院胃肠外科, 沈阳 110032
收稿日期:
2019-07-11出版日期:
2020-06-30发布日期:
2020-06-15通讯作者:
戴冬秋E-mail:daidq63@163.com作者简介:
吴昆哲(1993-),男,硕士研究生.关键词: 胃癌, 增殖, 凋亡, 富含半胱氨酸型运动神经元蛋白1
Abstract: Objective To investigate the prognostic value of cysteine-rich motor neuron 1 (CRIM1) expression in gastric cancer (GC) and the effects of silencing CRIM1 on the proliferation and apoptosis of GC cells. Methods TCGA and Kaplan-Meier plotter databases were used to analyze CRIM1 expression in GC and its relationship with the prognosis of GC patients. The expression of CRIM1 in AGS cells was reduced by siRNA transfection,and the effect of silencing was verified. MTT assay and flow cytometry were performed to investigate the effects of silencing CRIM1 on the proliferation and apoptosis of AGS cells. Western blotting was used to detect the expression of the apoptosis-related proteins BCL-2 and BAX in AGS cells. Results The results of bioinformatics analysis showed that CRIM1 expression in GC tissues was significantly higher than that in normal gastric tissues and that GC patients with low CRIM1 expression had longer overall survival than those with high CRIM1 expression (P<0.05). The expression of CRIM1 protein in the group of transfected AGS cells was significantly lower than that in the blank control group and the negative control group (P<0.05). In CRIM1-silenced AGC cells relative to control cells,the proliferation rate was decreased,the apoptosis rate was increased,the expression of BCL-2 protein was decreased,and the expression of BAX protein was increased (P<0.05). Conclusion High expression of CRIM1 is associated with poor prognosis of GC patients. Silencing CRIM1 can inhibit the proliferation of AGS cells and induce their apoptosis.
Key words: gastric cancer, proliferation, apoptosis, cysteine-rich motor neuron 1
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