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中华放射肿瘤学杂志
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中华放射肿瘤学杂志  2021, Vol. 30 Issue (4): 403-406    DOI: 10.3760/cma.j.cn113030-20190902-00359
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miR-133b靶向HER-2对结肠癌细胞放射敏感性影响
赵磊1, 王天玉1, 王晓敏2, 刘俊中1, 易善永3
1郑州大学附属郑州中心医院介入科 450000;
2郑州大学附属郑州中心医院放疗科 450000;
3郑州大学附属郑州中心医院肿瘤科 450000
Effect of miR-133b on radiosensitivity of colon cancer SW620 cells by targeting HER-2
Zhao Lei1, Wang Tianyu1, Wang Xiaomin2, Liu Junzhong1, Yi Shanyong3
1Department of Intervention, Zhengzhou Central Hospital Affiliate to Zhengzhou University, Zhengzhou 450000, China;
2Department of Radiation, Zhengzhou Central Hospital Affiliate to Zhengzhou University, Zhengzhou 450000, China;
3Depatment of Oncology, Zhengzhou Central Hospital Affiliate to Zhengzhou University, Zhengzhou 450000, China
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摘要 目的 研究miR-133b对结肠癌细胞(SW620细胞)凋亡及放射敏感性影响并探讨其机制。方法 采用脂质体法转染miR-con组(转染miR-con)、miR-133b组(转染miR-133b mimics)、si-con组(转染si-con)和si-HER-2组(转染si-HER-2) SW620细胞,然后进行0、2、4、6、8 Gy照射。使用qRT-PCR、Western blot、流式细胞术、克隆形成实验和双荧光素酶报告基因实验分别检测各组细胞中miR-133b表达、HER-2蛋白表达、细胞凋亡、细胞存活分数和细胞荧光活性。结果 与照射前相比,照后SW620细胞中miR-133b表达降低(P<0.05),HER-2表达升高(P<0.05)。过表达miR-133b、敲减HER-2均可降低SW620细胞存活分数(P<0.05),促进细胞凋亡(P<0.05)。miR-133b可抑制野生型HER-2细胞荧光活性(P<0.05),且可负向调控HER-2蛋白表达。结论 miR-133b可抑制SW620细胞存活,促进细胞凋亡,增强放射敏感性,其机制可能与靶向HER-2有关。
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赵磊
王天玉
王晓敏
刘俊中
易善永
关键词 miR-133b基因HER-2基因结肠癌细胞系放射敏感性    
AbstractObjective To evaluate the effect of miR-133b on the apoptosis and radiosensitivity of colon cancer cell line (SW620 cells), and to explore its mechanism. Methods SW620 cells were transfected with miR-con (miR-con group), miR-133b mimics (miR-133b group), si-con (si-con group) and si-HER-2(si-HER-2 group) by the liposome method, and then irradiated with 0, 2, 4, 6, 8 Gy. The miR-133b protein expression, HER-2 protein expression, apoptosis, cell survival fraction and cytofluoroactivity in each group were evaluated by qRT-PCR, Western blot, flow cytometry, colony formation assay and dual luciferase reporter gene assay, respectively. Results Compared with the pre-irradiation group, the expression level of miR-133b was significantly down-regulated (P<0.05), whereas that of HER-2 was significantly up-regulated in SW620 cells after irradiation (P<0.05). Overexpression of miR-133b and knockdown of HER-2 remarkably reduced the survival fraction (both P<0.05),and significantly promoted the apoptosis of SW620 cells (P<0.05). miR-133b could considerably inhibit the fluorescent activity of wild-type HER-2 cells (P<0.05) and negatively regulate the expression of HER-2 protein. Conclusion miR-133b can inhibit the survival of colon cancer cells, promote the apoptosis and enhance the sensitivity of radiotherapy probably via the mechanism of targeting HER-2.
Key wordsmiR-133b gene    HER-2 gene    Colon cancer cell line    Radiosensitivity   
收稿日期: 2019-09-02     
基金资助:河南省医学科技攻关计划省部共建项目(201601030)
通讯作者: 易善永,Email:ranhai186@sina.com   
引用本文:   
赵磊,王天玉,王晓敏等. miR-133b靶向HER-2对结肠癌细胞放射敏感性影响[J]. 中华放射肿瘤学杂志, 2021, 30(4): 403-406.
Zhao Lei,Wang Tianyu,Wang Xiaomin et al. Effect of miR-133b on radiosensitivity of colon cancer SW620 cells by targeting HER-2[J]. Chinese Journal of Radiation Oncology, 2021, 30(4): 403-406.
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