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敲低核糖体蛋白S15A可通过在体外诱导细胞凋亡来抑制乳腺癌细胞的增殖。

Knockdown of ribosomal protein S15A inhibits proliferation of breast cancer cells through induction of apoptosis in vitro.

作者信息

Feng Weiliang, Liang Chenlu, Wang Chen, Yu Xingfei, Li Qinglin, Yang Hongjian

机构信息

Department of Breast Surgery, Zhejiang Cancer Hospital, No. 1 East Banshan Road, Hangzhou, 310022, China.

Zhejiang Chinese Medical University, No. 548 Binwen Road, Hangzhou, 310053, China.

出版信息

Cytotechnology. 2018 Oct;70(5):1315-1323. doi: 10.1007/s10616-018-0221-9. Epub 2018 May 25.

DOI:10.1007/s10616-018-0221-9
PMID:29802490
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6214850/
Abstract

To explore the role of ribosomal protein S15A (RPS15A) in breast cancer. The Oncomine database was used to compare the expression of RPS15A in human breast cancer tissues and normal tissues. RPS15A in breast cancer cell line ZR-75-30 and BT474 was specifically knocked down using lentivirus-mediated short hairpin RNAs (shRNAs). RPS15A knockdown efficiency was validated by quantitative polymerase chain reaction and western blot analysis. Subsequently, the functional effects of RPS15A on proliferation of breast cancer cells were investigated by MTT, colony formation and flow cytometry assays. Functional analysis indicated that RPS15A knockdown could inhibit cell proliferation, induced cell cycle arrest and apoptosis. Mechanism analysis revealed RPS15A mediated apoptosis via activating of caspase-3 and PARP cleavage, upregulating of Bad and BAX and downregulating of Bcl-2. Our preliminary study highlighted the importance of RPS15A in breast cancer growth. The inhibition of RPS15A may be a promising therapeutic target for breast cancer treatment.

摘要

探讨核糖体蛋白S15A(RPS15A)在乳腺癌中的作用。利用Oncomine数据库比较RPS15A在人乳腺癌组织和正常组织中的表达。使用慢病毒介导的短发夹RNA(shRNAs)特异性敲低乳腺癌细胞系ZR-75-30和BT474中的RPS15A。通过定量聚合酶链反应和蛋白质印迹分析验证RPS15A的敲低效率。随后,通过MTT、集落形成和流式细胞术分析研究RPS15A对乳腺癌细胞增殖的功能影响。功能分析表明,敲低RPS15A可抑制细胞增殖,诱导细胞周期停滞和凋亡。机制分析显示,RPS15A通过激活半胱天冬酶-3和PARP裂解、上调Bad和BAX以及下调Bcl-2介导细胞凋亡。我们的初步研究突出了RPS15A在乳腺癌生长中的重要性。抑制RPS15A可能是乳腺癌治疗的一个有前景的治疗靶点。

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本文引用的文献

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Gene. 2014 Feb 15;536(1):84-9. doi: 10.1016/j.gene.2013.11.075. Epub 2013 Dec 12.