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OCT4B1的抑制促进了肿瘤细胞系中抗凋亡基因的下调。

Down-regulation of anti-apoptotic genes in tumor cell lines is facilitated by suppression of OCT4B1.

作者信息

Mirzaei Mohammad Reza, Mahmoodi Mehdi, Hassanshahi Gholamhossein, Ahmadi Zahra

机构信息

Molecular Medicine Research Center, Rafsanjan University of Medical Sciences, Rafsanjan, Iran.

Molecular Medicine Research Center, Rafsanjan University of Medical Sciences, Rafsanjan, Iran.

出版信息

Adv Med Sci. 2017 Mar;62(1):97-102. doi: 10.1016/j.advms.2016.04.004. Epub 2016 May 10.

Abstract

PURPOSE

The OCT4B1 as a variant of OCT4 is expressed in both cancer cells and tissues. The anti-apoptotic property of this variant aid cancer cells to escape from apoptosis. Therefore, the aim of the present study was to determine the effects of OCT4B1 suppression on regulation of 25 genes involved in anti-apoptotic pathway in tumor cell lines.

MATERIAL AND METHODS

AGS (gastric adenocarcinoma), 5637 (bladder tumor) and U-87MG (brain tumor) cells were transfected with specific OCT4B1 siRNA and a scramble siRNA by siRNA silencing gene technology, using Lipofectamine 2000 commercial kit. The real-time PCR technique was employed to examine and calculate fold changes of evaluated genes using the 2 formula.

RESULTS

Present results demonstrated that 22 (88%) of interested genes were similarly down-regulated in all three examined cell lines. Our results also indicated that three genes (CASP2, IGF1R,TNF) were up-regulated. The CFLAR gene was down-regulated in AGS, while it was inversely up-regulated in 5637 and U87MG cells.

CONCLUSIONS

It may possibly be concluded that suppression of OCT4B1 can lead to apoptosis in tumor cell lines and this is at least facilitated via down-regulation of examined anti-apoptotic genes. Accordingly, suppression of OCT4B1 may probably be considered as useful tool in cancer therapy and research.

摘要

目的

OCT4B1作为OCT4的一种变体,在癌细胞和组织中均有表达。该变体的抗凋亡特性有助于癌细胞逃避凋亡。因此,本研究的目的是确定抑制OCT4B1对肿瘤细胞系中25个参与抗凋亡途径的基因调控的影响。

材料与方法

采用Lipofectamine 2000商业试剂盒,通过小干扰RNA(siRNA)沉默基因技术,将特异性OCT4B1 siRNA和乱序siRNA转染至AGS(胃腺癌)、5637(膀胱肿瘤)和U-87MG(脑肿瘤)细胞。采用实时聚合酶链反应(PCR)技术,使用2公式检测并计算评估基因的倍数变化。

结果

目前的结果表明,在所有三种检测的细胞系中,22个(88%)感兴趣的基因均被类似地下调。我们的结果还表明,三个基因(CASP2、IGF1R、TNF)被上调。CFLAR基因在AGS细胞中被下调,而在5637和U87MG细胞中则呈相反的上调。

结论

可以得出结论,抑制OCT4B1可导致肿瘤细胞系凋亡,这至少是通过下调检测的抗凋亡基因来实现的。因此,抑制OCT4B1可能被认为是癌症治疗和研究中的一种有用工具。

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