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首页> 外文期刊>International Journal of Molecular Sciences >TNF-α Gene Knockout in Triple Negative Breast Cancer Cell Line Induces Apoptosis
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TNF-α Gene Knockout in Triple Negative Breast Cancer Cell Line Induces Apoptosis

机译:三阴性乳腺癌细胞系中的TNF-α基因敲除诱导凋亡。

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Tumor necrosis factor alpha (TNF-α) is a pro-inflammatory cytokine involved in the promotion and progression of cancer, including triple negative breast cancer cells. Thus, there is significant interest in understanding the molecular signaling pathways that connect TNF-α with the survival of tumor cells. In our experiments, we used as an in vitro model for triple negative breast cancer the cell line Hs578T. The purpose of this study is to determine the gene expression profiling of apoptotic signaling networks after blocking TNF-α formation by using specially designed siRNA molecules to target TNF-α messenger RNA. Knockdown of TNF-α gene was associated with cell proliferation inhibition and apoptosis, as observed by monitoring the cell index using the xCELLigence RTCA System and flow cytometry. PCR array technology was used to examine the transcript levels of 84 genes involved in apoptosis. 15 genes were found to be relevant after comparing the treated group with the untreated one of which 3 were down-regulated and 12 up-regulated. The down-regulated genes are all involved in cell survival, whereas the up-regulated ones are involved in and interact with pro-apoptotic pathways. The results described here indicate that the direct target of TNF-α in the Hs578T breast cancer cell line increases the level of certain pro-apoptotic factors that modulate different cellular networks that direct the cells towards death.
机译:肿瘤坏死因子α(TNF-α)是一种促炎细胞因子,参与包括三阴性乳腺癌细胞在内的癌症的促进和发展。因此,对理解将TNF-α与肿瘤细胞的存活联系起来的分子信号传导途径有着极大的兴趣。在我们的实验中,我们将Hs578T细胞系用作三阴性乳腺癌的体外模型。这项研究的目的是通过使用专门设计的siRNA分子靶向TNF-α信使RNA来确定阻断TNF-α形成后凋亡信号网络的基因表达谱。通过使用xCELLigence RTCA系统和流式细胞仪监测细胞指数可以观察到,TNF-α基因的抑制与细胞增殖抑制和凋亡相关。 PCR阵列技术用于检查涉及凋亡的84个基因的转录水平。将治疗组与未治疗组进行比较后,发现15个基因是相关的,其中3个被下调,而12个被上调。下调的基因都参与细胞存活,而上调的基因则参与促凋亡途径并与之相互作用。此处描述的结果表明,Hs578T乳腺癌细胞系中TNF-α的直接靶点增加了某些促凋亡因子的水平,这些促凋亡因子调节着指导细胞死亡的不同细胞网络。

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