首页> 外文期刊>Acta Biochimica et Biophysica Sinica >Nuclear Factor-κB Signaling Pathway Constitutively Activated in Esophageal Squamous Cell Carcinoma Cell Lines and Inhibition of Growth of Cells by Small Interfering RNA
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Nuclear Factor-κB Signaling Pathway Constitutively Activated in Esophageal Squamous Cell Carcinoma Cell Lines and Inhibition of Growth of Cells by Small Interfering RNA

机译:食管鳞癌细胞系中组成性激活的核因子-κB信号通路和小干扰RNA抑制细胞的生长。

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Although constitutive nuclear factor (NF)-κB activation has been reported in many human tumors, the role of the NF-κB pathway in esophageal squamous cell carcinoma (ESCC) has not been known. In this study, NF-κB pathway in two ESCC cell lines was investigated using immunocytochemistry, Western blot and reverse transcrition-polymerase chain reaction. The activation of NF-κB DNA binding was determined by electrophoretic mobility-shift assay. RNA interference was used to specifically inhibit the expression of p65. Growth of cells was evaluated by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay. The results showed that p50, p65, IκBα, p-IκBα and IκB kinase β were expressed and mainly localized in the cytoplasm. Reverse transcription-polymerase chain reaction results showed the constitutive expressions of p50, p65 and IκBα mRNA in the two ESCC cell lines. Furthermore, the nuclear extracts revealed that p50 and p65 translocated to the nucleus had DNA-binding activity. Finally, small interfering RNA of p65 decreased the expression of p65, and the viability of cells transfected with p65 small interfering RNA was significantly suppressed at the same concentration of 5-fluorouracil (P < 0.05) compared to untransfected cells. The results of this study showed that there was the constitutively activated NF-κB signaling pathway in the ESCC cell lines. RNA interference targeting at p65 increased the sensitivity of the ESCC cell lines to 5-fluorouracil, suggesting that NF-κB might be a good target for cancer treatment.
机译:尽管在许多人类肿瘤中已经报道了本构性核因子(NF)-κB的激活,但尚不知道NF-κB途径在食管鳞状细胞癌(ESCC)中的作用。在这项研究中,使用免疫细胞化学,蛋白质印迹和逆转录聚合酶链反应研究了两种ESCC细胞系中的NF-κB途径。 NF-κBDNA结合的激活是通过电泳迁移率变动分析确定的。 RNA干扰被用于特异性抑制p65的表达。细胞生长通过3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴化物测定来评估。结果显示p50,p65,IκBα,p-IκBα和IκB激酶β表达且主要定位于细胞质中。逆转录-聚合酶链反应结果显示在两种ESCC细胞系中p50,p65和IκBαmRNA的组成型表达。此外,核提取物显示p50和p65易位至细胞核具有DNA结合活性。最后,与相同浓度的5-氟尿嘧啶相比,p65小干扰RNA降低了p65的表达,并且在相同浓度的5-氟尿嘧啶下,p65小干扰RNA转染的细胞的活力被显着抑制(P <0.05)。这项研究的结果表明,ESCC细胞系中存在组成性激活的NF-κB信号通路。靶向p65的RNA干扰增加了ESCC细胞系对5-氟尿嘧啶的敏感性,这表明NF-κB可能是治疗癌症的好靶标。

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