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Serum response factor is overexpressed in esophageal squamous cell carcinoma and promotes Eca-109 cell proliferation and invasion

机译:血清反应因子在食管鳞状细胞癌中过表达,并促进Eca-109细胞增殖和侵袭

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摘要

Recent studies indicate that serum response factor (SRF) is highly expressed in tumors such as hepatocellular, thyroid, esophageal and lung carcinoma. However, the expression and roles of SRF in esophageal squamous cell carcinoma (ESCC) are unclear. In this study, immunohistochemistry was used to compare the expression of SRF in ESCC cases (n=73) and normal controls (n=30). The RNA interference (RNAi) technique was used to knock down the expression of SRF in Eca-109 cells. Cell proliferation, cell cycle stage and invasion were measured with cell counting kit (CCK)-8, flow cytometry and Transwell assays, respectively. Western blotting was used to measure SRF, E-cadherin, beta-catenin and cyclin D1 expression in Eca-109 cells treated with siRNA. The study demonstrated that human ESCC has increased expression of SRF. In addition, blocking SRF expression inhibited tumor proliferation and invasion. In conclusion, SRF has the potential to be a new marker for ESCC diagnosis and therapy.
机译:最近的研究表明,血清反应因子(SRF)在诸如肝细胞癌,甲状腺癌,食道癌和肺癌等肿瘤中高表达。但是,尚不清楚SRF在食管鳞状细胞癌(ESCC)中的表达和作用。在这项研究中,使用免疫组织化学比较了SCC在ESCC病例(n = 73)和正常对照(n = 30)中的表达。 RNA干扰(RNAi)技术被用于敲除Eca-109细胞中SRF的表达。用细胞计数试剂盒(CCK)-8,流式细胞术和Transwell测定法分别测量细胞增殖,细胞周期阶段和侵袭。 Western印迹法用于测量经siRNA处理的Eca-109细胞中SRF,E-钙粘着蛋白,β-连环蛋白和细胞周期蛋白D1的表达。该研究表明,人类ESCC增加了SRF的表达。另外,阻断SRF表达抑制了肿瘤的增殖和侵袭。总之,SRF有可能成为ESCC诊断和治疗的新标志。

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