首页> 美国卫生研究院文献>Aging (Albany NY) >RNF168 is highly expressed in esophageal squamous cell carcinoma and contributes to the malignant behaviors in association with the Wnt/β-catenin signaling pathway
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RNF168 is highly expressed in esophageal squamous cell carcinoma and contributes to the malignant behaviors in association with the Wnt/β-catenin signaling pathway

机译:RNF168在食管鳞状细胞癌中高度表达与WNT /β-Catenin信号通路相关联的恶性行为有助于

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摘要

E3 ubiquitin ligase RING finger protein 168 (RNF168) is one of the key proteins in DNA damage repair. Abnormal expression of RNF168 has recently been found in some tumors. However, the role of RNF168 in the development of esophageal squamous cell carcinoma (ESCC) has not been fully elucidated. Here we report that expression of RNF168 in esophageal squamous cell carcinoma is increased with respect to normal esophageal epithelial tissue. Notably, in ESCC patients, increased RNF168 expression was associated with tumor stage and depth of invasion. Knockdown of the RNF168 gene inhibited proliferation of esophageal cancer cells, promoted cell apoptosis, and interfered with cell movement, ultimately inhibiting tumor xenograft growth. Mechanistic studies showed that RNF168 influenced the malignant behavior of esophageal cancer cells by regulating the Wnt/ β-catenin signaling pathway. In addition, RNF168 expression was positively correlated with wingless-type MMTV integration site family member 3A (WNT3A) expression, and high expression of RNF168 and WNT3A predicted a low survival rate. In conclusion, our findings highlight the important role of RNF168 in ESCC tumorigenesis and provide new biomarkers and therapeutic targets for the treatment of ESCC.
机译:E3泛素连接酶环形手指蛋白质168(RNF168)是DNA损伤修复中的关键蛋白之一。在一些肿瘤中发现了RNF168的异常表达。然而,RNF168在食管鳞状细胞癌(ESCC)的发育中的作用尚未完全阐明。在这里,我们认为RNF168在食管鳞状细胞癌中的表达相对于正常食管上皮组织增加。值得注意的是,在ESCC患者中,增加的RNF168表达与肿瘤阶段和入侵深度相关。 RNF168基因的敲低抑制食管癌细胞的增殖,促进细胞凋亡,并干扰细胞运动,最终抑制肿瘤异种移植生长。机械研究表明,RNF168通过调节WNT /β-Catenin信号通路来影响食管癌细胞的恶性行为。另外,RNF168表达与无翼型MMTV集成位点系列构件3A(WNT3A)表达呈正相关,RNF168和WNT3A的高表达预测生存率低。总之,我们的研究结果突出了RNF168在ESCC肿瘤瘤中的重要作用,并为ESCC提供了新的生物标志物和治疗靶标。

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