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ALDH3A1 acts as a prognostic biomarker and inhibits the epithelial mesenchymal transition of oral squamous cell carcinoma through IL-6/STAT3 signaling pathway

机译:Aldh3a1作为预后生物标志物,通过IL-6 / Stat3信号通路抑制口腔鳞状细胞癌的上皮间充质转变

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Objectives: Aldehyde dehydrogenase 3A1 (ALDH3A1) is a member of the ALDH superfamily and its relationship with oral squamous cell carcinoma (OSCC) still unknown. In our subject, we aimed to reveal the expression pattern and clinical value of ALDH3A1 in OSCC and its biological function in OSCC cell lines. Materials and methods: The expression level of ALDH3A1 in paired OSCC tissues and adjacent noncancerous tissues were detected by quantitative real-time PCR, Western blot and immunohistochemistry. The relationship between ALDH3A1 expression and clinical characteristics was analyzed. Besides, cell-counting kit 8, colony formation, wound healing, transwell invasion, apoptosis and cell cycle assays were employed to assess the role of ALDH3A1 in OSCC cells. To explore the influence of ALDH3A1 on OSCC epithelial-to-mesenchymal transition (EMT), the expression of EMT markers (E-cadherin, vimentin, snail, MMP3) on OSCC cells were detected, and possible mechanisms were analyzed. Results: In OSCC tissues, ALDH3A1 was significantly decreased compared to the adjacent normal tissues. Lower ALDH3A1 expression in OSCC tissues was associated with a higher incidence of lymph node metastasis (LNM). Moreover, the overall survival of OSCC with low ALDH3A1 expression was significantly worse compared to that of OSCC with high ALDH3A1 expression. Restored expression of ALDH3A1 suppressed cell proliferation, migration and invasion in OSCC cells. Further experiments showed that ALDH3A1 might inhibit EMT in OSCC via a regulation of the IL-6/STAT3 signal pathway. Conclusion: These data indicate that ALDH3A1 may serve as a biomarker and may be developed into a novel treatment for OSCC.? The author(s).
机译:目的:醛脱氢酶3a1(Aldh3a1)是Aldh超家族的成员及其与口腔鳞状细胞癌(OSCC)的关系仍然未知。在我们的主题中,我们旨在揭示ALDH3A1在OSCC中的表达模式和临床价值及其在OSCC细胞系中的生物学功能。材料和方法:通过定量的实时PCR,Western印迹和免疫组化检测成对OSCC组织和相邻的非癌组织中AldH3a1的表达水平。分析了ALDH3A1表达与临床特征之间的关系。此外,使用细胞计数试剂盒8,菌落形成,伤口愈合,Transwell侵袭,细胞凋亡和细胞周期测定以评估Aldh3A1在OSCC细胞中的作用。为了探讨AldH3a1对OSCC上皮 - 间充质转换(EMT)的影响,检测到OSCC细胞对OSCC细胞的EMT标记(E-Cadherin,Vimentin,蜗牛,MMP3)的表达,并分析了可能的机制。结果:与邻近的正常组织相比,在OSCC组织中,AldH3a1显着降低。 OSCC组织中的降低AldH3A1表达与淋巴结转移(LNM)的发病率较高。此外,与具有高AldH3A1表达的OSCC相比,具有低AldH3A1表达的OSCC的整体存活率显着差。恢复Aldh3a1的表达抑制细胞增殖,迁移和侵袭在OSCC细胞中。进一步的实验表明,ALDH3A1可以通过IL-6 / Stat3信号途径的调节抑制OSCC的EMT。结论:这些数据表明ALDH3A1可以用作生物标志物,并且可以开发成用于OSCC的新型处理。作者。

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