首页> 美国卫生研究院文献>Molecular Medicine Reports >Resveratrol inhibits the invasion and metastasis of colon cancer through reversal of epithelial- mesenchymal transition via the AKT/GSK-3β/Snail signaling pathway
【2h】

Resveratrol inhibits the invasion and metastasis of colon cancer through reversal of epithelial- mesenchymal transition via the AKT/GSK-3β/Snail signaling pathway

机译:白藜芦醇通过AKT /GSK-3β/ Snail信号通路逆转上皮-间质转化抑制结肠癌的侵袭和转移

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The identification of safe and effective drugs that inhibit tumor invasion and metastasis is required to improve the clinical outcome of patients with colon cancer. The present study aimed to investigate the inhibitory effects and possible mechanisms of action of resveratrol against the invasion and metastasis of colon cancer. AKT1-knockdown SW480 and SW620 colon cancer cells were used to detect the effects of resveratrol on cell invasion and metastasis, as well as changes in the expression of epithelial-mesenchymal transition (EMT) markers and serine/threonine kinase (AKT)/glycogen synthase kinase (GSK)-3β/Snail signaling pathway-related molecules in vitro. Furthermore, nude mice were inoculated with SW480 cells in the tail vein to establish an in vivo lung metastasis model of colon cancer, to investigate the effects of resveratrol on lung metastasis in colon cancer. The results revealed that resveratrol treatment and AKT1 knockdown significantly inhibited cell migration and invasion in colon cancer, and markedly increased E-cadherin expression and decreased that of N-cadherin, phospho (p)-AKT1, p-GSK-3β, and Snail in colon cancer both in vitro and in vivo. Furthermore, the effects of resveratrol were significantly weaker in the AKT1-knockdown cells. In conclusion, resveratrol may suppress the invasion and metastasis of colon cancer through reversal of EMT via the AKT/GSK-3β/Snail signaling pathway. AKT1 may therefore be a key regulator of EMT in colon cancer cells and a potential therapeutic target for this disease.
机译:需要鉴定出抑制肿瘤侵袭和转移的安全有效的药物,以改善结肠癌患者的临床结局。本研究旨在研究白藜芦醇对结肠癌的侵袭和转移的抑制作用和可能的作用机制。 AKT1抑制SW480和SW620结肠癌细胞用于检测白藜芦醇对细胞侵袭和转移的影响,以及上皮-间质转化(EMT)标记和丝氨酸/苏氨酸激酶(AKT)/糖原合酶表达的变化激酶(GSK)-3β/ Snail信号通路相关分子在体外。此外,在裸鼠的尾静脉中接种SW480细胞以建立结肠癌的体内肺转移模型,以研究白藜芦醇对结肠癌的肺转移的影响。结果表明,白藜芦醇处理和AKT1敲低显着抑制结肠癌中的细胞迁移和侵袭,并显着增加E-钙粘蛋白的表达,并降低N-钙粘蛋白,磷酸(p)-AKT1,p-GSK-3β和Snail的表达。结肠癌在体内和体外都有。此外,白藜芦醇在AKT1抑制细胞中的作用明显减弱。总之,白藜芦醇可以通过AKT /GSK-3β/ Snail信号通路逆转EMT抑制结肠癌的侵袭和转移。因此,AKT1可能是结肠癌细胞EMT的关键调节剂,并且是该疾病的潜在治疗靶标。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号