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37-kDa laminin receptor precursor promotes lung adenocarcinoma cell invasion and metastasis by epithelial-to-mesenchymal transition

机译:37 kDa层粘连蛋白受体前体通过上皮向间充质转化促进肺腺癌细胞的侵袭和转移

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37-kDa laminin receptor precursor (37LRP) has a crucial role in migration of some human cancers. Epithelial-to-mesenchymal transition (EMT) has received much attention in invasion and metastasis of lung cancer. Nevertheless, the role of 37LRP is not entirely clear in EMT promotion of lung cancer at present. In this study, we firstly examined the possible role of 37LRP in the invasiveness and metastasis process of lung cancer using immunohistochemistry of 80 lung adenocarcinoma cases, western blot and real-time PCR of 12 fresh lung adenocarcinoma tissues. The results showed that 37LRP significantly correlated with clinical stage and were highly expressed in metastatic lung adenocarcinomas compared with nonmetastatic ones. In vitro, we observed that 37LRP significantly increased the adhesive, invasive and metastatic abilities of human lung adenocarcinoma cell lines A549 by 37LRP-lentivirus interference. Furthermore, inoculation of A549 cells transduced with 37LRP-lentivirus in nude mice resulted in multi-metastases including the lung. In addition, western blotting and immunofluorescence were used to detect the significant difference in expression of E-cadherin and fibronectin in A549 by 37LRP-lentivirus interference compared with 37LRP-small interference RNA-lentivirus interference in vitro and vivo. The data indicated that A549 cells of epithelial cell characteristics might be induced to undergo EMT by 37LRP. A549 cells transduced with 37LRP-lentivirus showed marked morphological changes, accompanied by the decrease of epithelial marker E-cadherin and the increase of mesenchymal marker fibronectin. These results indicated that 37LRP may promote lung adenocarcinoma invasion and metastasis via the mechanism of EMT.
机译:37 kDa层粘连蛋白受体前体(37LRP)在某些人类癌症的迁移中起关键作用。上皮-间质转化(EMT)在肺癌的侵袭和转移中受到了广泛的关注。然而,目前,37LRP在EMT促进肺癌中的作用尚不完全清楚。在这项研究中,我们首先使用80例肺腺癌的免疫组织化学,Western印迹和实时PCR检测12例新鲜肺腺癌组织,研究了37LRP在肺癌的侵袭和转移过程中的可能作用。结果表明,与非转移性肺腺癌相比,37LRP与临床分期显着相关,并在转移性肺腺癌中高表达。在体外,我们观察到37LRP通过37LRP-慢病毒的干扰显着增加了人肺腺癌细胞系A549的粘附,侵袭和转移能力。此外,在裸鼠中接种经37LRP-慢病毒转导的A549细胞会导致包括肺在内的多种转移。此外,采用Western blotting和免疫荧光法检测37LRP-小病毒干扰物与37LRP-小干扰RNA-小病毒干扰物在体外和体内相比,A549中E-钙粘蛋白和纤连蛋白表达的显着差异。数据表明上皮细胞特性的A549细胞可能被37LRP诱导进行EMT。转染37LRP-慢病毒的A549细胞表现出明显的形态学变化,伴随着上皮标志物E-钙黏着蛋白的减少和间充质标志物纤连蛋白的增加。这些结果表明37LRP可能通过EMT机制促进肺腺癌的侵袭和转移。

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