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LASP-1, regulated by miR-203, promotes tumor proliferation and aggressiveness in human non-small cell lung cancer

机译:由miR-203调控的LASP-1促进人非小细胞肺癌的肿瘤增殖和侵袭性

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摘要

The LIM and SH3 protein 1 (LASP-1) has been reported to be associated with tumor development and progression. However, the expression and potential function of LASP-1 in human non-small cell lung cancer (NSCLC) remains undefined. Thus, this study aims to determine the relationship of LASP-1 expression with the progression and prognosis of NSCLC. Expression of LASP-1 was evaluated in NSCLC tissues and cell lines by real-time PCR, immunohistochemistry and Western blot analysis. The relationship between LASP-1 expression and clinicopathological characteristics was analyzed. The effects of LASP-1 on cell proliferation, migration and invasion were investigated in NSCLC cell lines in vitro and in vivo. Luciferase assay was used to determine whether LASP-1 could be regulated by miR-203. We found that LASP-1 was overexpressed in NSCLC and its expression level was closely correlated with tumor size, advanced TNM stage, lymph node metastasis as well as survival time and could be recognized as an independent prognostic factor of patients. LASP-1 could promote proliferation, migration and invasion of NSCLC cells in vitro and in vivo. Moreover, LASP-1 was proved to be a direct target gene for miR-203. Our results suggest that LASP-1, mediated by miR-203, has crucial functions in the proliferation, migration and invasion of NSCLC. (C) 2015 Elsevier Inc. All rights reserved.
机译:LIM和SH3蛋白1(LASP-1)已被报道与肿瘤的发生和发展有关。但是,LASP-1在人非小细胞肺癌(NSCLC)中的表达和潜在功能仍不确定。因此,本研究旨在确定LASP-1表达与NSCLC的进展和预后之间的关系。通过实时PCR,免疫组织化学和蛋白质印迹分析评估了NSCLC组织和细胞系中LASP-1的表达。分析了LASP-1表达与临床病理特征之间的关系。在体外和体内研究了LASP-1对NSCLC细胞系中细胞增殖,迁移和侵袭的影响。使用萤光素酶测定来确定LASP-1是否可以被miR-203调节。我们发现LASP-1在NSCLC中过表达,其表达水平与肿瘤大小,晚期TNM分期,淋巴结转移以及生存时间密切相关,可以被认为是患者的独立预后因素。 LASP-1可在体外和体内促进NSCLC细胞的增殖,迁移和侵袭。此外,LASP-1被证明是miR-203的直接靶基因。我们的结果表明,由miR-203介导的LASP-1在NSCLC的增殖,迁移和侵袭中具有关键功能。 (C)2015 Elsevier Inc.保留所有权利。

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