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HER2/neu原癌基因对尿激酶型纤溶酶原激活剂表达的上调作用。

Up-regulation of urokinase-type plasminogen activator expression by the HER2/neu proto-oncogene.

作者信息

Gum R, Wang S W, Lengyel E, Yu D, Hung M C, Juarez J, Boyd D

机构信息

Department of Tumor Biology, M. D. Anderson Cancer Center, Houston, Texas 77030, USA.

出版信息

Anticancer Res. 1995 Jul-Aug;15(4):1167-72.

PMID:7653995
Abstract

The HER2/neu (c-erbB2) protooncogene, which encodes a transmembrane receptor (p185neu), contributes to tumor cell invasion/metastasis through mechanism(s) which are, at present, poorly defined. Since basement membrane degradation is a prerequisite for tumor progression, we undertook a study to determine if the expression of urokinase, a key protease implicated in extracellular matrix proteolysis, was regulated by this oncogene. Stable overexpression of a cDNA encoding HER2/neu in H460 lung cancer cells led to elevated secretion of urokinase which was a consequence of a higher level of protease mRNA. Transfection of the HER2/neu-overexpressing B 104-1 cells with a CAT reporter construct driven by the urokinase promoter, gave rise to increased CAT activity when compared with parental NIH3T3 cells, which have low levels of HER2/neu, suggesting that the protooncogene can enhance urokinase promoter activity. Since the enhanced expression of HER2/neu results in increased tumor invasion/metastasis (1), these data suggest that, at least in vitro, HER2/neu-induced expression of urokinase may contribute to tumor progression in p185neu-positive cancers.

摘要

HER2/neu(c-erbB2)原癌基因编码一种跨膜受体(p185neu),其通过目前尚不清楚的机制促进肿瘤细胞的侵袭/转移。由于基底膜降解是肿瘤进展的前提条件,我们开展了一项研究,以确定尿激酶(一种参与细胞外基质蛋白水解的关键蛋白酶)的表达是否受该原癌基因调控。在H460肺癌细胞中稳定过表达编码HER2/neu的cDNA导致尿激酶分泌增加,这是蛋白酶mRNA水平升高的结果。用尿激酶启动子驱动的CAT报告基因构建体转染过表达HER2/neu的B104-1细胞,与HER2/neu水平较低的亲代NIH3T3细胞相比,CAT活性增加,这表明该原癌基因可增强尿激酶启动子活性。由于HER2/neu的过表达导致肿瘤侵袭/转移增加(1),这些数据表明,至少在体外,HER2/neu诱导的尿激酶表达可能有助于p185neu阳性癌症的肿瘤进展。

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