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基质溶素在MCF-7细胞中的过表达增强了细胞侵袭性和前明胶酶激活。

Matrilysin over-expression in MCF-7 cells enhances cellular invasiveness and pro-gelatinase activation.

作者信息

Wang Fengqiang, Reierstad Scott, Fishman David A

机构信息

Department of Obstetrics and Gynecology, New York University School of Medicine, 550 First Avenue, NB-9N28, New York, NY 10016, USA.

出版信息

Cancer Lett. 2006 May 18;236(2):292-301. doi: 10.1016/j.canlet.2005.05.042. Epub 2005 Jul 12.

Abstract

Matrilysin (MMP-7) is over-expressed in various cancers and is thought to play important roles in tumor invasion and metastasis. However, the function of MMP-7 in breast cancer remains unclear. We therefore examined the expression of the MMP-7 gene in breast cancer (MCF-7) cells and the effect of its over-expression on cellular invasion. We transfected human MMP-7 into MCF-7 cells and selected clones that stably over-expressed the MMP-7 gene. The in vitro invasiveness of MCF-7 cells was quantified by use of the Matrigel invasion assay. Expression of MMP-7 mRNA was analyzed by quantitative RT-PCR. MMP secretion and activation were detected by gelatin zymography. We found that MMP-7-expressing clones had significantly increased invasion (P < 0.001), with increased MMP-7 expression and gelatinase activation as compared to the vector controls. We conclude that MMP-7 over-expression correlates with breast cancer in vitro invasiveness and that MMP-7 may promote invasion by increasing the secretion and activation of proMMP-2 and proMMP-9.

摘要

基质溶素(MMP - 7)在多种癌症中过度表达,被认为在肿瘤侵袭和转移中起重要作用。然而,MMP - 7在乳腺癌中的功能仍不清楚。因此,我们检测了MMP - 7基因在乳腺癌(MCF - 7)细胞中的表达及其过表达对细胞侵袭的影响。我们将人MMP - 7转染到MCF - 7细胞中,并筛选出稳定过表达MMP - 7基因的克隆。通过基质胶侵袭试验定量检测MCF - 7细胞的体外侵袭性。通过定量RT - PCR分析MMP - 7 mRNA的表达。通过明胶酶谱法检测MMP的分泌和激活。我们发现,与载体对照相比,表达MMP - 7的克隆侵袭性显著增加(P < 0.001),且MMP - 7表达和明胶酶激活增加。我们得出结论,MMP - 7过表达与乳腺癌体外侵袭性相关,并且MMP - 7可能通过增加proMMP - 2和proMMP - 9的分泌和激活来促进侵袭。

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