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主要基质金属蛋白酶在浸润性乳腺癌不同局部区域的表达增强及激活

Enhanced expression and activation of major matrix metalloproteinases in distinct topographic areas of invasive breast carcinomas.

作者信息

Bachmeier Beatrice E, Rohrbach Helmut, De Waal Johann, Jochum Marianne, Nerlich Andreas G

机构信息

Department of Clinical Chemistry and Clinical Biochemistry, Ludwig-Maximilians-University, Germany.

出版信息

Int J Oncol. 2005 May;26(5):1203-7.

Abstract

Matrix metalloproteinases (MMPs) play a key role in events related to tumor cell invasion and growth. Therefore, we examined tumor tissue samples from 12 individuals with invasive breast cancer for the expression and localization of MMP-1, -2, -3 and -9. These were detected by immunohistochemistry. Simultaneously in this material the matrix-degrading enzyme activity was tested by in situ zymography. Additionally, we used a spheroid model of two breast cancer cell lines (MCF-7 and MDA-MB-435) for MMP-expression and activity by immunohistochemistry and in situ zymography. Semi-quantitative investigation of various MMPs by immunohistochemistry in tissue samples revealed higher expression levels at the tumor periphery where tumor cells grow less compact when compared to compact tumor cell complexes as in the center of the tumors. In situ gelatinolytic activity paralleled these observations showing pronounced activity at the tumor periphery when compared to tumor centers. Similarly, tumor cell spheroids of two cell lines had higher gelatinolytic activity in less densely growing tumor cell groups than in the more densely growing ones. Our study provides considerable evidence that expression and activation of major MMPs is dependent on tumor cell density. This has a major impact on the biological behavior of tumor cells such as invasion and metastasis.

摘要

基质金属蛋白酶(MMPs)在与肿瘤细胞侵袭和生长相关的事件中起关键作用。因此,我们检测了12例浸润性乳腺癌患者的肿瘤组织样本中MMP-1、-2、-3和-9的表达及定位情况。通过免疫组织化学法进行检测。同时,对该样本通过原位酶谱法检测基质降解酶活性。此外,我们使用两种乳腺癌细胞系(MCF-7和MDA-MB-435)的球体模型,通过免疫组织化学和原位酶谱法检测MMP的表达及活性。通过免疫组织化学对组织样本中各种MMP进行半定量研究发现,与肿瘤中心紧密的肿瘤细胞复合体相比,在肿瘤周边肿瘤细胞生长较疏松处,MMP表达水平更高。原位明胶酶活性与这些观察结果一致,与肿瘤中心相比,在肿瘤周边显示出明显的活性。同样,两种细胞系的肿瘤细胞球体在生长较疏松的肿瘤细胞群中比在生长较密集的肿瘤细胞群中具有更高的明胶酶活性。我们的研究提供了大量证据表明主要MMP的表达和激活取决于肿瘤细胞密度。这对肿瘤细胞的生物学行为如侵袭和转移有重大影响。

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