人结肠原发肿瘤转移灶中IV型胶原降解活性增高。

Invasion & metastasis Pub Date : 1997-01-01
G Karakiulakis, C Papanikolaou, S M Jankovic, A Aletras, E Papakonstantinou, E Vretou, V Mirtsou-Fidani
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引用次数: 0

摘要

特异性基质金属蛋白酶(MMPs)的分泌被认为是肿瘤细胞侵袭和转移的先决条件。在本研究中,我们研究了IV型胶原降解活性在人类结肠原发肿瘤中的表达与肿瘤级别的关系,并与发生转移的活性表达进行了比较。我们观察到IV型胶原降解活性(MMP-2和MMP-9),通过离子交换、凝胶过滤和亲和层析纯化,并用明胶酶谱法表征,与肿瘤分级相关。此外,在确定为源自结肠原发肿瘤的转移瘤的手术标本中,我们观察到,相对于原发肿瘤,酶活性显着增强。当靶向MMPs作为预防癌症进展的治疗干预措施时,应考虑这一观察结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Increased type IV collagen-degrading activity in metastases originating from primary tumors of the human colon.

The secretion of specific matrix metalloproteinases (MMPs) is considered a prerequisite step for tumor cell invasion and metastasis. In the present study we investigated the expression of type IV collagen-degrading activity in primary tumors of the human colon in correlation to tumor grade and in comparison to activity expressed in arising metastases. We observed that type IV collagen-degrading activity (MMP-2 and MMP-9), purified by ion exchange, gel filtration and affinity chromatography and characterized by gelatin zymography, correlates to tumor grade. Furthermore, in surgical specimens identified as metastases originating from primary tumors of the colon, we observed that enzyme activity was significantly enhanced, relatively to that identified in the primary tumor. This observation should be considered when targeting MMPs as a therapeutic intervention to prevent cancer progression.

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