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基质金属蛋白酶-1、-2和-3在鳞状细胞癌及光化性角化病中的表达

Expression of matrix metalloproteinase-1, -2 and -3 in squamous cell carcinoma and actinic keratosis.

作者信息

Tsukifuji R, Tagawa K, Hatamochi A, Shinkai H

机构信息

Division of Dermatology, National Chiba Hospital, Japan.

出版信息

Br J Cancer. 1999 Jun;80(7):1087-91. doi: 10.1038/sj.bjc.6690468.

DOI:10.1038/sj.bjc.6690468
PMID:10362121
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2363037/
Abstract

Matrix metalloproteinase (MMP) plays an important role in extracellular matrix degradation associated with cancer invasion. An expression of MMP-1 (interstitial collagenase), MMP-2 (72-kDa type IV collagenase) and MMP-3 (stromelysin-1) was investigated in squamous cell carcinoma (SCC) and its precancerous condition, actinic keratosis (AK), using in situ hybridization techniques. MMP-1 mRNA was detected in tumour cells and/or in stromal cells in all cases of SCC, four of six AKs adjacent to SCC and four of 16 AKs. MMP-2 and MMP-3 mRNAs were detected in SCC but not in AK. The expression of MMP-3 correlated to that of MMP-1 (P = 0.03) localized at the tumour mass and stroma of the invasive area, while MMP-2 mRNA was detected widely throughout the stroma independent of MMP-1 expression. Our results indicated that the expression of MMP-1, -2 and -3 showed different localization patterns, suggesting a unique role of each MMP in tumour progression. Moreover, MMP-1 expression could be an early event in the development of SCC, and AK demonstrating MMP-1 mRNA, might be in a more advanced dysplastic state, progressing to SCC.

摘要

基质金属蛋白酶(MMP)在与癌症侵袭相关的细胞外基质降解中起重要作用。使用原位杂交技术,研究了基质金属蛋白酶-1(间质胶原酶)、基质金属蛋白酶-2(72 kDa IV型胶原酶)和基质金属蛋白酶-3(基质溶解素-1)在鳞状细胞癌(SCC)及其癌前病变光化性角化病(AK)中的表达情况。在所有SCC病例、6例与SCC相邻的AK中的4例以及16例AK中的4例中,在肿瘤细胞和/或基质细胞中检测到基质金属蛋白酶-1 mRNA。在SCC中检测到基质金属蛋白酶-2和基质金属蛋白酶-3 mRNA,但在AK中未检测到。基质金属蛋白酶-3的表达与位于侵袭区域肿瘤块和基质中的基质金属蛋白酶-1的表达相关(P = 0.03),而基质金属蛋白酶-2 mRNA在整个基质中广泛检测到,与基质金属蛋白酶-1的表达无关。我们的结果表明,基质金属蛋白酶-1、-2和-3的表达呈现不同的定位模式,提示每种基质金属蛋白酶在肿瘤进展中具有独特作用。此外,基质金属蛋白酶-1的表达可能是SCC发生过程中的早期事件,显示基质金属蛋白酶-1 mRNA的AK可能处于更高级的发育异常状态,进展为SCC。

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