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1型膜基质金属蛋白酶介导的人甲状腺乳头状癌中前明胶酶A的生成及激活增强

Enhanced production and activation of progelatinase A mediated by membrane-type 1 matrix metalloproteinase in human papillary thyroid carcinomas.

作者信息

Nakamura H, Ueno H, Yamashita K, Shimada T, Yamamoto E, Noguchi M, Fujimoto N, Sato H, Seiki M, Okada Y

机构信息

Department of Pathology, School of Medicine, Keio University, Tokyo, Japan.

出版信息

Cancer Res. 1999 Jan 15;59(2):467-73.

PMID:9927064
Abstract

Matrix metalloproteinases (MMPs) are believed to be involved in the invasion and metastasis of various human carcinomas. In the present study, the production levels of seven different MMPs (MMP-1, -2, -3, -7, -8, -9, and -13), the activation of the zymogen of MMP-2 (proMMP-2), the expression of membrane-type MMPs (MT1-, MT2-, and MT3-MMPs), and the tissue localization of the activated enzyme were examined in human invasive papillary thyroid carcinomas. Sandwich enzyme immunoassays revealed that among the MMPs examined, only the MMP-2 production level is significantly enhanced in the carcinoma tissues compared with the follicular adenoma and normal control thyroid tissues. Gelatin zymography indicated that the proMMP-2 activation ratio is considerably higher in carcinomas with lymph node metastasis than it is in those without metastasis, follicular adenomas, or normal controls (P < 0.01). Northern blot analysis of the expression of MT1-, MT2-, and MT3-MMPs, which are known to activate proMMP-2 in vitro, demonstrated the predominant expression of MT1-MMP mRNA in the carcinoma tissues (15 of 15 cases), whereas MT2-MMP expression was confined to 26% of the cases (4 of 15 cases), and no consistent expression of MT3-MMP was observed. MTI-MMP mRNA expression levels correlated with the proMMP-2 activation ratio (r = 0.692; P < 0.01), but such a correlation was not obtained with MT2-MMP. There was also a direct correlation between MT1-MMP expression and lymph node metastasis (P < 0.05). In situ hybridization indicated that both carcinoma and stromal cells express MT1-MMP transcripts (five of six cases). MT1-MMP was also immunolocalized to carcinoma and stromal cells in all of the carcinoma samples (26 of 26 cases), which were positive for MMP-2. In situ zymography indicated definite gelatinolytic activity in the carcinoma cell nests, which was abolished by incubation of the carcinoma samples with a synthetic MMP inhibitor before the reaction. These results suggest for the first time that among seven different MMPs, the production of proMMP-2 and its MT1-MMP-mediated activation in the carcinoma cell nests play an important role in the lymph node metastasis of human invasive papillary thyroid carcinomas.

摘要

基质金属蛋白酶(MMPs)被认为参与了多种人类癌症的侵袭和转移。在本研究中,检测了7种不同MMPs(MMP-1、-2、-3、-7、-8、-9和-13)的产生水平、MMP-2酶原(proMMP-2)的激活、膜型MMPs(MT1-MMP、MT2-MMP和MT3-MMP)的表达以及活化酶在人侵袭性乳头状甲状腺癌中的组织定位。夹心酶免疫分析显示,在所检测的MMPs中,与滤泡性腺瘤和正常对照甲状腺组织相比,仅癌组织中的MMP-2产生水平显著升高。明胶酶谱分析表明,有淋巴结转移的癌组织中proMMP-2的激活率显著高于无转移的癌组织、滤泡性腺瘤或正常对照(P<0.01)。已知MT1-MMP、MT2-MMP和MT3-MMP在体外可激活proMMP-2,对其表达进行Northern印迹分析显示,癌组织中MT1-MMP mRNA呈优势表达(15例中有15例),而MT2-MMP表达仅见于26%的病例(15例中有4例),未观察到MT3-MMP的一致性表达。MT1-MMP mRNA表达水平与proMMP-2激活率相关(r=0.692;P<0.01),而与MT2-MMP无此相关性。MT1-MMP表达与淋巴结转移之间也存在直接相关性(P<0.05)。原位杂交表明,癌组织和基质细胞均表达MT1-MMP转录本(6例中有5例)。在所有MMP-2阳性的癌组织样本(26例中有26例)中,MT1-MMP也定位于癌组织和基质细胞。原位酶谱分析表明,癌细胞巢中有明确的明胶溶解活性,在反应前用合成MMP抑制剂孵育癌组织样本可消除该活性。这些结果首次表明,在7种不同的MMPs中,癌组织中proMMP-2的产生及其MT1-MMP介导的激活在人侵袭性乳头状甲状腺癌的淋巴结转移中起重要作用。

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