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测量结直肠癌中的明胶酶活性。

Measuring gelatinase activity in colorectal cancer.

作者信息

Baker E A, Leaper D J

机构信息

Professional Unit of Surgery, University Hospital of North Tees, Stockton on Tees, UK.

出版信息

Eur J Surg Oncol. 2002 Feb;28(1):24-9. doi: 10.1053/ejso.2001.1179.

Abstract

AIMS

Gelatinases (MMP-2, -9) are the most extensively studied MMPs in cancer. The aim of the study was to determine the levels of active and latent forms of the gelatinases in paired colorectal tumour and normal tissue ( n=77) and correlate these with pathological stage.

METHODS

Gelatinase levels were compared following the techniques of gelatin zymography (active and latent) and the novel gelatinase activity assays (total and endogenous/active).

RESULTS

Both latent and active MMP-2 and MMP-9 lysis bands (zymography) and both total (active and latent) MMP-9 and endogenous (active) MMP-9 and MMP-2 levels (activity assays) were greater in tumour than normal colorectal tissue. Total MMP-2 and MMP-9 levels as determined by activity assays correlated with both the Dukes staging (e.g. total MMP-9 in tumours: adenoma, 1.0 (0.3--3.6); Dukes A, 9.6 (2.4--35.4); Dukes B, 14.7 (1.5--103.9); Dukes C, 22.3 (2.2--57.9) and Dukes D, 37.4 (2.1--47.0) ng/mg protein) and with lymphatic invasion (e.g. total MMP-9; in tumours which had undergone lymphatic invasion, 22.7 (2.1--57.9) and those with no lymphatic invasion, 14.0 (1.5--103.9) ng/mg protein).

CONCLUSIONS

Both gelatinases were upregulated in tumour tissue, however total and not endogenous active levels correlated with the pathological stage of the tumour. Therefore gelatinases may only be activated when required for tumour invasion and metastasis.

摘要

目的

明胶酶(基质金属蛋白酶-2、-9)是癌症领域研究最为广泛的基质金属蛋白酶。本研究旨在测定77对结直肠肿瘤组织与正常组织中明胶酶的活性形式和潜在形式水平,并将其与病理分期相关联。

方法

采用明胶酶谱法(活性和潜在形式)及新型明胶酶活性测定法(总活性和内源性/活性)比较明胶酶水平。

结果

肿瘤组织中,潜在和活性的基质金属蛋白酶-2及基质金属蛋白酶-9裂解带(酶谱法),以及总(活性和潜在)基质金属蛋白酶-9、内源性(活性)基质金属蛋白酶-9和基质金属蛋白酶-2水平(活性测定法)均高于正常结直肠组织。活性测定法测定的总基质金属蛋白酶-2和基质金属蛋白酶-9水平与杜克分期相关(例如肿瘤中的总基质金属蛋白酶-9:腺瘤,1.0(0.3 - 3.6);杜克A期,9.6(2.4 - 35.4);杜克B期,14.7(1.5 - 103.9);杜克C期,22.3(2.2 - 57.9);杜克D期,37.4(2.1 - 47.0)ng/mg蛋白质),也与淋巴浸润相关(例如总基质金属蛋白酶-9;发生淋巴浸润的肿瘤中为22.7(2.1 - 57.9),未发生淋巴浸润的肿瘤中为14.0(1.5 - 103.9)ng/mg蛋白质)。

结论

肿瘤组织中两种明胶酶均上调,但总水平而非内源性活性水平与肿瘤的病理分期相关。因此,明胶酶可能仅在肿瘤侵袭和转移需要时才被激活。

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