Literature DB >> 3036719

The relationship of collagenolytic activity to stage of human colorectal carcinoma.

T Irimura, T Yamori, S C Bennett, D M Ota, K R Cleary.   

Abstract

Collagenolytic enzymes produced by tumor cells are believed to play a significant role in the destruction of surrounding normal tissue and, in certain experimental animal systems, the ability of tumor cells to degrade type-IV collagen (basement membrane collagen) correlates positively with those cells' metastatic capacity. We measured collagenolytic activity levels of extracts from freshly excised colorectal carcinoma tissues and of conditioned media from primary organ culture (total of 114 tissues from 53 patients) by using purified radiolabelled type-I (rat tail) and type-IV (mouse Engelbreth-Holm-Swarm [EHS] sarcoma) collagens. Both type-IV and type-I collagenolytic activity levels of extracts from tumor and adjacent mucosa ranged from less than 1 to 80 ng/hr/mg wet tissue, and no significant differences between mucosa and carcinoma tissues were observed. In conditioned media, the type-IV collagenolytic activity was low for normal mucosa and benign tumors and slightly higher for carcinoma than for mucosa. In 5 of 32 primary tumors, collagenolytic activity levels were 2-5 times higher than in the rest of the tumors and mucosal tissues. There were no significant differences in collagenolytic activity levels of conditioned media and tissue extract from colorectal carcinoma of different Dukes' stages. Deep and superficial areas of primary tumors released similar type-IV collagenolytic activity levels, suggesting that there was little intratumoral heterogeneity in the release of this enzyme.

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Year:  1987        PMID: 3036719     DOI: 10.1002/ijc.2910400106

Source DB:  PubMed          Journal:  Int J Cancer        ISSN: 0020-7136            Impact factor:   7.396


  8 in total

1.  In situ hybridization studies of metalloproteinases 2 and 9 and TIMP-1 and TIMP-2 expression in human prostate cancer.

Authors:  M Wood; K Fudge; J L Mohler; A R Frost; F Garcia; M Wang; M E Stearns
Journal:  Clin Exp Metastasis       Date:  1997-05       Impact factor: 5.150

2.  Alendronate blocks metalloproteinase secretion and bone collagen I release by PC-3 ML cells in SCID mice.

Authors:  M E Stearns; M Wang
Journal:  Clin Exp Metastasis       Date:  1998-11       Impact factor: 5.150

Review 3.  Cathepsin B and other proteases in human colorectal carcinoma.

Authors:  J M Jessup
Journal:  Am J Pathol       Date:  1994-08       Impact factor: 4.307

4.  Alendronate blocks TGF-beta1 stimulated collagen 1 degradation by human prostate PC-3 ML cells.

Authors:  M E Stearns
Journal:  Clin Exp Metastasis       Date:  1998-05       Impact factor: 5.150

5.  Interstitial collagenase gene expression in colonic neoplasia.

Authors:  S T Gray; K Yun; T Motoori; Y M Kuys
Journal:  Am J Pathol       Date:  1993-09       Impact factor: 4.307

6.  Sequential degradation of interstitial collagen by metalloproteinases extracted from tumors of murine ascites hepatomas.

Authors:  H Koita; K Nabeshima; T Inoue; M Koono
Journal:  Clin Exp Metastasis       Date:  1991 Sep-Oct       Impact factor: 5.150

7.  Morphological distribution of μ chains and cd15 receptors in colorectal polyp and adenocarcinoma specimens.

Authors:  Caterina Defendenti; Fabiola Atzeni; Anna Maria Croce; Elena Mussani; Simone Saibeni; Simona Bollani; Silvia Grosso; Piero Luigi Almasio; Savino Bruno; Piercarlo Sarzi-Puttini
Journal:  BMC Clin Pathol       Date:  2013-03-01

8.  Production of matrix metalloproteinase 9 (92-kDa gelatinase) by human oesophageal squamous cell carcinoma in response to epidermal growth factor.

Authors:  I Shima; Y Sasaguri; J Kusukawa; R Nakano; H Yamana; H Fujita; T Kakegawa; M Morimatsu
Journal:  Br J Cancer       Date:  1993-04       Impact factor: 7.640

  8 in total

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