Membrane-Type Matrix Metalloproteinases (MT-MMPs) in Tumor Metastasis1 (original) (raw)

Journal Article

,

Department of Molecular Virology and Oncology, Cancer Research Institute, Kanazawa University

13-1 Takara-machi, Kanazawa 920

2To whom correspondence should be addressed. Fax: + 81-762-60-7840

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Department of Molecular Virology and Oncology, Cancer Research Institute, Kanazawa University

13-1 Takara-machi, Kanazawa 920

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1This work was supported by the Special Coordination Fund for Promoting Science and Technology from the Ministry of Science and Technology of Japan; by a Grant-in-Aid from the Ministry of Education, Science, and Culture of Japan.

Author Notes

Received:

27 September 1995

Published:

01 February 1996

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Abstract

Activated gelatinase A is reportedly associated with tumor spread. We identified novel matrix metalloproteinases that localize on the cell surface and mediate the activation of progelatinase A. Thus, these progelatinase A activators were named membrane-type matrix metalloproteinase-1 and −2 (MT-MMP-1 and −2, respectively). MT-MMP-1 is overexpressed in malignant tumor tissues, including lung and stomach carcinomas that contain activated gelatinase A. This suggests that MT-MMP-1 is associated with the activation of progelatinase A in these tumor tissues. The expression of MT-MMP-1 also induced binding of gelatinase A to the cell surface by functioning as a receptor. The cell surface localization of proteinases has advantages over pericellular proteolysis. MT-MMP -1 and its family may play a central role in the cell surface localization and activation of progelatinase A and via this mechanism, tumor cell use exogenous progelatinase A to mediate the proteolysis associated with invasion and metastasis.

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Author notes

1This work was supported by the Special Coordination Fund for Promoting Science and Technology from the Ministry of Science and Technology of Japan; by a Grant-in-Aid from the Ministry of Education, Science, and Culture of Japan.

© by the Journal of Biochemistry

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