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TIMP-3 as a therapeutic target for cancer

Tissue inhibitor of metalloproteinase-3 (TIMP-3), a secreted glycoprotein, plays an important role in carcinogenesis. It can bind to many proteinases to suppress their activity and thus protect the extracellular matrix from degradation. TIMP-3 may have many anticancer properties, including apoptosis...

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Detalles Bibliográficos
Autores principales: Su, Chun-Wen, Lin, Chiao-Wen, Yang, Wei-En, Yang, Shun-Fa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6637839/
https://www.ncbi.nlm.nih.gov/pubmed/31360238
http://dx.doi.org/10.1177/1758835919864247
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author Su, Chun-Wen
Lin, Chiao-Wen
Yang, Wei-En
Yang, Shun-Fa
author_facet Su, Chun-Wen
Lin, Chiao-Wen
Yang, Wei-En
Yang, Shun-Fa
author_sort Su, Chun-Wen
collection PubMed
description Tissue inhibitor of metalloproteinase-3 (TIMP-3), a secreted glycoprotein, plays an important role in carcinogenesis. It can bind to many proteinases to suppress their activity and thus protect the extracellular matrix from degradation. TIMP-3 may have many anticancer properties, including apoptosis induction and antiproliferative, antiangiogenic, and antimetastatic activities. This review summarizes the structure, proteinase inhibition ability, genetic and epigenetic regulation, cancer therapy potential, and contribution to cancer development of TIMP-3. Furthermore, in this review we discuss its potential as a biomarker for predicting cancer progression and the current state of drugs that target TIMP-3, either alone or in combination with clinical treatment. In conclusion, TIMP-3 can be a biomarker of cancer and a potential target for cancer therapy. This review article can serve as a basis to understand how to modulate TIMP-3 levels as a drug target of cancers.
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spelling pubmed-66378392019-07-29 TIMP-3 as a therapeutic target for cancer Su, Chun-Wen Lin, Chiao-Wen Yang, Wei-En Yang, Shun-Fa Ther Adv Med Oncol Review Tissue inhibitor of metalloproteinase-3 (TIMP-3), a secreted glycoprotein, plays an important role in carcinogenesis. It can bind to many proteinases to suppress their activity and thus protect the extracellular matrix from degradation. TIMP-3 may have many anticancer properties, including apoptosis induction and antiproliferative, antiangiogenic, and antimetastatic activities. This review summarizes the structure, proteinase inhibition ability, genetic and epigenetic regulation, cancer therapy potential, and contribution to cancer development of TIMP-3. Furthermore, in this review we discuss its potential as a biomarker for predicting cancer progression and the current state of drugs that target TIMP-3, either alone or in combination with clinical treatment. In conclusion, TIMP-3 can be a biomarker of cancer and a potential target for cancer therapy. This review article can serve as a basis to understand how to modulate TIMP-3 levels as a drug target of cancers. SAGE Publications 2019-07-16 /pmc/articles/PMC6637839/ /pubmed/31360238 http://dx.doi.org/10.1177/1758835919864247 Text en © The Author(s), 2019 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Review
Su, Chun-Wen
Lin, Chiao-Wen
Yang, Wei-En
Yang, Shun-Fa
TIMP-3 as a therapeutic target for cancer
title TIMP-3 as a therapeutic target for cancer
title_full TIMP-3 as a therapeutic target for cancer
title_fullStr TIMP-3 as a therapeutic target for cancer
title_full_unstemmed TIMP-3 as a therapeutic target for cancer
title_short TIMP-3 as a therapeutic target for cancer
title_sort timp-3 as a therapeutic target for cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6637839/
https://www.ncbi.nlm.nih.gov/pubmed/31360238
http://dx.doi.org/10.1177/1758835919864247
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