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Kallikrein-Related Peptidases in Prostate Cancer: From Molecular Function to Clinical Application
Prostate cancer is a leading contributor to male cancer-related deaths worldwide. Kallikrein-related peptidases (KLKs) are serine proteases that exhibit deregulated expression in prostate cancer, with KLK3, or prostate specific antigen (PSA), being the widely-employed clinical biomarker for prostate...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Communications and Publications Division (CPD) of the IFCC
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4975200/ https://www.ncbi.nlm.nih.gov/pubmed/27683474 |
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author | Fuhrman-Luck, Ruth A. Loessner, Daniela Clements, Judith A. |
author_facet | Fuhrman-Luck, Ruth A. Loessner, Daniela Clements, Judith A. |
author_sort | Fuhrman-Luck, Ruth A. |
collection | PubMed |
description | Prostate cancer is a leading contributor to male cancer-related deaths worldwide. Kallikrein-related peptidases (KLKs) are serine proteases that exhibit deregulated expression in prostate cancer, with KLK3, or prostate specific antigen (PSA), being the widely-employed clinical biomarker for prostate cancer. Other KLKs, such as KLK2, show promise as prostate cancer biomarkers and, additionally, their altered expression has been utilised for the design of KLK-targeted therapies. There is also a large body of in vitro and in vivo evidence supporting their role in cancer-related processes. Here, we review the literature on studies to date investigating the potential of other KLKs, in addition to PSA, as biomarkers and in therapeutic options, as well as their current known functional roles in cancer progression. Increased knowledge of these KLK-mediated functions, including degradation of the extracellular matrix, local invasion, cancer cell proliferation, interactions with fibroblasts, angiogenesis, migration, bone metastasis and tumour growth in vivo, may help define new roles as prognostic biomarkers and novel therapeutic targets for this cancer. |
format | Online Article Text |
id | pubmed-4975200 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | The Communications and Publications Division (CPD) of the IFCC |
record_format | MEDLINE/PubMed |
spelling | pubmed-49752002016-09-28 Kallikrein-Related Peptidases in Prostate Cancer: From Molecular Function to Clinical Application Fuhrman-Luck, Ruth A. Loessner, Daniela Clements, Judith A. EJIFCC Research Article Prostate cancer is a leading contributor to male cancer-related deaths worldwide. Kallikrein-related peptidases (KLKs) are serine proteases that exhibit deregulated expression in prostate cancer, with KLK3, or prostate specific antigen (PSA), being the widely-employed clinical biomarker for prostate cancer. Other KLKs, such as KLK2, show promise as prostate cancer biomarkers and, additionally, their altered expression has been utilised for the design of KLK-targeted therapies. There is also a large body of in vitro and in vivo evidence supporting their role in cancer-related processes. Here, we review the literature on studies to date investigating the potential of other KLKs, in addition to PSA, as biomarkers and in therapeutic options, as well as their current known functional roles in cancer progression. Increased knowledge of these KLK-mediated functions, including degradation of the extracellular matrix, local invasion, cancer cell proliferation, interactions with fibroblasts, angiogenesis, migration, bone metastasis and tumour growth in vivo, may help define new roles as prognostic biomarkers and novel therapeutic targets for this cancer. The Communications and Publications Division (CPD) of the IFCC 2014-10-24 /pmc/articles/PMC4975200/ /pubmed/27683474 Text en Copyright © 2014 International Federation of Clinical Chemistry and Laboratory Medicine (IFCC). All rights reserved. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Fuhrman-Luck, Ruth A. Loessner, Daniela Clements, Judith A. Kallikrein-Related Peptidases in Prostate Cancer: From Molecular Function to Clinical Application |
title | Kallikrein-Related Peptidases in Prostate Cancer: From Molecular Function to Clinical Application |
title_full | Kallikrein-Related Peptidases in Prostate Cancer: From Molecular Function to Clinical Application |
title_fullStr | Kallikrein-Related Peptidases in Prostate Cancer: From Molecular Function to Clinical Application |
title_full_unstemmed | Kallikrein-Related Peptidases in Prostate Cancer: From Molecular Function to Clinical Application |
title_short | Kallikrein-Related Peptidases in Prostate Cancer: From Molecular Function to Clinical Application |
title_sort | kallikrein-related peptidases in prostate cancer: from molecular function to clinical application |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4975200/ https://www.ncbi.nlm.nih.gov/pubmed/27683474 |
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