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Lysyl Oxidase Family Proteins: Prospective Therapeutic Targets in Cancer

The lysyl oxidase (LOX) family, consisting of LOX and LOX-like proteins 1–4 (LOXL1–4), is responsible for the covalent crosslinking of collagen and elastin, thus maintaining the stability of the extracellular matrix (ECM) and functioning in maintaining connective tissue function, embryonic developme...

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Detalles Bibliográficos
Autores principales: Wang, Wei, Wang, Xiangjun, Yao, Feng, Huang, Chao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9602794/
https://www.ncbi.nlm.nih.gov/pubmed/36293126
http://dx.doi.org/10.3390/ijms232012270
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author Wang, Wei
Wang, Xiangjun
Yao, Feng
Huang, Chao
author_facet Wang, Wei
Wang, Xiangjun
Yao, Feng
Huang, Chao
author_sort Wang, Wei
collection PubMed
description The lysyl oxidase (LOX) family, consisting of LOX and LOX-like proteins 1–4 (LOXL1–4), is responsible for the covalent crosslinking of collagen and elastin, thus maintaining the stability of the extracellular matrix (ECM) and functioning in maintaining connective tissue function, embryonic development, and wound healing. Recent studies have found the aberrant expression or activity of the LOX family occurs in various types of cancer. It has been proved that the LOX family mainly performs tumor microenvironment (TME) remodeling function and is extensively involved in tumor invasion and metastasis, immunomodulation, proliferation, apoptosis, etc. With relevant translational research in progress, the LOX family is expected to be an effective target for tumor therapy. Here, we review the research progress of the LOX family in tumor progression and therapy to provide novel insights for future exploration of relevant tumor mechanism and new therapeutic targets.
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spelling pubmed-96027942022-10-27 Lysyl Oxidase Family Proteins: Prospective Therapeutic Targets in Cancer Wang, Wei Wang, Xiangjun Yao, Feng Huang, Chao Int J Mol Sci Review The lysyl oxidase (LOX) family, consisting of LOX and LOX-like proteins 1–4 (LOXL1–4), is responsible for the covalent crosslinking of collagen and elastin, thus maintaining the stability of the extracellular matrix (ECM) and functioning in maintaining connective tissue function, embryonic development, and wound healing. Recent studies have found the aberrant expression or activity of the LOX family occurs in various types of cancer. It has been proved that the LOX family mainly performs tumor microenvironment (TME) remodeling function and is extensively involved in tumor invasion and metastasis, immunomodulation, proliferation, apoptosis, etc. With relevant translational research in progress, the LOX family is expected to be an effective target for tumor therapy. Here, we review the research progress of the LOX family in tumor progression and therapy to provide novel insights for future exploration of relevant tumor mechanism and new therapeutic targets. MDPI 2022-10-14 /pmc/articles/PMC9602794/ /pubmed/36293126 http://dx.doi.org/10.3390/ijms232012270 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Wang, Wei
Wang, Xiangjun
Yao, Feng
Huang, Chao
Lysyl Oxidase Family Proteins: Prospective Therapeutic Targets in Cancer
title Lysyl Oxidase Family Proteins: Prospective Therapeutic Targets in Cancer
title_full Lysyl Oxidase Family Proteins: Prospective Therapeutic Targets in Cancer
title_fullStr Lysyl Oxidase Family Proteins: Prospective Therapeutic Targets in Cancer
title_full_unstemmed Lysyl Oxidase Family Proteins: Prospective Therapeutic Targets in Cancer
title_short Lysyl Oxidase Family Proteins: Prospective Therapeutic Targets in Cancer
title_sort lysyl oxidase family proteins: prospective therapeutic targets in cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9602794/
https://www.ncbi.nlm.nih.gov/pubmed/36293126
http://dx.doi.org/10.3390/ijms232012270
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