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Targeting Lysyl Oxidase Family Meditated Matrix Cross-Linking as an Anti-Stromal Therapy in Solid Tumours

SIMPLE SUMMARY: To improve efficacy of solid cancer treatment, efforts have shifted towards targeting both the cancer cells and the surrounding tumour tissue they grow in. The lysyl oxidase (LOX) family of enzymes underpin the fibrotic remodeling of the tumour microenvironment to promote both cancer...

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Autores principales: Setargew, Yordanos F.I., Wyllie, Kaitlin, Grant, Rhiannon D., Chitty, Jessica L., Cox, Thomas R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7865543/
https://www.ncbi.nlm.nih.gov/pubmed/33513979
http://dx.doi.org/10.3390/cancers13030491
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author Setargew, Yordanos F.I.
Wyllie, Kaitlin
Grant, Rhiannon D.
Chitty, Jessica L.
Cox, Thomas R.
author_facet Setargew, Yordanos F.I.
Wyllie, Kaitlin
Grant, Rhiannon D.
Chitty, Jessica L.
Cox, Thomas R.
author_sort Setargew, Yordanos F.I.
collection PubMed
description SIMPLE SUMMARY: To improve efficacy of solid cancer treatment, efforts have shifted towards targeting both the cancer cells and the surrounding tumour tissue they grow in. The lysyl oxidase (LOX) family of enzymes underpin the fibrotic remodeling of the tumour microenvironment to promote both cancer growth, spread throughout the body and modulate response to therapies. This review examines how the lysyl oxidase family is involved in tumour development, how they can be targeted, and their potential as diagnostic and prognostic biomarkers in solid tumours. ABSTRACT: The lysyl oxidase (LOX) family of enzymes are a major driver in the biogenesis of desmoplastic matrix at the primary tumour and secondary metastatic sites. With the increasing interest in and development of anti-stromal therapies aimed at improving clinical outcomes of cancer patients, the Lox family has emerged as a potentially powerful clinical target. This review examines how lysyl oxidase family dysregulation in solid cancers contributes to disease progression and poor patient outcomes, as well as an evaluation of the preclinical landscape of LOX family targeting therapeutics. We also discuss the suitability of the LOX family as a diagnostic and/or prognostic marker in solid tumours.
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spelling pubmed-78655432021-02-07 Targeting Lysyl Oxidase Family Meditated Matrix Cross-Linking as an Anti-Stromal Therapy in Solid Tumours Setargew, Yordanos F.I. Wyllie, Kaitlin Grant, Rhiannon D. Chitty, Jessica L. Cox, Thomas R. Cancers (Basel) Review SIMPLE SUMMARY: To improve efficacy of solid cancer treatment, efforts have shifted towards targeting both the cancer cells and the surrounding tumour tissue they grow in. The lysyl oxidase (LOX) family of enzymes underpin the fibrotic remodeling of the tumour microenvironment to promote both cancer growth, spread throughout the body and modulate response to therapies. This review examines how the lysyl oxidase family is involved in tumour development, how they can be targeted, and their potential as diagnostic and prognostic biomarkers in solid tumours. ABSTRACT: The lysyl oxidase (LOX) family of enzymes are a major driver in the biogenesis of desmoplastic matrix at the primary tumour and secondary metastatic sites. With the increasing interest in and development of anti-stromal therapies aimed at improving clinical outcomes of cancer patients, the Lox family has emerged as a potentially powerful clinical target. This review examines how lysyl oxidase family dysregulation in solid cancers contributes to disease progression and poor patient outcomes, as well as an evaluation of the preclinical landscape of LOX family targeting therapeutics. We also discuss the suitability of the LOX family as a diagnostic and/or prognostic marker in solid tumours. MDPI 2021-01-27 /pmc/articles/PMC7865543/ /pubmed/33513979 http://dx.doi.org/10.3390/cancers13030491 Text en © 2021 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Setargew, Yordanos F.I.
Wyllie, Kaitlin
Grant, Rhiannon D.
Chitty, Jessica L.
Cox, Thomas R.
Targeting Lysyl Oxidase Family Meditated Matrix Cross-Linking as an Anti-Stromal Therapy in Solid Tumours
title Targeting Lysyl Oxidase Family Meditated Matrix Cross-Linking as an Anti-Stromal Therapy in Solid Tumours
title_full Targeting Lysyl Oxidase Family Meditated Matrix Cross-Linking as an Anti-Stromal Therapy in Solid Tumours
title_fullStr Targeting Lysyl Oxidase Family Meditated Matrix Cross-Linking as an Anti-Stromal Therapy in Solid Tumours
title_full_unstemmed Targeting Lysyl Oxidase Family Meditated Matrix Cross-Linking as an Anti-Stromal Therapy in Solid Tumours
title_short Targeting Lysyl Oxidase Family Meditated Matrix Cross-Linking as an Anti-Stromal Therapy in Solid Tumours
title_sort targeting lysyl oxidase family meditated matrix cross-linking as an anti-stromal therapy in solid tumours
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7865543/
https://www.ncbi.nlm.nih.gov/pubmed/33513979
http://dx.doi.org/10.3390/cancers13030491
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