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Molecular Mechanisms and Anticancer Therapeutic Strategies in Vasculogenic Mimicry

Vasculogenic mimicry (VM) is a vascular formation mechanism used by aggressive tumor cells. VM provides an alternative pathway for adequate blood perfusion and challenges the traditional angiogenesis mechanism that depends only on endothelial cells (ECs), as VM-forming tumor cells express a mixed en...

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Autores principales: Zhang, Xue, Zhang, Jigang, Zhou, Heming, Fan, Guorong, Li, Qin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6856738/
https://www.ncbi.nlm.nih.gov/pubmed/31772665
http://dx.doi.org/10.7150/jca.34171
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author Zhang, Xue
Zhang, Jigang
Zhou, Heming
Fan, Guorong
Li, Qin
author_facet Zhang, Xue
Zhang, Jigang
Zhou, Heming
Fan, Guorong
Li, Qin
author_sort Zhang, Xue
collection PubMed
description Vasculogenic mimicry (VM) is a vascular formation mechanism used by aggressive tumor cells. VM provides an alternative pathway for adequate blood perfusion and challenges the traditional angiogenesis mechanism that depends only on endothelial cells (ECs), as VM-forming tumor cells express a mixed endothelial/tumor phenotype. VM is closely correlated with tumor invasion, migration, and progression. Hence, anticancer therapeutic strategies targeting VM biogenesis are essential. It is widely acknowledged that the VM formation mechanism involves multiple pathways. The purpose of this review is to describe the potential molecular mechanisms related to different pathways and discuss the involvement of microRNAs (miRNAs), long non-coding RNAs (lncRNAs), and circular RNAs (circRNAs) in VM formation. Moreover, we discuss the significance of VM in clinical practice and present new anticancer therapeutic strategies that target VM.
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spelling pubmed-68567382019-11-26 Molecular Mechanisms and Anticancer Therapeutic Strategies in Vasculogenic Mimicry Zhang, Xue Zhang, Jigang Zhou, Heming Fan, Guorong Li, Qin J Cancer Review Vasculogenic mimicry (VM) is a vascular formation mechanism used by aggressive tumor cells. VM provides an alternative pathway for adequate blood perfusion and challenges the traditional angiogenesis mechanism that depends only on endothelial cells (ECs), as VM-forming tumor cells express a mixed endothelial/tumor phenotype. VM is closely correlated with tumor invasion, migration, and progression. Hence, anticancer therapeutic strategies targeting VM biogenesis are essential. It is widely acknowledged that the VM formation mechanism involves multiple pathways. The purpose of this review is to describe the potential molecular mechanisms related to different pathways and discuss the involvement of microRNAs (miRNAs), long non-coding RNAs (lncRNAs), and circular RNAs (circRNAs) in VM formation. Moreover, we discuss the significance of VM in clinical practice and present new anticancer therapeutic strategies that target VM. Ivyspring International Publisher 2019-10-18 /pmc/articles/PMC6856738/ /pubmed/31772665 http://dx.doi.org/10.7150/jca.34171 Text en © The author(s) This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Review
Zhang, Xue
Zhang, Jigang
Zhou, Heming
Fan, Guorong
Li, Qin
Molecular Mechanisms and Anticancer Therapeutic Strategies in Vasculogenic Mimicry
title Molecular Mechanisms and Anticancer Therapeutic Strategies in Vasculogenic Mimicry
title_full Molecular Mechanisms and Anticancer Therapeutic Strategies in Vasculogenic Mimicry
title_fullStr Molecular Mechanisms and Anticancer Therapeutic Strategies in Vasculogenic Mimicry
title_full_unstemmed Molecular Mechanisms and Anticancer Therapeutic Strategies in Vasculogenic Mimicry
title_short Molecular Mechanisms and Anticancer Therapeutic Strategies in Vasculogenic Mimicry
title_sort molecular mechanisms and anticancer therapeutic strategies in vasculogenic mimicry
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6856738/
https://www.ncbi.nlm.nih.gov/pubmed/31772665
http://dx.doi.org/10.7150/jca.34171
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