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Partial EMT in Squamous Cell Carcinoma: A Snapshot

In the process of cancer EMT, some subgroups of cancer cells simultaneously exhibit both mesenchymal and epithelial characteristics, a phenomenon termed partial EMT (pEMT). pEMT is a plastic state in which cells coexpress epithelial and mesenchymal markers. In squamous cell carcinoma (SCC), pEMT is...

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Autores principales: Liao, Chengcheng, Wang, Qian, An, Jiaxing, Long, Qian, Wang, Hui, Xiang, Meiling, Xiang, Mingli, Zhao, Yujie, Liu, Yulin, Liu, Jianguo, Guan, Xiaoyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8375241/
https://www.ncbi.nlm.nih.gov/pubmed/34421348
http://dx.doi.org/10.7150/ijbs.61566
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author Liao, Chengcheng
Wang, Qian
An, Jiaxing
Long, Qian
Wang, Hui
Xiang, Meiling
Xiang, Mingli
Zhao, Yujie
Liu, Yulin
Liu, Jianguo
Guan, Xiaoyan
author_facet Liao, Chengcheng
Wang, Qian
An, Jiaxing
Long, Qian
Wang, Hui
Xiang, Meiling
Xiang, Mingli
Zhao, Yujie
Liu, Yulin
Liu, Jianguo
Guan, Xiaoyan
author_sort Liao, Chengcheng
collection PubMed
description In the process of cancer EMT, some subgroups of cancer cells simultaneously exhibit both mesenchymal and epithelial characteristics, a phenomenon termed partial EMT (pEMT). pEMT is a plastic state in which cells coexpress epithelial and mesenchymal markers. In squamous cell carcinoma (SCC), pEMT is regulated, and the phenotype is maintained via the HIPPO pathway, NOTCH pathway and TGF-β pathways and by microRNAs, lncRNAs and the cancer microenvironment (CME); thus, SCC exhibits aggressive tumorigenic properties and high stemness, which leads collective migration and therapy resistance. Few studies have reported therapeutic interventions to address cells that have undergone pEMT, and this approach may be an effective way to inhibit the plasticity, drug resistance and metastatic potential of SCC.
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spelling pubmed-83752412021-08-19 Partial EMT in Squamous Cell Carcinoma: A Snapshot Liao, Chengcheng Wang, Qian An, Jiaxing Long, Qian Wang, Hui Xiang, Meiling Xiang, Mingli Zhao, Yujie Liu, Yulin Liu, Jianguo Guan, Xiaoyan Int J Biol Sci Review In the process of cancer EMT, some subgroups of cancer cells simultaneously exhibit both mesenchymal and epithelial characteristics, a phenomenon termed partial EMT (pEMT). pEMT is a plastic state in which cells coexpress epithelial and mesenchymal markers. In squamous cell carcinoma (SCC), pEMT is regulated, and the phenotype is maintained via the HIPPO pathway, NOTCH pathway and TGF-β pathways and by microRNAs, lncRNAs and the cancer microenvironment (CME); thus, SCC exhibits aggressive tumorigenic properties and high stemness, which leads collective migration and therapy resistance. Few studies have reported therapeutic interventions to address cells that have undergone pEMT, and this approach may be an effective way to inhibit the plasticity, drug resistance and metastatic potential of SCC. Ivyspring International Publisher 2021-07-13 /pmc/articles/PMC8375241/ /pubmed/34421348 http://dx.doi.org/10.7150/ijbs.61566 Text en © The author(s) https://creativecommons.org/licenses/by/4.0/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
Liao, Chengcheng
Wang, Qian
An, Jiaxing
Long, Qian
Wang, Hui
Xiang, Meiling
Xiang, Mingli
Zhao, Yujie
Liu, Yulin
Liu, Jianguo
Guan, Xiaoyan
Partial EMT in Squamous Cell Carcinoma: A Snapshot
title Partial EMT in Squamous Cell Carcinoma: A Snapshot
title_full Partial EMT in Squamous Cell Carcinoma: A Snapshot
title_fullStr Partial EMT in Squamous Cell Carcinoma: A Snapshot
title_full_unstemmed Partial EMT in Squamous Cell Carcinoma: A Snapshot
title_short Partial EMT in Squamous Cell Carcinoma: A Snapshot
title_sort partial emt in squamous cell carcinoma: a snapshot
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8375241/
https://www.ncbi.nlm.nih.gov/pubmed/34421348
http://dx.doi.org/10.7150/ijbs.61566
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