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Interplay of EMT and CSC in Cancer and the Potential Therapeutic Strategies

The mechanism of epithelial-mesenchymal transition (EMT) consists of the cellular phenotypic transition from epithelial to mesenchymal status. The cells exhibiting EMT exist in cancer stem cell (CSC) population, which is involved in drug resistance. CSCs demonstrating EMT feature remain after cancer...

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Detalles Bibliográficos
Autores principales: Tanabe, Shihori, Quader, Sabina, Cabral, Horacio, Ono, Ryuichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7311659/
https://www.ncbi.nlm.nih.gov/pubmed/32625096
http://dx.doi.org/10.3389/fphar.2020.00904
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author Tanabe, Shihori
Quader, Sabina
Cabral, Horacio
Ono, Ryuichi
author_facet Tanabe, Shihori
Quader, Sabina
Cabral, Horacio
Ono, Ryuichi
author_sort Tanabe, Shihori
collection PubMed
description The mechanism of epithelial-mesenchymal transition (EMT) consists of the cellular phenotypic transition from epithelial to mesenchymal status. The cells exhibiting EMT exist in cancer stem cell (CSC) population, which is involved in drug resistance. CSCs demonstrating EMT feature remain after cancer treatment, which leads to drug resistance, recurrence, metastasis and malignancy of cancer. In this context, the recent advance of nanotechnology in the medical application has ascended the possibility to target CSCs using nanomedicines. In this review article, we focused on the mechanism of CSCs and EMT, especially into the signaling pathways in EMT, regulation of EMT and CSCs by microRNAs and nanomedicine-based approaches to target CSCs.
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spelling pubmed-73116592020-07-02 Interplay of EMT and CSC in Cancer and the Potential Therapeutic Strategies Tanabe, Shihori Quader, Sabina Cabral, Horacio Ono, Ryuichi Front Pharmacol Pharmacology The mechanism of epithelial-mesenchymal transition (EMT) consists of the cellular phenotypic transition from epithelial to mesenchymal status. The cells exhibiting EMT exist in cancer stem cell (CSC) population, which is involved in drug resistance. CSCs demonstrating EMT feature remain after cancer treatment, which leads to drug resistance, recurrence, metastasis and malignancy of cancer. In this context, the recent advance of nanotechnology in the medical application has ascended the possibility to target CSCs using nanomedicines. In this review article, we focused on the mechanism of CSCs and EMT, especially into the signaling pathways in EMT, regulation of EMT and CSCs by microRNAs and nanomedicine-based approaches to target CSCs. Frontiers Media S.A. 2020-06-17 /pmc/articles/PMC7311659/ /pubmed/32625096 http://dx.doi.org/10.3389/fphar.2020.00904 Text en Copyright © 2020 Tanabe, Quader, Cabral and Ono http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Tanabe, Shihori
Quader, Sabina
Cabral, Horacio
Ono, Ryuichi
Interplay of EMT and CSC in Cancer and the Potential Therapeutic Strategies
title Interplay of EMT and CSC in Cancer and the Potential Therapeutic Strategies
title_full Interplay of EMT and CSC in Cancer and the Potential Therapeutic Strategies
title_fullStr Interplay of EMT and CSC in Cancer and the Potential Therapeutic Strategies
title_full_unstemmed Interplay of EMT and CSC in Cancer and the Potential Therapeutic Strategies
title_short Interplay of EMT and CSC in Cancer and the Potential Therapeutic Strategies
title_sort interplay of emt and csc in cancer and the potential therapeutic strategies
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7311659/
https://www.ncbi.nlm.nih.gov/pubmed/32625096
http://dx.doi.org/10.3389/fphar.2020.00904
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