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Cancer stem cells: A comprehensive review on identification and therapeutic implications

Cancer stem cells (CSCs) are distinct subpopulations of tumor cells that possess the ability for perpetual self-renewal and proliferation. They produce downstream progenitor cells and cancer cells that drive tumor growth. Studies of many cancer types including oral squamous cell carcinoma (OSCC) hav...

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Detalles Bibliográficos
Autores principales: Varun, BR, Jayanthi, P, Ramani, Pratibha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7269290/
https://www.ncbi.nlm.nih.gov/pubmed/32508482
http://dx.doi.org/10.4103/jomfp.JOMFP_336_19
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author Varun, BR
Jayanthi, P
Ramani, Pratibha
author_facet Varun, BR
Jayanthi, P
Ramani, Pratibha
author_sort Varun, BR
collection PubMed
description Cancer stem cells (CSCs) are distinct subpopulations of tumor cells that possess the ability for perpetual self-renewal and proliferation. They produce downstream progenitor cells and cancer cells that drive tumor growth. Studies of many cancer types including oral squamous cell carcinoma (OSCC) have identified CSCs using specific markers, but it is still unclear as to where in the stem cell hierarchy these markers fall. This is compounded further by the presence of multiple CSC subtypes within OSCC, making investigation reliant on the use of multiple markers. This review paper focuses on the current knowledge in CSC markers including OCT4, SOX2, NANOG, aldehyde dehydrogenase 1, CD44, CD24, CD133 and Musashi-1, highlighting their use and validity in OSCC CSC research.
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spelling pubmed-72692902020-06-05 Cancer stem cells: A comprehensive review on identification and therapeutic implications Varun, BR Jayanthi, P Ramani, Pratibha J Oral Maxillofac Pathol Review Article Cancer stem cells (CSCs) are distinct subpopulations of tumor cells that possess the ability for perpetual self-renewal and proliferation. They produce downstream progenitor cells and cancer cells that drive tumor growth. Studies of many cancer types including oral squamous cell carcinoma (OSCC) have identified CSCs using specific markers, but it is still unclear as to where in the stem cell hierarchy these markers fall. This is compounded further by the presence of multiple CSC subtypes within OSCC, making investigation reliant on the use of multiple markers. This review paper focuses on the current knowledge in CSC markers including OCT4, SOX2, NANOG, aldehyde dehydrogenase 1, CD44, CD24, CD133 and Musashi-1, highlighting their use and validity in OSCC CSC research. Wolters Kluwer - Medknow 2020 2020-05-08 /pmc/articles/PMC7269290/ /pubmed/32508482 http://dx.doi.org/10.4103/jomfp.JOMFP_336_19 Text en Copyright: © 2020 Journal of Oral and Maxillofacial Pathology http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Review Article
Varun, BR
Jayanthi, P
Ramani, Pratibha
Cancer stem cells: A comprehensive review on identification and therapeutic implications
title Cancer stem cells: A comprehensive review on identification and therapeutic implications
title_full Cancer stem cells: A comprehensive review on identification and therapeutic implications
title_fullStr Cancer stem cells: A comprehensive review on identification and therapeutic implications
title_full_unstemmed Cancer stem cells: A comprehensive review on identification and therapeutic implications
title_short Cancer stem cells: A comprehensive review on identification and therapeutic implications
title_sort cancer stem cells: a comprehensive review on identification and therapeutic implications
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7269290/
https://www.ncbi.nlm.nih.gov/pubmed/32508482
http://dx.doi.org/10.4103/jomfp.JOMFP_336_19
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