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Engaging plasticity: Differentiation therapy in solid tumors

Cancer is a systemic heterogeneous disease that can undergo several rounds of latency and activation. Tumor progression evolves by increasing diversity, adaptation to signals from the microenvironment and escape mechanisms from therapy. These dynamic processes indicate necessity for cell plasticity....

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Detalles Bibliográficos
Autores principales: Bar-Hai, Neta, Ishay-Ronen, Dana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9410762/
https://www.ncbi.nlm.nih.gov/pubmed/36034865
http://dx.doi.org/10.3389/fphar.2022.944773
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author Bar-Hai, Neta
Ishay-Ronen, Dana
author_facet Bar-Hai, Neta
Ishay-Ronen, Dana
author_sort Bar-Hai, Neta
collection PubMed
description Cancer is a systemic heterogeneous disease that can undergo several rounds of latency and activation. Tumor progression evolves by increasing diversity, adaptation to signals from the microenvironment and escape mechanisms from therapy. These dynamic processes indicate necessity for cell plasticity. Epithelial-mesenchymal transition (EMT) plays a major role in facilitating cell plasticity in solid tumors by inducing dedifferentiation and cell type transitions. These two practices, plasticity and dedifferentiation enhance tumor heterogeneity creating a key challenge in cancer treatment. In this review we will explore cancer cell plasticity and elaborate treatment modalities that aspire to overcome such dynamic processes in solid tumors. We will further discuss the therapeutic potential of utilizing enhanced cell plasticity for differentiation therapy.
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spelling pubmed-94107622022-08-26 Engaging plasticity: Differentiation therapy in solid tumors Bar-Hai, Neta Ishay-Ronen, Dana Front Pharmacol Pharmacology Cancer is a systemic heterogeneous disease that can undergo several rounds of latency and activation. Tumor progression evolves by increasing diversity, adaptation to signals from the microenvironment and escape mechanisms from therapy. These dynamic processes indicate necessity for cell plasticity. Epithelial-mesenchymal transition (EMT) plays a major role in facilitating cell plasticity in solid tumors by inducing dedifferentiation and cell type transitions. These two practices, plasticity and dedifferentiation enhance tumor heterogeneity creating a key challenge in cancer treatment. In this review we will explore cancer cell plasticity and elaborate treatment modalities that aspire to overcome such dynamic processes in solid tumors. We will further discuss the therapeutic potential of utilizing enhanced cell plasticity for differentiation therapy. Frontiers Media S.A. 2022-08-11 /pmc/articles/PMC9410762/ /pubmed/36034865 http://dx.doi.org/10.3389/fphar.2022.944773 Text en Copyright © 2022 Bar-Hai and Ishay-Ronen. https://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
Bar-Hai, Neta
Ishay-Ronen, Dana
Engaging plasticity: Differentiation therapy in solid tumors
title Engaging plasticity: Differentiation therapy in solid tumors
title_full Engaging plasticity: Differentiation therapy in solid tumors
title_fullStr Engaging plasticity: Differentiation therapy in solid tumors
title_full_unstemmed Engaging plasticity: Differentiation therapy in solid tumors
title_short Engaging plasticity: Differentiation therapy in solid tumors
title_sort engaging plasticity: differentiation therapy in solid tumors
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9410762/
https://www.ncbi.nlm.nih.gov/pubmed/36034865
http://dx.doi.org/10.3389/fphar.2022.944773
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