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Transcriptional census of epithelial-mesenchymal plasticity in cancer

Epithelial-mesenchymal plasticity (EMP) contributes to tumor progression, promoting therapy resistance and immune cell evasion. Definitive molecular features of this plasticity have largely remained elusive due to the limited scale of most studies. Leveraging single-cell RNA sequencing data from 266...

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Detalles Bibliográficos
Autores principales: Cook, David P., Vanderhyden, Barbara C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8730603/
https://www.ncbi.nlm.nih.gov/pubmed/34985957
http://dx.doi.org/10.1126/sciadv.abi7640
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author Cook, David P.
Vanderhyden, Barbara C.
author_facet Cook, David P.
Vanderhyden, Barbara C.
author_sort Cook, David P.
collection PubMed
description Epithelial-mesenchymal plasticity (EMP) contributes to tumor progression, promoting therapy resistance and immune cell evasion. Definitive molecular features of this plasticity have largely remained elusive due to the limited scale of most studies. Leveraging single-cell RNA sequencing data from 266 tumors spanning eight different cancer types, we identify expression patterns associated with intratumoral EMP. Integrative analysis of these programs confirmed a high degree of diversity among tumors. These diverse programs are associated with combinations of various common regulatory mechanisms initiated from cues within the tumor microenvironment. We show that inferring regulatory features can inform effective therapeutics to restrict EMP.
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spelling pubmed-87306032022-01-19 Transcriptional census of epithelial-mesenchymal plasticity in cancer Cook, David P. Vanderhyden, Barbara C. Sci Adv Biomedicine and Life Sciences Epithelial-mesenchymal plasticity (EMP) contributes to tumor progression, promoting therapy resistance and immune cell evasion. Definitive molecular features of this plasticity have largely remained elusive due to the limited scale of most studies. Leveraging single-cell RNA sequencing data from 266 tumors spanning eight different cancer types, we identify expression patterns associated with intratumoral EMP. Integrative analysis of these programs confirmed a high degree of diversity among tumors. These diverse programs are associated with combinations of various common regulatory mechanisms initiated from cues within the tumor microenvironment. We show that inferring regulatory features can inform effective therapeutics to restrict EMP. American Association for the Advancement of Science 2022-01-05 /pmc/articles/PMC8730603/ /pubmed/34985957 http://dx.doi.org/10.1126/sciadv.abi7640 Text en Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Biomedicine and Life Sciences
Cook, David P.
Vanderhyden, Barbara C.
Transcriptional census of epithelial-mesenchymal plasticity in cancer
title Transcriptional census of epithelial-mesenchymal plasticity in cancer
title_full Transcriptional census of epithelial-mesenchymal plasticity in cancer
title_fullStr Transcriptional census of epithelial-mesenchymal plasticity in cancer
title_full_unstemmed Transcriptional census of epithelial-mesenchymal plasticity in cancer
title_short Transcriptional census of epithelial-mesenchymal plasticity in cancer
title_sort transcriptional census of epithelial-mesenchymal plasticity in cancer
topic Biomedicine and Life Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8730603/
https://www.ncbi.nlm.nih.gov/pubmed/34985957
http://dx.doi.org/10.1126/sciadv.abi7640
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