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Mucosal ribosomal stress-induced PRDM1 promotes chemoresistance via stemness regulation

The majorities of colorectal cancer (CRC) cases are sporadic in origin and a large proportion of etiologies are associated with environmental stress responses. In response to external and internal stress, the ribosome stands sentinel and stress-driven ribosomal dysfunction triggers the cellular deci...

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Autores principales: Kim, Juil, Moon, Yuseok
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8110964/
https://www.ncbi.nlm.nih.gov/pubmed/33972671
http://dx.doi.org/10.1038/s42003-021-02078-1
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author Kim, Juil
Moon, Yuseok
author_facet Kim, Juil
Moon, Yuseok
author_sort Kim, Juil
collection PubMed
description The majorities of colorectal cancer (CRC) cases are sporadic in origin and a large proportion of etiologies are associated with environmental stress responses. In response to external and internal stress, the ribosome stands sentinel and stress-driven ribosomal dysfunction triggers the cellular decision pathways via transcriptional reprogramming. In the present study, PR domain zinc finger protein (PRDM) 1, a master transcriptional regulator, was found to be closely associated with ribosomal actions in patients with CRC and the murine models. Stress-driven ribosomal dysfunction enhanced PRDM1 levels in intestinal cancer cells, which contributed to their survival and enhanced cancer cell stemness against cancer treatment. Mechanistically, PRDM1 facilitated clustering modulation of insulin-like growth factor (IGF) receptor-associated genes, which supported cancer cell growth and stemness-linked features. Ribosomal dysfunction-responsive PRDM1 facilitated signaling remodeling for the survival of tumor progenitors, providing compelling evidence for the progression of sporadic CRC.
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spelling pubmed-81109642021-05-12 Mucosal ribosomal stress-induced PRDM1 promotes chemoresistance via stemness regulation Kim, Juil Moon, Yuseok Commun Biol Article The majorities of colorectal cancer (CRC) cases are sporadic in origin and a large proportion of etiologies are associated with environmental stress responses. In response to external and internal stress, the ribosome stands sentinel and stress-driven ribosomal dysfunction triggers the cellular decision pathways via transcriptional reprogramming. In the present study, PR domain zinc finger protein (PRDM) 1, a master transcriptional regulator, was found to be closely associated with ribosomal actions in patients with CRC and the murine models. Stress-driven ribosomal dysfunction enhanced PRDM1 levels in intestinal cancer cells, which contributed to their survival and enhanced cancer cell stemness against cancer treatment. Mechanistically, PRDM1 facilitated clustering modulation of insulin-like growth factor (IGF) receptor-associated genes, which supported cancer cell growth and stemness-linked features. Ribosomal dysfunction-responsive PRDM1 facilitated signaling remodeling for the survival of tumor progenitors, providing compelling evidence for the progression of sporadic CRC. Nature Publishing Group UK 2021-05-10 /pmc/articles/PMC8110964/ /pubmed/33972671 http://dx.doi.org/10.1038/s42003-021-02078-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Kim, Juil
Moon, Yuseok
Mucosal ribosomal stress-induced PRDM1 promotes chemoresistance via stemness regulation
title Mucosal ribosomal stress-induced PRDM1 promotes chemoresistance via stemness regulation
title_full Mucosal ribosomal stress-induced PRDM1 promotes chemoresistance via stemness regulation
title_fullStr Mucosal ribosomal stress-induced PRDM1 promotes chemoresistance via stemness regulation
title_full_unstemmed Mucosal ribosomal stress-induced PRDM1 promotes chemoresistance via stemness regulation
title_short Mucosal ribosomal stress-induced PRDM1 promotes chemoresistance via stemness regulation
title_sort mucosal ribosomal stress-induced prdm1 promotes chemoresistance via stemness regulation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8110964/
https://www.ncbi.nlm.nih.gov/pubmed/33972671
http://dx.doi.org/10.1038/s42003-021-02078-1
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