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mTOR inhibition attenuates chemosensitivity through the induction of chemotherapy resistant persisters

Chemotherapy can eradicate a majority of cancer cells. However, a small population of tumor cells often survives drug treatments through genetic and/or non-genetic mechanisms, leading to tumor recurrence. Here we report a reversible chemoresistance phenotype regulated by the mTOR pathway. Through a...

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Autores principales: Liu, Yuanhui, Azizian, Nancy G., Sullivan, Delaney K., Li, Yulin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9671908/
https://www.ncbi.nlm.nih.gov/pubmed/36396656
http://dx.doi.org/10.1038/s41467-022-34890-6
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author Liu, Yuanhui
Azizian, Nancy G.
Sullivan, Delaney K.
Li, Yulin
author_facet Liu, Yuanhui
Azizian, Nancy G.
Sullivan, Delaney K.
Li, Yulin
author_sort Liu, Yuanhui
collection PubMed
description Chemotherapy can eradicate a majority of cancer cells. However, a small population of tumor cells often survives drug treatments through genetic and/or non-genetic mechanisms, leading to tumor recurrence. Here we report a reversible chemoresistance phenotype regulated by the mTOR pathway. Through a genome-wide CRISPR knockout library screen in pancreatic cancer cells treated with chemotherapeutic agents, we have identified the mTOR pathway as a prominent determinant of chemosensitivity. Pharmacological suppression of mTOR activity in cancer cells from diverse tissue origins leads to the persistence of a reversibly resistant population, which is otherwise eliminated by chemotherapeutic agents. Conversely, activation of the mTOR pathway increases chemosensitivity in vitro and in vivo and predicts better survival among various human cancers. Persister cells display a senescence phenotype. Inhibition of mTOR does not induce cellular senescence per se, but rather promotes the survival of senescent cells through regulation of autophagy and G2/M cell cycle arrest, as revealed by a small-molecule chemical library screen. Thus, mTOR plays a causal yet paradoxical role in regulating chemotherapeutic response; inhibition of the mTOR pathway, while suppressing tumor expansion, facilitates the development of a reversible drug-tolerant senescence state.
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spelling pubmed-96719082022-11-19 mTOR inhibition attenuates chemosensitivity through the induction of chemotherapy resistant persisters Liu, Yuanhui Azizian, Nancy G. Sullivan, Delaney K. Li, Yulin Nat Commun Article Chemotherapy can eradicate a majority of cancer cells. However, a small population of tumor cells often survives drug treatments through genetic and/or non-genetic mechanisms, leading to tumor recurrence. Here we report a reversible chemoresistance phenotype regulated by the mTOR pathway. Through a genome-wide CRISPR knockout library screen in pancreatic cancer cells treated with chemotherapeutic agents, we have identified the mTOR pathway as a prominent determinant of chemosensitivity. Pharmacological suppression of mTOR activity in cancer cells from diverse tissue origins leads to the persistence of a reversibly resistant population, which is otherwise eliminated by chemotherapeutic agents. Conversely, activation of the mTOR pathway increases chemosensitivity in vitro and in vivo and predicts better survival among various human cancers. Persister cells display a senescence phenotype. Inhibition of mTOR does not induce cellular senescence per se, but rather promotes the survival of senescent cells through regulation of autophagy and G2/M cell cycle arrest, as revealed by a small-molecule chemical library screen. Thus, mTOR plays a causal yet paradoxical role in regulating chemotherapeutic response; inhibition of the mTOR pathway, while suppressing tumor expansion, facilitates the development of a reversible drug-tolerant senescence state. Nature Publishing Group UK 2022-11-17 /pmc/articles/PMC9671908/ /pubmed/36396656 http://dx.doi.org/10.1038/s41467-022-34890-6 Text en © The Author(s) 2022 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
Liu, Yuanhui
Azizian, Nancy G.
Sullivan, Delaney K.
Li, Yulin
mTOR inhibition attenuates chemosensitivity through the induction of chemotherapy resistant persisters
title mTOR inhibition attenuates chemosensitivity through the induction of chemotherapy resistant persisters
title_full mTOR inhibition attenuates chemosensitivity through the induction of chemotherapy resistant persisters
title_fullStr mTOR inhibition attenuates chemosensitivity through the induction of chemotherapy resistant persisters
title_full_unstemmed mTOR inhibition attenuates chemosensitivity through the induction of chemotherapy resistant persisters
title_short mTOR inhibition attenuates chemosensitivity through the induction of chemotherapy resistant persisters
title_sort mtor inhibition attenuates chemosensitivity through the induction of chemotherapy resistant persisters
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9671908/
https://www.ncbi.nlm.nih.gov/pubmed/36396656
http://dx.doi.org/10.1038/s41467-022-34890-6
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