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NFATc2 enhances tumor-initiating phenotypes through the NFATc2/SOX2/ALDH axis in lung adenocarcinoma
Tumor-initiating cells (TIC) are dynamic cancer cell subsets that display enhanced tumor functions and resilience to treatment but the mechanism of TIC induction or maintenance in lung cancer is not fully understood. In this study, we show the calcium pathway transcription factor NFATc2 is a novel r...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5570574/ https://www.ncbi.nlm.nih.gov/pubmed/28737489 http://dx.doi.org/10.7554/eLife.26733 |
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author | Xiao, Zhi-Jie Liu, Jing Wang, Si-Qi Zhu, Yun Gao, Xu-Yuan Tin, Vicky Pui-Chi Qin, Jing Wang, Jun-Wen Wong, Maria Pik |
author_facet | Xiao, Zhi-Jie Liu, Jing Wang, Si-Qi Zhu, Yun Gao, Xu-Yuan Tin, Vicky Pui-Chi Qin, Jing Wang, Jun-Wen Wong, Maria Pik |
author_sort | Xiao, Zhi-Jie |
collection | PubMed |
description | Tumor-initiating cells (TIC) are dynamic cancer cell subsets that display enhanced tumor functions and resilience to treatment but the mechanism of TIC induction or maintenance in lung cancer is not fully understood. In this study, we show the calcium pathway transcription factor NFATc2 is a novel regulator of lung TIC phenotypes, including tumorspheres, cell motility, tumorigenesis, as well as in vitro and in vivo responses to chemotherapy and targeted therapy. In human lung cancers, high NFATc2 expression predicted poor tumor differentiation, adverse recurrence-free and cancer-specific overall survivals. Mechanistic investigations identified NFATc2 response elements in the 3’ enhancer region of SOX2, and NFATc2/SOX2 coupling upregulates ALDH1A1 by binding to its 5’ enhancer. Through this axis, oxidative stress induced by cancer drug treatment is attenuated, leading to increased resistance in a mutation-independent manner. Targeting this axis provides a novel approach for the long-term treatment of lung cancer through TIC elimination. DOI: http://dx.doi.org/10.7554/eLife.26733.001 |
format | Online Article Text |
id | pubmed-5570574 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-55705742017-08-28 NFATc2 enhances tumor-initiating phenotypes through the NFATc2/SOX2/ALDH axis in lung adenocarcinoma Xiao, Zhi-Jie Liu, Jing Wang, Si-Qi Zhu, Yun Gao, Xu-Yuan Tin, Vicky Pui-Chi Qin, Jing Wang, Jun-Wen Wong, Maria Pik eLife Cancer Biology Tumor-initiating cells (TIC) are dynamic cancer cell subsets that display enhanced tumor functions and resilience to treatment but the mechanism of TIC induction or maintenance in lung cancer is not fully understood. In this study, we show the calcium pathway transcription factor NFATc2 is a novel regulator of lung TIC phenotypes, including tumorspheres, cell motility, tumorigenesis, as well as in vitro and in vivo responses to chemotherapy and targeted therapy. In human lung cancers, high NFATc2 expression predicted poor tumor differentiation, adverse recurrence-free and cancer-specific overall survivals. Mechanistic investigations identified NFATc2 response elements in the 3’ enhancer region of SOX2, and NFATc2/SOX2 coupling upregulates ALDH1A1 by binding to its 5’ enhancer. Through this axis, oxidative stress induced by cancer drug treatment is attenuated, leading to increased resistance in a mutation-independent manner. Targeting this axis provides a novel approach for the long-term treatment of lung cancer through TIC elimination. DOI: http://dx.doi.org/10.7554/eLife.26733.001 eLife Sciences Publications, Ltd 2017-07-24 /pmc/articles/PMC5570574/ /pubmed/28737489 http://dx.doi.org/10.7554/eLife.26733 Text en © 2017, Xiao et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cancer Biology Xiao, Zhi-Jie Liu, Jing Wang, Si-Qi Zhu, Yun Gao, Xu-Yuan Tin, Vicky Pui-Chi Qin, Jing Wang, Jun-Wen Wong, Maria Pik NFATc2 enhances tumor-initiating phenotypes through the NFATc2/SOX2/ALDH axis in lung adenocarcinoma |
title | NFATc2 enhances tumor-initiating phenotypes through the NFATc2/SOX2/ALDH axis in lung adenocarcinoma |
title_full | NFATc2 enhances tumor-initiating phenotypes through the NFATc2/SOX2/ALDH axis in lung adenocarcinoma |
title_fullStr | NFATc2 enhances tumor-initiating phenotypes through the NFATc2/SOX2/ALDH axis in lung adenocarcinoma |
title_full_unstemmed | NFATc2 enhances tumor-initiating phenotypes through the NFATc2/SOX2/ALDH axis in lung adenocarcinoma |
title_short | NFATc2 enhances tumor-initiating phenotypes through the NFATc2/SOX2/ALDH axis in lung adenocarcinoma |
title_sort | nfatc2 enhances tumor-initiating phenotypes through the nfatc2/sox2/aldh axis in lung adenocarcinoma |
topic | Cancer Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5570574/ https://www.ncbi.nlm.nih.gov/pubmed/28737489 http://dx.doi.org/10.7554/eLife.26733 |
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