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Ras Downstream Effector GGCT Alleviates Oncogenic Stress

How cells adapt to oncogenic transformation-associated cellular stress and become fully transformed is still unknown. Here we identified a novel GGCT-regulated glutathione (GSH)-reactive oxygen species (ROS) metabolic pathway in oncogenic stress alleviation. We identified GGCT as a target of oncogen...

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Detalles Bibliográficos
Autores principales: He, Zaoke, Wang, Shixiang, Shao, Yuanyuan, Zhang, Jing, Wu, Xiaolin, Chen, Yuxing, Hu, Junhao, Zhang, Feng, Liu, Xue-Song
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6700472/
https://www.ncbi.nlm.nih.gov/pubmed/31400748
http://dx.doi.org/10.1016/j.isci.2019.07.036
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author He, Zaoke
Wang, Shixiang
Shao, Yuanyuan
Zhang, Jing
Wu, Xiaolin
Chen, Yuxing
Hu, Junhao
Zhang, Feng
Liu, Xue-Song
author_facet He, Zaoke
Wang, Shixiang
Shao, Yuanyuan
Zhang, Jing
Wu, Xiaolin
Chen, Yuxing
Hu, Junhao
Zhang, Feng
Liu, Xue-Song
author_sort He, Zaoke
collection PubMed
description How cells adapt to oncogenic transformation-associated cellular stress and become fully transformed is still unknown. Here we identified a novel GGCT-regulated glutathione (GSH)-reactive oxygen species (ROS) metabolic pathway in oncogenic stress alleviation. We identified GGCT as a target of oncogenic Ras and that it is required for oncogenic Ras-induced primary mouse cell proliferation and transformation and in vivo lung cancer formation in the LSL-Kras G12D mouse model. However, GGCT deficiency is compatible with normal mouse development, suggesting that GGCT can be a cancer-specific therapeutic target. Genetically amplified GGCT locus further supports the oncogenic driving function of GGCT. In summary, our study not only identifies an oncogenic function of GGCT but also identifies a novel regulator of GSH metabolism, with implications for further understanding of oncogenic stress and cancer treatment.
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spelling pubmed-67004722019-08-26 Ras Downstream Effector GGCT Alleviates Oncogenic Stress He, Zaoke Wang, Shixiang Shao, Yuanyuan Zhang, Jing Wu, Xiaolin Chen, Yuxing Hu, Junhao Zhang, Feng Liu, Xue-Song iScience Article How cells adapt to oncogenic transformation-associated cellular stress and become fully transformed is still unknown. Here we identified a novel GGCT-regulated glutathione (GSH)-reactive oxygen species (ROS) metabolic pathway in oncogenic stress alleviation. We identified GGCT as a target of oncogenic Ras and that it is required for oncogenic Ras-induced primary mouse cell proliferation and transformation and in vivo lung cancer formation in the LSL-Kras G12D mouse model. However, GGCT deficiency is compatible with normal mouse development, suggesting that GGCT can be a cancer-specific therapeutic target. Genetically amplified GGCT locus further supports the oncogenic driving function of GGCT. In summary, our study not only identifies an oncogenic function of GGCT but also identifies a novel regulator of GSH metabolism, with implications for further understanding of oncogenic stress and cancer treatment. Elsevier 2019-07-26 /pmc/articles/PMC6700472/ /pubmed/31400748 http://dx.doi.org/10.1016/j.isci.2019.07.036 Text en © 2019 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
He, Zaoke
Wang, Shixiang
Shao, Yuanyuan
Zhang, Jing
Wu, Xiaolin
Chen, Yuxing
Hu, Junhao
Zhang, Feng
Liu, Xue-Song
Ras Downstream Effector GGCT Alleviates Oncogenic Stress
title Ras Downstream Effector GGCT Alleviates Oncogenic Stress
title_full Ras Downstream Effector GGCT Alleviates Oncogenic Stress
title_fullStr Ras Downstream Effector GGCT Alleviates Oncogenic Stress
title_full_unstemmed Ras Downstream Effector GGCT Alleviates Oncogenic Stress
title_short Ras Downstream Effector GGCT Alleviates Oncogenic Stress
title_sort ras downstream effector ggct alleviates oncogenic stress
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6700472/
https://www.ncbi.nlm.nih.gov/pubmed/31400748
http://dx.doi.org/10.1016/j.isci.2019.07.036
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