Cargando…

Sustained activation of EGFR-ERK1/2 signaling limits the response to tigecycline-induced mitochondrial respiratory deficiency in liver cancer

BACKGROUND: Identification of tumor dependencies is important for developing therapeutic strategies for liver cancer. METHODS: A genome-wide CRISPR screen was performed for finding critical vulnerabilities in liver cancer cells. Compounds screen, RNA sequencing, and human phospho-receptor tyrosine k...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhou, Yangyang, Wang, Siying, Wu, Wei, Ling, Jing, Li, Haoyu, Jia, Qi, Zheng, Jiaojiao, Zheng, Xingling, Yu, Ruobing, Wu, Qiangxin, Shi, Yaoping, Lieftink, Cor, Beijersbergen, Roderick L., Yuan, Shengxian, Bernards, René, Jin, Haojie, Qin, Wenxin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9763382/
https://www.ncbi.nlm.nih.gov/pubmed/36502574
http://dx.doi.org/10.1016/j.ebiom.2022.104397
_version_ 1784853046628450304
author Zhou, Yangyang
Wang, Siying
Wu, Wei
Ling, Jing
Li, Haoyu
Jia, Qi
Zheng, Jiaojiao
Zheng, Xingling
Yu, Ruobing
Wu, Qiangxin
Shi, Yaoping
Lieftink, Cor
Beijersbergen, Roderick L.
Yuan, Shengxian
Bernards, René
Jin, Haojie
Qin, Wenxin
author_facet Zhou, Yangyang
Wang, Siying
Wu, Wei
Ling, Jing
Li, Haoyu
Jia, Qi
Zheng, Jiaojiao
Zheng, Xingling
Yu, Ruobing
Wu, Qiangxin
Shi, Yaoping
Lieftink, Cor
Beijersbergen, Roderick L.
Yuan, Shengxian
Bernards, René
Jin, Haojie
Qin, Wenxin
author_sort Zhou, Yangyang
collection PubMed
description BACKGROUND: Identification of tumor dependencies is important for developing therapeutic strategies for liver cancer. METHODS: A genome-wide CRISPR screen was performed for finding critical vulnerabilities in liver cancer cells. Compounds screen, RNA sequencing, and human phospho-receptor tyrosine kinase arrays were applied to explore mechanisms and search for synergistic drugs. FINDINGS: We identified mitochondrial translation-related genes associated with proliferation for liver cancer cells. Tigecycline induced deficiency of respiratory chain by disturbing mitochondrial translation process and showed therapeutic potential in liver cancer. For liver cancer cells extremely insensitive to tigecycline, a compounds screen was applied to identify MEK inhibitors as synergistic drugs to tigecycline-insensitive liver cancer cells. Mechanistically, sustained activation of EGFR-ERK1/2-MYC cascade conferred the insensitivity to tigecycline, which was mediated by enhanced secretion of EREG and AREG. Moreover, glycolytic enzymes, such as HK2 and PKM2 were upregulated to stimulate glycolysisin a MYC-dependent manner. Tigecycline induced respiratory chain deficiency in combination with cutting off EGFR-ERK1/2-MYC cascade by MEK inhibitors or EGFR inhibitors, resulting in decrease of both oxidative phosphorylation and glycolysis in liver cancer cells. INTERPRETATION: Our study proved that blocking EGFR-ERK1/2-MYC cascade combined with tigecycline could be a potential therapeutic strategy for liver cancer. FUNDING: This work was funded by grants from the 10.13039/501100001809National Natural Science Foundation of China (82073039,82222047, 81920108025), 10.13039/501100012247Program of Shanghai Academic/Technology Research Leader (22XD1423100), Shanghai Municipal Science and Technology Project (20JC1411100), 10.13039/501100013314111 Project (B21024), Innovative Research Team of High-level Local Universities in Shanghai (SHSMU-ZDCX20212700, SHSMU-ZDCX20210802) and Shanghai Jiao Tong University School of Medicine (YG2019GD01).
format Online
Article
Text
id pubmed-9763382
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-97633822022-12-21 Sustained activation of EGFR-ERK1/2 signaling limits the response to tigecycline-induced mitochondrial respiratory deficiency in liver cancer Zhou, Yangyang Wang, Siying Wu, Wei Ling, Jing Li, Haoyu Jia, Qi Zheng, Jiaojiao Zheng, Xingling Yu, Ruobing Wu, Qiangxin Shi, Yaoping Lieftink, Cor Beijersbergen, Roderick L. Yuan, Shengxian Bernards, René Jin, Haojie Qin, Wenxin eBioMedicine Articles BACKGROUND: Identification of tumor dependencies is important for developing therapeutic strategies for liver cancer. METHODS: A genome-wide CRISPR screen was performed for finding critical vulnerabilities in liver cancer cells. Compounds screen, RNA sequencing, and human phospho-receptor tyrosine kinase arrays were applied to explore mechanisms and search for synergistic drugs. FINDINGS: We identified mitochondrial translation-related genes associated with proliferation for liver cancer cells. Tigecycline induced deficiency of respiratory chain by disturbing mitochondrial translation process and showed therapeutic potential in liver cancer. For liver cancer cells extremely insensitive to tigecycline, a compounds screen was applied to identify MEK inhibitors as synergistic drugs to tigecycline-insensitive liver cancer cells. Mechanistically, sustained activation of EGFR-ERK1/2-MYC cascade conferred the insensitivity to tigecycline, which was mediated by enhanced secretion of EREG and AREG. Moreover, glycolytic enzymes, such as HK2 and PKM2 were upregulated to stimulate glycolysisin a MYC-dependent manner. Tigecycline induced respiratory chain deficiency in combination with cutting off EGFR-ERK1/2-MYC cascade by MEK inhibitors or EGFR inhibitors, resulting in decrease of both oxidative phosphorylation and glycolysis in liver cancer cells. INTERPRETATION: Our study proved that blocking EGFR-ERK1/2-MYC cascade combined with tigecycline could be a potential therapeutic strategy for liver cancer. FUNDING: This work was funded by grants from the 10.13039/501100001809National Natural Science Foundation of China (82073039,82222047, 81920108025), 10.13039/501100012247Program of Shanghai Academic/Technology Research Leader (22XD1423100), Shanghai Municipal Science and Technology Project (20JC1411100), 10.13039/501100013314111 Project (B21024), Innovative Research Team of High-level Local Universities in Shanghai (SHSMU-ZDCX20212700, SHSMU-ZDCX20210802) and Shanghai Jiao Tong University School of Medicine (YG2019GD01). Elsevier 2022-12-08 /pmc/articles/PMC9763382/ /pubmed/36502574 http://dx.doi.org/10.1016/j.ebiom.2022.104397 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Articles
Zhou, Yangyang
Wang, Siying
Wu, Wei
Ling, Jing
Li, Haoyu
Jia, Qi
Zheng, Jiaojiao
Zheng, Xingling
Yu, Ruobing
Wu, Qiangxin
Shi, Yaoping
Lieftink, Cor
Beijersbergen, Roderick L.
Yuan, Shengxian
Bernards, René
Jin, Haojie
Qin, Wenxin
Sustained activation of EGFR-ERK1/2 signaling limits the response to tigecycline-induced mitochondrial respiratory deficiency in liver cancer
title Sustained activation of EGFR-ERK1/2 signaling limits the response to tigecycline-induced mitochondrial respiratory deficiency in liver cancer
title_full Sustained activation of EGFR-ERK1/2 signaling limits the response to tigecycline-induced mitochondrial respiratory deficiency in liver cancer
title_fullStr Sustained activation of EGFR-ERK1/2 signaling limits the response to tigecycline-induced mitochondrial respiratory deficiency in liver cancer
title_full_unstemmed Sustained activation of EGFR-ERK1/2 signaling limits the response to tigecycline-induced mitochondrial respiratory deficiency in liver cancer
title_short Sustained activation of EGFR-ERK1/2 signaling limits the response to tigecycline-induced mitochondrial respiratory deficiency in liver cancer
title_sort sustained activation of egfr-erk1/2 signaling limits the response to tigecycline-induced mitochondrial respiratory deficiency in liver cancer
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9763382/
https://www.ncbi.nlm.nih.gov/pubmed/36502574
http://dx.doi.org/10.1016/j.ebiom.2022.104397
work_keys_str_mv AT zhouyangyang sustainedactivationofegfrerk12signalinglimitstheresponsetotigecyclineinducedmitochondrialrespiratorydeficiencyinlivercancer
AT wangsiying sustainedactivationofegfrerk12signalinglimitstheresponsetotigecyclineinducedmitochondrialrespiratorydeficiencyinlivercancer
AT wuwei sustainedactivationofegfrerk12signalinglimitstheresponsetotigecyclineinducedmitochondrialrespiratorydeficiencyinlivercancer
AT lingjing sustainedactivationofegfrerk12signalinglimitstheresponsetotigecyclineinducedmitochondrialrespiratorydeficiencyinlivercancer
AT lihaoyu sustainedactivationofegfrerk12signalinglimitstheresponsetotigecyclineinducedmitochondrialrespiratorydeficiencyinlivercancer
AT jiaqi sustainedactivationofegfrerk12signalinglimitstheresponsetotigecyclineinducedmitochondrialrespiratorydeficiencyinlivercancer
AT zhengjiaojiao sustainedactivationofegfrerk12signalinglimitstheresponsetotigecyclineinducedmitochondrialrespiratorydeficiencyinlivercancer
AT zhengxingling sustainedactivationofegfrerk12signalinglimitstheresponsetotigecyclineinducedmitochondrialrespiratorydeficiencyinlivercancer
AT yuruobing sustainedactivationofegfrerk12signalinglimitstheresponsetotigecyclineinducedmitochondrialrespiratorydeficiencyinlivercancer
AT wuqiangxin sustainedactivationofegfrerk12signalinglimitstheresponsetotigecyclineinducedmitochondrialrespiratorydeficiencyinlivercancer
AT shiyaoping sustainedactivationofegfrerk12signalinglimitstheresponsetotigecyclineinducedmitochondrialrespiratorydeficiencyinlivercancer
AT lieftinkcor sustainedactivationofegfrerk12signalinglimitstheresponsetotigecyclineinducedmitochondrialrespiratorydeficiencyinlivercancer
AT beijersbergenroderickl sustainedactivationofegfrerk12signalinglimitstheresponsetotigecyclineinducedmitochondrialrespiratorydeficiencyinlivercancer
AT yuanshengxian sustainedactivationofegfrerk12signalinglimitstheresponsetotigecyclineinducedmitochondrialrespiratorydeficiencyinlivercancer
AT bernardsrene sustainedactivationofegfrerk12signalinglimitstheresponsetotigecyclineinducedmitochondrialrespiratorydeficiencyinlivercancer
AT jinhaojie sustainedactivationofegfrerk12signalinglimitstheresponsetotigecyclineinducedmitochondrialrespiratorydeficiencyinlivercancer
AT qinwenxin sustainedactivationofegfrerk12signalinglimitstheresponsetotigecyclineinducedmitochondrialrespiratorydeficiencyinlivercancer