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Zinc finger E-box-binding homeobox 1 mediates aerobic glycolysis via suppression of sirtuin 3 in pancreatic cancer.


ABSTRACT: AIM:To uncover the roles of tumor-promoting gene ZEB1 in aerobic glycolysis regulation and shed light on the underlying molecular mechanism. METHODS:Endogenous zinc finger E-box binding homeobox-1 (ZEB1) was silenced using a lentivirus-mediated method, and the impact of ZEB1 and methyl-CpG binding domain protein 1 (MBD1) on aerobic glycolysis was measured using seahorse cellular flux analyzers, reactive oxygen species quantification, and mitochondrial membrane potential measurement. The interaction between ZEB1 and MBD1 was assessed by co-immunoprecipitation and immunofluorescence assays. The impact of ZEB1 and MBD1 interaction on sirtuin 3 (SIRT3) expression was confirmed by quantitative polymerase chain reaction, western blotting, and dual-luciferase and chromatin-immunoprecipitation assays. RESULTS:ZEB1 was a positive regulator of aerobic glycolysis in pancreatic cancer. ZEB1 transcriptionally silenced expression of SIRT3, a mitochondrial-localized tumor suppressor, through interaction with MBD1. CONCLUSION:ZEB1 silenced SIRT3 expression via interaction with MBD1 to promote aerobic glycolysis in pancreatic cancer.

SUBMITTER: Xu WY 

PROVIDER: S-EPMC6250915 | biostudies-other | 2018 Nov

REPOSITORIES: biostudies-other

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Zinc finger E-box-binding homeobox 1 mediates aerobic glycolysis <i>via</i> suppression of sirtuin 3 in pancreatic cancer.

Xu Wen-Yan WY   Hu Qiang-Sheng QS   Qin Yi Y   Zhang Bo B   Liu Wen-Sheng WS   Ni Quan-Xing QX   Xu Jin J   Yu Xian-Jun XJ  

World journal of gastroenterology 20181101 43


<h4>Aim</h4>To uncover the roles of tumor-promoting gene <i>ZEB1</i> in aerobic glycolysis regulation and shed light on the underlying molecular mechanism.<h4>Methods</h4>Endogenous zinc finger E-box binding homeobox-1 (ZEB1) was silenced using a lentivirus-mediated method, and the impact of ZEB1 and methyl-CpG binding domain protein 1 (MBD1) on aerobic glycolysis was measured using seahorse cellular flux analyzers, reactive oxygen species quantification, and mitochondrial membrane potential mea  ...[more]

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