Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/89157
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dc.contributor.authorTeo, Ziqiangen
dc.contributor.authorSng, Ming Keaten
dc.contributor.authorChan, Jeremy Soon Kiaten
dc.contributor.authorLim, Maegan Miang Keeen
dc.contributor.authorLi, Yinliangen
dc.contributor.authorLi, Luchunen
dc.contributor.authorPhua, Terrien
dc.contributor.authorLee, J. Y. H.en
dc.contributor.authorTan, Zhen Weien
dc.contributor.authorZhu, Pengchengen
dc.contributor.authorTan, Nguan Soonen
dc.date.accessioned2018-05-18T08:13:17Zen
dc.date.accessioned2019-12-06T17:19:09Z-
dc.date.available2018-05-18T08:13:17Zen
dc.date.available2019-12-06T17:19:09Z-
dc.date.issued2017en
dc.identifier.citationTeo, Z., Sng, M. K., Chan, J. S. K., Lim, M. M. K., Li, Y., Li, L., et al. (2017). Elevation of adenylate energy charge by angiopoietin-like 4 enhances epithelial–mesenchymal transition by inducing 14-3-3γ expression. Oncogene, 36(46), 6408-6419.en
dc.identifier.issn0950-9232en
dc.identifier.urihttps://hdl.handle.net/10356/89157-
dc.description.abstractMetastatic cancer cells acquire energy-intensive processes including increased invasiveness and chemoresistance. However, how the energy demand is met and the molecular drivers that coordinate an increase in cellular metabolic activity to drive epithelial–mesenchymal transition (EMT), the first step of metastasis, remain unclear. Using different in vitro and in vivo EMT models with clinical patient’s samples, we showed that EMT is an energy-demanding process fueled by glucose metabolism-derived adenosine triphosphate (ATP). We identified angiopoietin-like 4 (ANGPTL4) as a key player that coordinates an increase in cellular energy flux crucial for EMT via an ANGPTL4/14-3-3γ signaling axis. This augmented cellular metabolic activity enhanced metastasis. ANGPTL4 knockdown suppresses an adenylate energy charge elevation, delaying EMT. Using an in vivo dual-inducible EMT model, we found that ANGPTL4 deficiency reduces cancer metastasis to the lung and liver. Unbiased kinase inhibitor screens and Ingenuity Pathway Analysis revealed that ANGPTL4 regulates the expression of 14-3-3γ adaptor protein via the phosphatidylinositol-3-kinase/AKT and mitogen-activated protein kinase signaling pathways that culminate to activation of transcription factors, CREB, cFOS and STAT3. Using a different mode of action, as compared with protein kinases, the ANGPTL4/14-3-3γ signaling axis consolidated cellular bioenergetics and stabilized critical EMT proteins to coordinate energy demand and enhanced EMT competency and metastasis, through interaction with specific phosphorylation signals on target proteins.en
dc.description.sponsorshipMOE (Min. of Education, S’pore)en
dc.format.extent12 p.en
dc.language.isoenen
dc.relation.ispartofseriesOncogeneen
dc.rights© 2017 The Author(s) (Nature Publishing Group). This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/en
dc.subjectCanceren
dc.subjectCell Biologyen
dc.titleElevation of adenylate energy charge by angiopoietin-like 4 enhances epithelial–mesenchymal transition by inducing 14-3-3γ expressionen
dc.typeJournal Articleen
dc.contributor.schoolLee Kong Chian School of Medicine (LKCMedicine)en
dc.contributor.schoolSchool of Biological Sciencesen
dc.identifier.doi10.1038/onc.2017.244en
dc.description.versionPublished versionen
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item.grantfulltextopen-
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