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FEBS J. 2017 Oct;284(19):3132-3144. doi: 10.1111/febs.14090. Epub 2017 May 21.

Metabolic reprogramming and epithelial-to-mesenchymal transition in cancer.

Author information

1
Medical Research Council Cancer Unit, Hutchison/MRC Research Centre, University of Cambridge, UK.

Abstract

Several lines of evidence indicate that during transformation epithelial cancer cells can acquire mesenchymal features via a process called epithelial-to-mesenchymal transition (EMT). This process endows cancer cells with increased invasive and migratory capacity, enabling tumour dissemination and metastasis. EMT is associated with a complex metabolic reprogramming, orchestrated by EMT transcription factors, which support the energy requirements of increased motility and growth in harsh environmental conditions. The discovery that mutations in metabolic genes such as FH, SDH and IDH activate EMT provided further evidence that EMT and metabolism are intertwined. In this review, we discuss the role of EMT in cancer and the underpinning metabolic reprogramming. We also put forward the hypothesis that, by altering chromatin structure and function, metabolic pathways engaged by EMT are necessary for its full activation.

KEYWORDS:

EMT; FH; IDH; SDH; cancer; epigenetics; metabolism; metastasis; mitochondrial metabolism

PMID:
28444969
PMCID:
PMC6049610
DOI:
10.1111/febs.14090
[Indexed for MEDLINE]
Free PMC Article

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