Literature DB >> 28444969

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

Marco Sciacovelli1, Christian Frezza1.   

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.
© 2017 Federation of European Biochemical Societies.

Entities:  

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

Mesh:

Substances:

Year:  2017        PMID: 28444969      PMCID: PMC6049610          DOI: 10.1111/febs.14090

Source DB:  PubMed          Journal:  FEBS J        ISSN: 1742-464X            Impact factor:   5.542


  100 in total

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7.  Glutaminolysis is a metabolic route essential for survival and growth of prostate cancer cells and a target of 5α-dihydrotestosterone regulation.

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