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FOXO transcription factors at the interface of metabolism and cancer

Wolfgang Link

Corresponding Author

E-mail address: walink@ualg.pt

Centre for Biomedical Research (CBMR), University of Algarve, Campus of Gambelas, Building 8, room 2.22, Faro, 8005‐139 Portugal

Regenerative Medicine Program, Department of Biomedical Sciences and Medicine, University of Algarve, Campus de Gambelas, Faro, 8005‐139 Portugal

Algarve Biomedical Center (ABC), University of Algarve, Campus de Gambelas, Faro, 8005‐139 Portugal

Correspondence to: Wolfgang Link, University of Algarve, Portugal, E‐mail:

walink@ualg.pt

or Pablo J. Fernandez‐Marcos, IMDEA Food, Spain, E‐mail:

pablojose.fernandez@imdea.org

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Pablo J. Fernandez‐Marcos

Corresponding Author

E-mail address: pablojose.fernandez@imdea.org

Madrid Institute for Advanced Studies – IMDEA Food, CEI UAM + CSIC, Madrid, E28049 Spain

Correspondence to: Wolfgang Link, University of Algarve, Portugal, E‐mail:

walink@ualg.pt

or Pablo J. Fernandez‐Marcos, IMDEA Food, Spain, E‐mail:

pablojose.fernandez@imdea.org

Search for more papers by this author
First published: 19 June 2017
Cited by: 9

Abstract

Diabetes refers to a group of metabolic diseases characterized by impaired insulin signalling and high blood glucose. A growing body of epidemiological evidence links diabetes to several types of cancer but the underlying molecular mechanisms are poorly understood. The signalling cascade connecting insulin and FOXO proteins provides a compelling example for a conserved pathway at the interface between insulin signalling and cancer. FOXOs are transcription factors that orchestrate programs of gene expression known to control a variety of processes in response to cellular stress. Genes regulated by this family of proteins are involved in the regulation of cellular energy production, oxidative stress resistance and cell viability and proliferation. Accordingly, FOXO factors have been shown to play an important role in the suppression of tumour growth and in the regulation of metabolic homeostasis. There is emerging evidence that deregulation of FOXO factors might account for the association between insulin resistance‐related metabolic disorders and cancer.

Number of times cited according to CrossRef: 9

  • , Image-based Identification of Chemical Compounds Capable of Trapping FOXO in the Cell Nucleus, FOXO Transcription Factors, 10.1007/978-1-4939-8900-3_14, (163-170), (2018).
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  • , FOXO3a-dependent up-regulation of Mxi1-0 promotes hypoxia-induced apoptosis in endothelial cells, Cellular Signalling, 10.1016/j.cellsig.2018.08.009, 51, (233-242), (2018).
  • , Forkhead box O proteins: Crucial regulators of cancer EMT, Seminars in Cancer Biology, 10.1016/j.semcancer.2018.02.004, (2018).
  • , The regulation of FOXO1 and its role in disease progression, Life Sciences, 10.1016/j.lfs.2017.11.030, 193, (124-131), (2018).
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  • , Thyrotroph embryonic factor is downregulated in bladder cancer and suppresses proliferation and tumorigenesis via the AKT/FOXOs signalling pathway, Cell Proliferation, e12560, (2018).