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The dual specificity role of transcription factor FOXO in type 2-diabetes and cancer

  • Kaneez Fatima
  • , Shilu Mathew
  • , Muhammed Faheem
  • , Tahir Mehmood
  • , Hadi Mohamad Yassine
  • , Asmaa A. Al Thani
  • , Hany Abdel-Hafiz
  • , Khalid Al Ghamdy
  • , Ishtiaq Qadri

Research output: Contribution to journal › Review article › peer-review

Abstract

The FOXO (Forkhead box O) transcription factors are implicated in several signaling pathways and play a vital role in various cellular and physiological processes include for instance, ROS (reactive oxygen spe-cies) response, cell proliferation, regulation of programmed cell death, longevity, metabolism and cancer and regulation of cell cycle. In humans, the four FOXO family members are responsible for resemblance in their structure, regulation and functions. FOXO1 gene is highly expressed in adipose tissues and it affects the regulation of glycogenolysis and gluconeogenesis through insulin signaling. The gene of FOXO3 is highly expressed in the kidney, heart, spleen and brain and is characterized as diverse forkhead DNA-binding domain of transcription factors. The FOXO3 is a tumor suppressor gene and found to interact with p53, the trigger for apoptosis through BCl2 family genes and a regulator of Notch signaling pathway for the self-renewal of stem cells. Therefore, FOXOs remains to be a fascinating and potential target to acquire novel therapeutic approaches to cure cancer. This review will provide a comprehensive overview about the biology of FOXO proteins, which can be utilized for developing current therapeutic approaches to treat cancer.

Original languageEnglish (US)
Pages (from-to)2839-2848
Number of pages10
JournalCurrent Pharmaceutical Design
Volume24
Issue number24
DOIs
StatePublished - 2018
Externally publishedYes

Keywords

  • Cancer
  • Cell proliferation
  • Forkhead box O
  • Polymorphism
  • Therapeutic
  • Transcription factors

ASJC Scopus subject areas

  • Pharmacology
  • Drug Discovery

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