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SIRT1 is a regulator of autophagy: Implications in gastric cancer progression and treatment

  • Guanglin Qiu
  • , Xuqi Li
  • , Xiangming Che
  • , Chao Wei
  • , Shicai He
  • , Jing Lu
  • , Zongliang Jia
  • , Ke Pang
  • , Lin Fan
  • Xi'an Jiaotong University
  • Xi'an Health School
  • Shaanxi Friendship Hospital

Research output: Contribution to journalReview articlepeer-review

77 Scopus citations

Abstract

Silent mating type information regulation 1 (SIRT1) is implicated in tumorigenesis through its effect on autophagy. In gastric cancer (GC), SIRT1 is a marker for prognosis and is involved in cell invasion, proliferation, epithelial-mesenchymal transition (EMT) and drug resistance. Autophagy can function as a cell-survival mechanism or lead to cell death during the genesis and treatment of GC. This functionality is determined by factors including the stage of the tumor, cellular context and stress levels. Interestingly, SIRT1 can regulate autophagy through the deacetylation of autophagy-related genes (ATGs) and mediators of autophagy. Taken together, these findings support the need for continued research efforts to understand the mechanisms mediating the development of gastric cancer and unveil new strategies to eradicate this disease.

Original languageEnglish
Pages (from-to)2034-2042
Number of pages9
JournalFEBS Letters
Volume589
Issue number16
DOIs
StatePublished - 20 Jul 2015

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Autophagy
  • Gastric cancer
  • Silent mating type information regulation 1
  • Tumor promoter
  • Tumor suppressor

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