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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

科研成果: 期刊稿件文献综述同行评审

77 引用 (Scopus)

摘要

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.

源语言英语
页(从-至)2034-2042
页数9
期刊FEBS Letters
589
16
DOI
出版状态已出版 - 20 7月 2015

联合国可持续发展目标

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  1. 可持续发展目标 3 - 良好健康与福祉
    可持续发展目标 3 良好健康与福祉

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