ENhancing Cisd2 Expression to Retard Liver Aging

Yi Long Huang, Zhao Qing Shen, Ting Fen Tsai*

*Corresponding author for this work

Research output: Contribution to journalEditorial

1 Scopus citations


Liver is a pivotal metabolic organ that is responsible for xenobiotic detoxification, protein synthesis, bile production and energetic balance. Aging of the liver manifests as multiple functional and structural alterations [1]. Cisd2, the second member of the CDGSH iron-sulfur domain-containing protein family in mammals, has been shown to serve as an anti-aging protein that can modulate longevity and maintain cellular homeostasis [2]. Here our laboratory highlights a key factor underlying liver dysfunction during aging, which is a reduction in Cisd2 expression [3]. In a series of mouse studies, the robust protective effects of Cisd2 on age-associated or diet-induced liver damage were demonstrated. In agreement with the above, a persistently high level of Cisd2 appears to slow down the aging rate of liver in mice and the results are likely to be similar in humans (summarized in Figure 1A).

Original languageEnglish
Pages (from-to)1594-1596
Number of pages3
Issue number4
StatePublished - 2022


  • Cisd2
  • Liver aging
  • Non-alcoholic fatty liver disease
  • Oxidative stress
  • Proteomics
  • Transcriptomics


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