Research progress on the regulatory role of different cell death pathways in metabolic-dysfunction-associated

Congyue Zhang1, Mengjiao Sun1, Yuanjian Ding2

  • 1Department of Integrated Traditional Chinese and Western Medicine Hepatology, Hebei Medical University Third Hospital, Shijiazhuang, Hebei, China.

Insights

Metabolic dysfunction associated steatotic liver disease (MASLD) involves programmed cell death pathways. Understanding these cell death mechanisms is crucial for MASLD pathogenesis and treatment.

Area of Science:

  • Hepatology
  • Cell Biology
  • Molecular Medicine

Background:

  • Metabolic dysfunction associated steatotic liver disease (MASLD) is a prevalent chronic liver condition with significant health implications.
  • Programmed cell death is a fundamental biological process implicated in the development of various diseases, including MASLD.
  • MASLD pathogenesis involves complex cellular mechanisms, with programmed cell death playing a critical role.

Purpose of the Study:

  • To systematically review various forms of programmed cell death in MASLD.
  • To elucidate the regulatory mechanisms of different cell death pathways in MASLD.
  • To explore the synergistic interactions between distinct cell death modalities during MASLD progression.

Main Methods:

  • Systematic literature review of programmed cell death in MASLD.
  • Analysis of regulatory mechanisms for apoptosis, pyroptosis, autophagy, ferroptosis, and cuproptosis.
  • Examination of the interplay between different cell death types in MASLD stages.

Main Results:

  • Multiple programmed cell death pathways, including apoptosis, pyroptosis, autophagy, ferroptosis, and cuproptosis, are involved in MASLD.
  • These cell death pathways are intricately regulated and interact with each other.
  • Synergistic effects of various cell death forms are observed as MASLD advances through inflammation, fibrosis, and cirrhosis.

Conclusions:

  • Programmed cell death is a key player in the pathogenesis of MASLD.
  • Understanding the diverse and interacting cell death mechanisms offers novel therapeutic targets.
  • Further research into these pathways will enhance our comprehension of MASLD progression and management.

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