3.8 Article

Autophagy and Ferroptosis-What Is the Connection?

期刊

CURRENT PATHOBIOLOGY REPORTS
卷 5, 期 2, 页码 153-159

出版社

SPRINGER
DOI: 10.1007/s40139-017-0139-5

关键词

Ferroptosis; Autophagy; Signal transduction; Molecular interaction; Lipid peroxidation; Iron metabolism

资金

  1. National Institutes of Health of the USA [R01GM115366, R01CA160417]
  2. National Natural Science Foundation of China [31671435]
  3. National Natural Science Foundation of Guangdong [2016A030308]
  4. American Cancer Society [RSG-16-014-01-CDD]

向作者/读者索取更多资源

Purpose of Review Autophagy is a conserved intracellular degradation system and plays a dual role in cell death, depending on context and phase. Ferroptosis is a new form of regulated cell death that mainly depends on iron accumulation and lipid peroxidation. In this review, we summarize the processes of autophagy and ferroptosis and discuss their crosstalk mechanisms at the molecular level. Recent Findings The original study shows that ferroptosis is morphologically, biochemically, and genetically distinct from autophagy and other types of cell death. However, recent studies demonstrate that activation of ferroptosis is indeed dependent on the induction of autophagy. Additionally, many ferroptosis regulators such as SLC7A11, GPX4, NRF2, p53, HSPB1, CISD1, FANCD2, and ACSL4 have been identified as potential regulators of autophagy. Summary This review not only highlights the importance of autophagy as an emerging mechanism of ferroptosis but also raises new insights regarding regulated cell death.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

3.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据