4.7 Review

The epigenetic regulators and metabolic changes in ferroptosis-associated cancer progression

期刊

MOLECULAR CANCER
卷 19, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12943-020-01157-x

关键词

Ferroptosis; Epigenetics; Cancer; Organelles; Chromatin remodeling factor; lncRNA; Golgi; Lysosome; Endoplasmic reticulum; Mitochondria; Metabolism; Iron; Lipid peroxidation; Immunotherapy

资金

  1. National Natural Science Foundation of China [81672991, 81874139, 81672787, 81772927]
  2. National Basic Research Program of China [2015CB553903]
  3. Overseas Expertise Introduction Project for Discipline Innovation (111 Project) [111-2-12]
  4. Hunan Provincial Key Area RD Programmes [2019SK2253]

向作者/读者索取更多资源

Ferroptosis, a novel form of regulated cell death, is different from other types of cell death in morphology, genetics and biochemistry. Increasing evidence indicates that ferroptosis has significant implications on cell death linked to cardiomyopathy, tumorigenesis, and cerebral hemorrhage to name a few. Here we summarize current literature on ferroptosis, including organelle dysfunction, signaling transduction pathways, metabolic reprogramming and epigenetic regulators in cancer progression. With regard to organelles, mitochondria-induced cysteine starvation, endoplasmic reticulum-related oxidative stress, lysosome dysfunction and golgi stress-related lipid peroxidation all contribute to induction of ferroptosis. Understanding the underlying mechanism in ferroptosis could provide insight into the treatment of various intractable diseases including cancers.

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

4.7
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