Regulators of Iron Homeostasis: New Players in Metabolism, Cell Death, and Disease

被引:1080
作者
Bogdan, Alexander R. [1 ]
Miyazawa, Masaki [1 ]
Hashimoto, Kazunori [1 ]
Tsuji, Yoshiaki [1 ]
机构
[1] N Carolina State Univ, Dept Biol Sci, Campus Box 7633, Raleigh, NC 27695 USA
基金
美国国家卫生研究院;
关键词
MOLECULAR-MECHANISMS; FERRITIN DEGRADATION; TRANSFERRIN RECEPTOR; CHAPERONES PCBP1; CANCER; ZIP14; DEFERASIROX; TRANSPORT; PROMOTES; FORM;
D O I
10.1016/j.tibs.2015.11.012
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Iron is necessary for life, but can also cause cell death. Accordingly, cells evolved a robust, tightly regulated suite of genes for maintaining iron homeostasis. Previous mechanistic studies on iron homeostasis have granted insight into the role of iron in human health and disease. We highlight new regulators of iron metabolism, including iron-trafficking proteins [solute carrier family 39, SLC39, also known as ZRT/IRT-like protein, ZIP; and poly-(rC)-binding protein, PCBP]:] and a cargo receptor (NCOA4) that is crucial for release of ferritin-bound iron. We also discuss emerging roles of iron in apoptosis and a novel iron dependent cell death pathway termed 'ferroptosis', the dysregulation of iron metabolism in human pathologies, and the use of iron chelators in cancer therapy.
引用
收藏
页码:274 / 286
页数:13
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