Crosstalk between ferroptosis and steroid hormone signaling in gynecologic cancers

被引:1
|
作者
Lai, Wen [1 ]
Chen, Jianquan [2 ]
Wang, Tianming [2 ]
Liu, Qiaoling [1 ]
机构
[1] Nanjing Med Univ, Affiliated Jiangning Hosp, Dept Obstet & Gynecol, Nanjing, Peoples R China
[2] Nanjing Med Univ, Affiliated Jiangning Hosp, Translat Med Res Ctr, Cent Lab, Nanjing, Peoples R China
关键词
ferroptosis; lipid peroxidation; gynecologic cancers; estrogen; progesterone; ESTROGEN-RECEPTOR-BETA; SEROUS OVARIAN-CANCER; CELL-DEATH; ENDOMETRIAL CANCER; MOLECULAR-MECHANISMS; IRON OVERLOAD; CYSTINE/GLUTAMATE ANTIPORTER; CYTOCHROME-P450; 17A1; IMMUNE INFILTRATION; MEVALONATE PATHWAY;
D O I
10.3389/fmolb.2023.1223493
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ferroptosis is a novel types of regulated cell death and is widely studied in cancers and many other diseases in recent years. It is characterized by iron accumulation and intense lipid peroxidation that ultimately inducing oxidative damage. So far, signaling pathways related to ferroptosis are involved in all aspects of determining cell fate, including oxidative phosphorylation, metal-ion transport, energy metabolism and cholesterol synthesis progress, et al. Recently, accumulated studies have demonstrated that ferroptosis is associated with gynecological oncology related to steroid hormone signaling. This review trends to summarize the mechanisms and applications of ferroptosis in cancers related to estrogen and progesterone, which is expected to provide a theoretical basis for the prevention and treatment of gynecologic cancers.
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收藏
页数:15
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