Ferroptosis: A New Strategy for Cancer Therapy

被引:20
作者
Chen, Yu [1 ]
Fan, Zhihua [2 ]
Hu, Shen [3 ]
Lu, Chengchao [1 ]
Xiang, Yi [1 ]
Liao, Shuzhi [1 ]
机构
[1] Guangdong Women & Children Hosp, Dept Pediat Surg, Guangzhou, Peoples R China
[2] Cent South Univ, Xiangya Hosp, Dept Dermatol, Changsha, Peoples R China
[3] Zhejiang Univ, Affiliated Hosp 2, Dept Obstet, Sch Med, Hangzhou, Peoples R China
关键词
ferroptosis; cancer; iron; programmed cell death; clinical application; ERASTIN-INDUCED FERROPTOSIS; CELL-DEATH; TRANSSULFURATION PATHWAY; LIPID-PEROXIDATION; IRON; TEMOZOLOMIDE; INHIBITION; METABOLISM; ACTIVATION; FORM;
D O I
10.3389/fonc.2022.830561
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Ferroptosis is a newly discovered form of iron-dependent cell death, which is different from other death forms. The main characteristics of ferroptosis are: (1) Amino acid metabolism. (2) Iron metabolism; (3) Lipid metabolism and Reactive oxygen species (ROS). Ferroptosis is related to the occurrence and development of a variety of cancers, especially in the drug resistance. This article reviews the research progress of iron death in tumors, and provides a theoretical reference for its further research and clinical application.
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页数:8
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共 75 条
[1]  
Akatsuka Shinya, 2016, Nihon Rinsho, V74, P1168
[2]   Iron homeostasis [J].
Andrews, Nancy C. ;
Schmidt, Paul J. .
ANNUAL REVIEW OF PHYSIOLOGY, 2007, 69 :69-85
[3]   Ferroptosis Inhibition: Mechanisms and Opportunities [J].
Angeli, Jose Pedro Friedmann ;
Shah, Ron ;
Pratt, Derek A. ;
Conrad, Marcus .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2017, 38 (05) :489-498
[4]   Reactive oxygen species: Metabolism, oxidative stress, and signal transduction [J].
Apel, K ;
Hirt, H .
ANNUAL REVIEW OF PLANT BIOLOGY, 2004, 55 :373-399
[5]   Haloperidol, a sigma receptor 1 antagonist, promotes ferroptosis in hepatocellular carcinoma cells [J].
Bai, Tao ;
Wang, Shuai ;
Zhao, Yipu ;
Zhu, Rongtao ;
Wang, Weijie ;
Sun, Yuling .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2017, 491 (04) :919-925
[6]   Iron addiction: a novel therapeutic target in ovarian cancer [J].
Basuli, D. ;
Tesfay, L. ;
Deng, Z. ;
Paul, B. ;
Yamamoto, Y. ;
Ning, G. ;
Xian, W. ;
McKeon, F. ;
Lynch, M. ;
Crum, C. P. ;
Hegde, P. ;
Brewer, M. ;
Wang, X. ;
Miller, L. D. ;
Dyment, N. ;
Torti, F. M. ;
Torti, S. V. .
ONCOGENE, 2017, 36 (29) :4089-4099
[7]   The CoQ oxidoreductase FSP1 acts parallel to GPX4 to inhibit ferroptosis [J].
Bersuker, Kirill ;
Hendricks, Joseph M. ;
Li, Zhipeng ;
Magtanong, Leslie ;
Ford, Breanna ;
Tang, Peter H. ;
Roberts, Melissa A. ;
Tong, Bingqi ;
Maimone, Thomas J. ;
Zoncu, Roberto ;
Bassik, Michael C. ;
Nomura, Daniel K. ;
Dixon, Scott J. ;
Olzmann, James A. .
NATURE, 2019, 575 (7784) :688-+
[8]   Current and future strategies for treatment of glioma [J].
Bush, Nancy Ann Oberheim ;
Chang, Susan M. ;
Berger, Mitchel S. .
NEUROSURGICAL REVIEW, 2017, 40 (01) :1-14
[9]   Stearoyl CoA Desaturase Regulates Ferroptosis in Ovarian Cancer Offering New Therapeutic Perspectives [J].
Carbone, Michele ;
Melino, Gerry .
CANCER RESEARCH, 2019, 79 (20) :5149-5150
[10]   Role of cystathionine beta synthase in lipid metabolism in ovarian cancer [J].
Chakraborty, Prabir K. ;
Xiong, Xunhao ;
Mustafi, Soumyajit Banerjee ;
Saha, Sounik ;
Dhanasekaran, Danny ;
Mandal, Nawajes A. ;
McMeekin, Scott ;
Bhattacharya, Resham ;
Mukherjee, Priyabrata .
ONCOTARGET, 2015, 6 (35) :37367-37384