Inducing ferroptosis has the potential to overcome therapy resistance in breast cancer

被引:25
作者
Qi, Xiaowen [1 ]
Wan, Zhixing [1 ]
Jiang, Baohong [2 ]
Ouyang, Yuhan [1 ]
Feng, Wenjie [1 ]
Zhu, Hongbo [1 ]
Tan, Yeru [1 ]
He, Rongfang [3 ]
Xie, Liming [1 ]
Li, Yuehua [1 ,4 ]
机构
[1] Univ South China, Affiliated Hosp 1, Hengyang Med Sch, Dept Med Oncol, Hengyang, Hunan, Peoples R China
[2] Univ South China, Affiliated Hosp 1, Hengyang Med Sch, Dept Pharm, Hengyang, Hunan, Peoples R China
[3] Univ South China, Affiliated Hosp 1, Hengyang Med Sch, Dept Pathol, Hengyang, Hunan, Peoples R China
[4] Univ South China, Inst Pathogen Biol, Hengyang Med Coll, Hengyang, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
ferroptosis; breast cancer; therapy resistance; autophagy; chemotherapy; radiotherapy; nanoparticles; STRESS-INDUCED FERROPTOSIS; PHASE-II TRIAL; TUMOR MICROENVIRONMENT; GTP CYCLOHYDROLASE; ANTIOXIDANT ROLE; IRON-METABOLISM; OPEN-LABEL; GLUTATHIONE; P53; OXYGENASE-1;
D O I
10.3389/fimmu.2022.1038225
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Breast cancer is the most common type of malignancy among women. Due to the iron-dependent character of breast cancer cells, they are more sensitive to ferroptosis compared to normal cells. It is possible to reverse tumor resistance by inducing ferroptosis in breast cancer cells, thereby improving tumor treatment outcomes. Ferroptosis is highly dependent on the balance of oxidative and antioxidant status. When ferroptosis occurs, intracellular iron levels are significantly increased, leading to increased membrane lipid peroxidation and ultimately triggering ferroptosis. Ferroptotic death is a form of autophagy-associated cell death. Synergistic use of nanoparticle-loaded ferroptosis-inducer with radiotherapy and chemotherapy achieves more significant tumor suppression and inhibits the growth of breast cancer by targeting cancer tissues, enhancing the sensitivity of cells to drugs, reducing the drug resistance of cancer cells and the toxicity of drugs. In this review, we present the current status of breast cancer and the mechanisms of ferroptosis. It is hopeful for us to realize effective treatment of breast cancer through targeted ferroptosis.
引用
收藏
页数:16
相关论文
共 171 条
[31]   Autophagy-dependent ferroptosis drives tumor-associated macrophage polarization via release and uptake of oncogenic KRAS protein [J].
Dai, Enyong ;
Han, Leng ;
Liu, Jiao ;
Xie, Yangchun ;
Kroemer, Guido ;
Klionsky, Daniel J. ;
Zeh, Herbert J. ;
Kang, Rui ;
Wang, Jing ;
Tang, Daolin .
AUTOPHAGY, 2020, 16 (11) :2069-2083
[32]   The pharmacological point of view of resistance to therapy in tumors [J].
Damia, Giovanna ;
Garattini, Silvio .
CANCER TREATMENT REVIEWS, 2014, 40 (08) :909-916
[33]   Zim17/Tim15 links mitochondrial iron-sulfur cluster biosynthesis to nuclear genome stability [J].
del Carmen Diaz de la Loza, Maria ;
Gallardo, Mercedes ;
Luisa Garcia-Rubio, Maria ;
Izquierdo, Alicia ;
Herrero, Enrique ;
Aguilera, Andres ;
Erik Wellinger, Ralf .
NUCLEIC ACIDS RESEARCH, 2011, 39 (14) :6002-6015
[34]   Autophagy-dependent cell death [J].
Denton, Donna ;
Kumar, Sharad .
CELL DEATH AND DIFFERENTIATION, 2019, 26 (04) :605-616
[35]   Mechanism and medical implications of mammalian autophagy [J].
Dikic, Ivan ;
Elazar, Zvulun .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2018, 19 (06) :349-364
[36]   Human Haploid Cell Genetics Reveals Roles for Lipid Metabolism Genes in Nonapoptotic Cell Death [J].
Dixon, Scott J. ;
Winter, Georg E. ;
Musavi, Leila S. ;
Lee, Eric D. ;
Snijder, Berend ;
Rebsamen, Manuele ;
Superti-Furga, Giulio ;
Stockwell, Brent R. .
ACS CHEMICAL BIOLOGY, 2015, 10 (07) :1604-1609
[37]   The role of iron and reactive oxygen species in cell death [J].
Dixon, Scott J. ;
Stockwell, Brent R. .
NATURE CHEMICAL BIOLOGY, 2014, 10 (01) :9-17
[38]   Ferroptosis: An Iron-Dependent Form of Nonapoptotic Cell Death [J].
Dixon, Scott J. ;
Lemberg, Kathryn M. ;
Lamprecht, Michael R. ;
Skouta, Rachid ;
Zaitsev, Eleina M. ;
Gleason, Caroline E. ;
Patel, Darpan N. ;
Bauer, Andras J. ;
Cantley, Alexandra M. ;
Yang, Wan Seok ;
Morrison, Barclay, III ;
Stockwell, Brent R. .
CELL, 2012, 149 (05) :1060-1072
[39]   NRF2 plays a critical role in mitigating lipid peroxidation and ferroptosis [J].
Dodson, Matthew ;
Castro-Portuguez, Raul ;
Zhang, Donna D. .
REDOX BIOLOGY, 2019, 23
[40]   FSP1 is a glutathione-independent ferroptosis suppressor [J].
Doll, Sebastian ;
Freitas, Florencio Porto ;
Shah, Ron ;
Aldrovandi, Maceler ;
da Silva, Milene Costa ;
Ingold, Irina ;
Grocin, Andrea Goya ;
da Silva, Thamara Nishida Xavier ;
Panzilius, Elena ;
Scheel, Christina H. ;
Mourao, Andre ;
Buday, Katalin ;
Sato, Mami ;
Wanninger, Jonas ;
Vignane, Thibaut ;
Mohana, Vaishnavi ;
Rehberg, Markus ;
Flatley, Andrew ;
Schepers, Aloys ;
Kurz, Andreas ;
White, Daniel ;
Sauer, Markus ;
Sattler, Michael ;
Tate, Edward William ;
Schmitz, Werner ;
Schulze, Almut ;
O'Donnell, Valerie ;
Proneth, Bettina ;
Popowicz, Grzegorz M. ;
Pratt, Derek A. ;
Angeli, Jose Pedro Friedmann ;
Conrad, Marcus .
NATURE, 2019, 575 (7784) :693-+