Ferroptosis in Cancer: Mechanism and Therapeutic Potential

被引:0
作者
Singh, Mansaa [1 ]
Arora, Hasmiq L. [1 ]
Naik, Rutuja [1 ]
Joshi, Shravani [1 ]
Sonawane, Kaveri [1 ]
Sharma, Nilesh Kumar [1 ]
Sinha, Birandra K. [2 ]
机构
[1] Dr DY Patil Vidyapeeth, Dr DY Patil Biotechnol & Bioinformat Inst, Canc & Translat Res Lab, Pune 411033, India
[2] Natl Inst Environm Hlth Sci, Div Translat Toxicol, Mechanist Toxicol Branch, Durham, NC 27709 USA
关键词
ferroptosis; cell death; signaling; oxidative stress; iron; lipid peroxidation; PROGRAMMED CELL-DEATH; LIPID-PEROXIDATION; IRON-METABOLISM; OXIDATIVE STRESS; REDOX BIOLOGY; APOPTOSIS; AUTOPHAGY; RESISTANCE; HALLMARKS; PATHWAYS;
D O I
10.3390/ijms26083852
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
Cancer drug resistance occurs when cancer cells evade cell death following treatment with chemotherapy, radiation therapy, and targeted therapies. This resistance is often linked to the reprogramming of programmed cell death (PCD) pathways, allowing cancer cells to survive drug-induced stress. However, certain anticancer therapies, when combined with specific agents or inhibitors, can induce ferroptosis-a form of cell death driven by iron-dependent lipid peroxidation. Currently, extensive preclinical and clinical research is underway to investigate the molecular, cellular, and tissue-specific mechanisms underlying ferroptosis, with the goal of identifying strategies to overcome drug resistance in cancers unresponsive to conventional PCD pathways. By harnessing ferroptosis, cancer cells can be compelled to undergo lipid peroxidation-induced death, potentially improving therapeutic outcomes in patients with cancer. This short review aims to enhance the understanding of ferroptosis inducers in cancer therapy and stimulate further research into ferroptosis-based approaches for more effective clinical cancer treatment.
引用
收藏
页数:18
相关论文
共 179 条
[81]   Targeting ferroptosis as a vulnerability in cancer [J].
Lei, Guang ;
Zhuang, Li ;
Gan, Boyi .
NATURE REVIEWS CANCER, 2022, 22 (07) :381-396
[82]   The role of ferroptosis in ionizing radiation-induced cell death and tumor suppression [J].
Lei, Guang ;
Zhang, Yilei ;
Koppula, Pranavi ;
Liu, Xiaoguang ;
Zhang, Jie ;
Lin, Steven H. ;
Ajani, Jaffer A. ;
Xiao, Qin ;
Liao, Zhongxing ;
Wang, Hui ;
Gan, Boyi .
CELL RESEARCH, 2020, 30 (02) :146-162
[83]   The first 30 years of p53: growing ever more complex [J].
Levine, Arnold J. ;
Oren, Moshe .
NATURE REVIEWS CANCER, 2009, 9 (10) :749-758
[84]   The interaction between ferroptosis and lipid metabolism in cancer [J].
Li, Dingshan ;
Li, Yongsheng .
SIGNAL TRANSDUCTION AND TARGETED THERAPY, 2020, 5 (01)
[85]   System Xc-/GSH/GPX4 axis: An important antioxidant system for the ferroptosis in drug-resistant solid tumor therapy [J].
Li, Feng-Jiao ;
Long, Hui-Zhi ;
Zhou, Zi-Wei ;
Luo, Hong-Yu ;
Xu, Shuo-Guo ;
Gao, Li-Chen .
FRONTIERS IN PHARMACOLOGY, 2022, 13
[86]   Ferroptosis: past, present and future [J].
Li, Jie ;
Cao, Feng ;
Yin, He-liang ;
Huang, Zi-jian ;
Lin, Zhi-tao ;
Mao, Ning ;
Sun, Bei ;
Wang, Gang .
CELL DEATH & DISEASE, 2020, 11 (02)
[87]   Dual Ratio and Ultraprecision Quantification of Mitochondrial Viscosity in Ferroptosis Enabled by a Vibration-Based Triple-Emission Fluorescent Probe [J].
Li, Lu ;
Huang, Yidan ;
Jin, Xin ;
Wang, Qiaochun ;
Su, Jianhua ;
Guo, Lifang .
ANALYTICAL CHEMISTRY, 2023, 95 (46) :17003-17010
[88]   Synergistic suppression of ovarian cancer by combining NRF2 and GPX4 inhibitors: in vitro and in vivo evidence [J].
Li, Ning ;
Jiang, Xingmei ;
Zhang, Qingyu ;
Huang, Yongmei ;
Wei, Jinbin ;
Zhang, Haitao ;
Luo, Hui .
JOURNAL OF OVARIAN RESEARCH, 2024, 17 (01)
[89]   FSP1: a key regulator of ferroptosis [J].
Li, Wentao ;
Liang, Lin ;
Liu, Siyi ;
Yi, Hong ;
Zhou, Yanhong .
TRENDS IN MOLECULAR MEDICINE, 2023, 29 (09) :753-764
[90]   Cisplatin synergizes with PRLX93936 to induce ferroptosis in non-small cell lung cancer cells [J].
Liang, Zhigang ;
Zhao, Weijun ;
Li, Xinjian ;
Wang, Longfei ;
Meng, Lifei ;
Yu, Rui .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2021, 569 :79-85