Potential therapies for HCC involving targeting the ferroptosis pathway

被引:0
作者
Li, Denghui [1 ]
Zhang, Mengjie [1 ]
Liu, Ju [2 ]
Li, Zhifang [2 ]
Ni, Bing [1 ]
机构
[1] Third Mil Med Univ, Coll High Altitude Mil Med, Dept Pathophysiol, Chongqing 400038, Peoples R China
[2] Third Mil Med Univ, Coll Basic Med Sci, Dept Foreign Languages, Chongqing 400038, Peoples R China
基金
中国国家自然科学基金;
关键词
Hepatocellular carcinoma; ferroptosis; therapy; positive regulation; negative regulation; HEPATOCELLULAR-CARCINOMA CELLS; PROMOTES FERROPTOSIS; INHIBITS FERROPTOSIS; LIPID-PEROXIDATION; OXIDATIVE STRESS; CANCER; DEATH; IRON; GLUTATHIONE; ACTIVATION;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Liver cancer ranks as the third leading cause of cancer-related mortality worldwide, predominantly in the form of hepatocellular carcinoma (HCC). Conventional detection and treatment approaches have proven inadequate for addressing the elevated incidence and mortality rates associated with HCC. However, a significant body of research suggests that combating HCC through the induction of ferroptosis is possible. Ferroptosis is a regulated cell death process characterized by elevated levels of reactive oxygen species (ROS) and lipid peroxide accumulation, both of which are dependent on iron levels. In recent years, there has been an increasing focus on investigating ferroptosis, revealing its potential as an inhibitory mechanism against various diseases, including tumors. Therefore, ferroptosis induction holds great promise for treating multiple types of cancers, including HCC. This article provides a review of the key mechanisms involved in ferroptosis and explores the potential application of multiple targets and pathways associated with ferroptosis in HCC treatment to improve therapeutic outcomes.
引用
收藏
页码:1446 / 1465
页数:20
相关论文
共 162 条
[1]   Five-Membered Ring Peroxide Selectively Initiates Ferroptosis in Cancer Cells [J].
Abrams, Rachel P. ;
Carroll, William L. ;
Woerpel, K. A. .
ACS CHEMICAL BIOLOGY, 2016, 11 (05) :1305-1312
[2]   Heme oxygenase-1 mitigates ferroptosis in renal proximal tubule cells [J].
Adedoyin, Oreoluwa ;
Boddu, Ravindra ;
Traylor, Amie ;
Lever, Jeremie M. ;
Bolisetty, Subhashini ;
George, James F. ;
Agarwal, Anupam .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2018, 314 (05) :F702-F714
[3]   An Endoperoxide Reactivity-Based FRET Probe for Ratiometric Fluorescence Imaging of Labile Iron Pools in Living Cells [J].
Aron, Allegra T. ;
Loehr, Morten O. ;
Bogena, Jana ;
Chang, Christopher J. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2016, 138 (43) :14338-14346
[4]  
Averill-Bates DA, 2023, VITAM HORM, V121, P109, DOI 10.1016/bs.vh.2022.09.002
[5]   miR-148a regulates expression of the transferrin receptor 1 in hepatocellular carcinoma [J].
Babu, Kamesh R. ;
Muckenthaler, Martina U. .
SCIENTIFIC REPORTS, 2019, 9 (1)
[6]   MicroRNA-214-3p enhances erastin-induced ferroptosis by targeting ATF4 in hepatoma cells [J].
Bai, Tao ;
Liang, Ruopeng ;
Zhu, Rongtao ;
Wang, Weijie ;
Zhou, Lin ;
Sun, Yuling .
JOURNAL OF CELLULAR PHYSIOLOGY, 2020, 235 (7-8) :5637-5648
[7]   Sigma-1 receptor protects against ferroptosis in hepatocellular carcinoma cells [J].
Bai, Tao ;
Lei, Pengxu ;
Zhou, Hao ;
Liang, Ruopeng ;
Zhu, Rongtao ;
Wang, Weijie ;
Zhou, Lin ;
Sun, Yuling .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2019, 23 (11) :7349-7359
[8]   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
[9]   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-+
[10]   Unravelling mechanisms of p53-mediated tumour suppression [J].
Bieging, Kathryn T. ;
Mello, Stephano Spano ;
Attardi, Laura D. .
NATURE REVIEWS CANCER, 2014, 14 (05) :359-370