Copper in hepatocellular carcinoma: A double-edged sword with therapeutic potentials

被引:31
作者
Wu, Zixin [1 ,2 ,3 ]
Lv, Guishuai [2 ,3 ]
Xing, Fuxue [1 ,2 ,3 ]
Xiang, Wei [1 ,2 ,3 ]
Ma, Yue [1 ,2 ,3 ]
Feng, Qiyu [1 ,2 ,3 ]
Yang, Wen [1 ,2 ,3 ]
Wang, Hongyang [1 ,2 ,3 ]
机构
[1] Univ Sci & Technol China, USTC, Affiliated Hosp 1, Div Life Sci & Med,Canc Res Ctr, Hefei 230001, Anhui, Peoples R China
[2] Second Mil Med Univ, Eastern Hepatobiliary Surg Inst Hosp, Int Cooperat Lab Signal Transduct, Shanghai 200438, Peoples R China
[3] Second Mil Med Univ, Natl Ctr Liver Canc, Shanghai 201805, Peoples R China
基金
中国国家自然科学基金;
关键词
Copper; Copper homeostasis; Hepatocellular carcinoma; Cuproptosis; Cancer therapy; ANTICANCER DRUG CISPLATIN; CHELATING AGENT; CELLULAR PHARMACOLOGY; BREAST-CANCER; SACCHAROMYCES-CEREVISIAE; TRANSPORTER CTR1; TARGETING COPPER; TUMOR-GROWTH; ANGIOGENESIS; TRIENTINE;
D O I
10.1016/j.canlet.2023.216348
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Copper is a necessary cofactor vital for maintaining biological functions, as well as participating in the development of cancer. A plethora of studies have demonstrated that copper is a double-edged sword, presenting both benefits and detriments to tumors. The liver is a metabolically active organ, and an imbalance of copper homeostasis can result in deleterious consequences to the liver. Hepatocellular carcinoma (HCC), the most common primary liver cancer, is a highly aggressive malignancy with limited viable therapeutic options. As research advances, the focus has shifted towards the relationships between copper and HCC. Innovatively, cuproplasia and cuproptosis have been proposed to depict copper-related cellular growth and death, providing new insights for HCC treatment. By summarizing the constantly elucidated molecular connections, this review discusses the mechanisms of copper in the pathogenesis, progression, and potential therapeutics of HCC. Additionally, we aim to tentatively provide a theoretical foundation and gospel for HCC patients.
引用
收藏
页数:12
相关论文
共 164 条
[1]   Wilson disease [J].
Aggarwal, Annu ;
Bhatt, Mohit .
CURRENT OPINION IN NEUROLOGY, 2020, 33 (04) :534-542
[2]  
Aggett P J, 1999, Eur J Med Res, V4, P214
[3]   The Burden of Primary Liver Cancer and Underlying Etiologies From 1990 to 2015 at the Global, Regional, and National Level Results From the Global Burden of Disease Study 2015 [J].
Akinyemiju, Tomi ;
Abera, Semaw ;
Ahmed, Muktar ;
Alam, Noore ;
Alemayohu, Mulubirhan Assefa ;
Allen, Christine ;
Al-Raddadi, Rajaa ;
Alvis-Guzman, Nelson ;
Amoako, Yaw ;
Artaman, Al ;
Ayele, Tadesse Awoke ;
Barac, Aleksandra ;
Bensenor, Isabela ;
Berhane, Adugnaw ;
Bhutta, Zulfiqar ;
Castillo-Rivas, Jacqueline ;
Chitheer, Abdulaal ;
Choi, Jee-Young ;
Cowie, Benjamin ;
Dandona, Lalit ;
Dandona, Rakhi ;
Dey, Subhojit ;
Dicker, Daniel ;
Phuc, Huyen ;
Ekwueme, Donatus U. ;
Zaki, Maysaa El Sayed ;
Fischer, Florian ;
Furst, Thomas ;
Hancock, Jamie ;
Hay, Simon I. ;
Hotez, Peter ;
Jee, Sun Ha ;
Kasaeian, Amir ;
Khader, Yousef ;
Khang, Young-Ho ;
Kumar, G. Anil ;
Kutz, Michael ;
Larson, Heidi ;
Lopez, Alan ;
Lunevicius, Raimundas ;
Malekzadeh, Reza ;
McAlinden, Colm ;
Meier, Toni ;
Mendoza, Walter ;
Mokdad, Ali ;
Moradi-Lakeh, Maziar ;
Nagel, Gabriele ;
Nguyen, Quyen ;
Nguyen, Grant ;
Ogbo, Felix .
JAMA ONCOLOGY, 2017, 3 (12) :1683-1691
[4]   Targeting Lipid Metabolism in Liver Cancer [J].
Alannan, Malak ;
Fayyad-Kazan, Hussein ;
Trezeguet, Veronique ;
Merched, Aksam .
BIOCHEMISTRY, 2020, 59 (41) :3951-3964
[5]   The P-type ATPase transporter ATP7A promotes angiogenesis by limiting autophagic degradation of VEGFR2 [J].
Ash, Dipankar ;
Sudhahar, Varadarajan ;
Youn, Seock-Won ;
Okur, Mustafa Nazir ;
Das, Archita ;
O'Bryan, John P. ;
McMenamin, Maggie ;
Hou, Yali ;
Kaplan, Jack H. ;
Fukai, Tohru ;
Ushio-Fukai, Masuko .
NATURE COMMUNICATIONS, 2021, 12 (01)
[6]   What is your diagnosis? Photoclinic Diagnosis Menkes Disease [J].
Ashrafi, Mahmoud Reza ;
Ghasemi, Dorsa ;
Safavi, Moeinadin .
ARCHIVES OF IRANIAN MEDICINE, 2021, 24 (12) :919-920
[7]   Mitochondrial copper(I) transfer from Cox17 to Sco1 is coupled to electron transfer [J].
Banci, Lucia ;
Bertini, Ivano ;
Ciofi-Baffoni, Simone ;
Hadjiloi, Theodoros ;
Martinelli, Manuele ;
Palumaa, Peep .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (19) :6803-6808
[8]   A hydrogen peroxide -activated Cu(II) pro-ionophore strategy for modifying naphthazarin as a promising anticancer agent with high selectivity for generating ROS in HepG2 cells over in L02 cells [J].
Bao, Xia-Zhen ;
Wang, Qi ;
Ren, Xiao-Rong ;
Dai, Fang ;
Zhou, Bo .
FREE RADICAL BIOLOGY AND MEDICINE, 2020, 152 :597-608
[9]   Mitochondrial Electron Transport Chain in Heavy Metal-Induced Neurotoxicity: Effects of Cadmium, Mercury, and Copper [J].
Belyaeva, Elena A. ;
Sokolova, Tatyana V. ;
Emelyanova, Larisa V. ;
Zakharova, Irina O. .
SCIENTIFIC WORLD JOURNAL, 2012,
[10]   Activating Platinum Anticancer Complexes with Visible Light [J].
Berners-Price, Susan J. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2011, 50 (04) :804-805