Iron, Oxidative Stress, and Metabolic Dysfunction-Associated Steatotic Liver Disease

被引:30
作者
Gensluckner, Sophie [1 ,2 ]
Wernly, Bernhard [3 ]
Datz, Christian [3 ]
Aigner, Elmar [1 ,2 ]
机构
[1] Paracelsus Med Univ, Dept Internal Med 1, Mullner Hauptstr 48, A-5020 Salzburg, Austria
[2] Paracelsus Med Univ, Obes Res Unit, A-5020 Salzburg, Austria
[3] Paracelsus Med Univ, Gen Hosp Oberndorf, Dept Med, Teaching Hosp, A-5110 Oberndorf, Austria
关键词
iron metabolism; oxidative stress; ferroptosis; MASLD; liver fibrosis; HEPATOCELLULAR-CARCINOMA; CELL-DEATH; FERROPTOSIS; OVERLOAD; ACTIVATION; FIBROSIS; DYSREGULATION; HOMEOSTASIS; INJURY;
D O I
10.3390/antiox13020208
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
Excess free iron is a substrate for the formation of reactive oxygen species (ROS), thereby augmenting oxidative stress. Oxidative stress is a well-established cause of organ damage in the liver, the main site of iron storage. Ferroptosis, an iron-dependent mechanism of regulated cell death, has recently been gaining attention in the development of organ damage and the progression of liver disease. We therefore summarize the main mechanisms of iron metabolism, its close connection to oxidative stress and ferroptosis, and its particular relevance to disease mechanisms in metabolic-dysfunction-associated fatty liver disease and potential targets for therapy from a clinical perspective.
引用
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页数:12
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共 100 条
[31]   SLC39A14 Is Required for the Development of Hepatocellular Iron Overload in Murine Models of Hereditary Hemochromatosis [J].
Jenkitkasemwong, Supak ;
Wang, Chia-Yu ;
Coffey, Richard ;
Zhang, Wei ;
Chan, Alan ;
Biel, Thomas ;
Kim, Jae-Sung ;
Hojyo, Shintaro ;
Fukada, Toshiyuki ;
Knutson, Mitchell D. .
CELL METABOLISM, 2015, 22 (01) :138-150
[32]   Ferroptosis: mechanisms, biology and role in disease [J].
Jiang, Xuejun ;
Stockwell, Brent R. ;
Conrad, Marcus .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2021, 22 (04) :266-282
[33]   Basics and principles of cellular and systemic iron homeostasis [J].
Katsarou, Angeliki ;
Pantopoulos, Kostas .
MOLECULAR ASPECTS OF MEDICINE, 2020, 75
[34]   Transferrin and transferrin receptors update [J].
Kawabata, Hiroshi .
FREE RADICAL BIOLOGY AND MEDICINE, 2019, 133 :46-54
[35]   NRF2 addiction in cancer cells [J].
Kitamura, Hiroshi ;
Motohashi, Hozumi .
CANCER SCIENCE, 2018, 109 (04) :900-911
[36]   Artesunate alleviates liver fibrosis by regulating ferroptosis signaling pathway [J].
Kong, Zhaoyan ;
Liu, Rong ;
Cheng, Yuanrong .
BIOMEDICINE & PHARMACOTHERAPY, 2019, 109 :2043-2053
[37]   Serum ferritin is an independent predictor of histologic severity and advanced fibrosis in patients with nonalcoholic fatty liver disease [J].
Kowdley, Kris V. ;
Belt, Patricia ;
Wilson, Laura A. ;
Yeh, Matthew M. ;
Neuschwander-Tetri, Brent A. ;
Chalasani, Naga ;
Sanyal, Arun J. ;
Nelson, James E. .
HEPATOLOGY, 2012, 55 (01) :77-85
[38]   Targeting ferroptosis as a vulnerability in cancer [J].
Lei, Guang ;
Zhuang, Li ;
Gan, Boyi .
NATURE REVIEWS CANCER, 2022, 22 (07) :381-396
[39]   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)
[40]   Understanding sorafenib-induced ferroptosis and resistance mechanisms: Implications for cancer therapy [J].
Li, Qiuhong ;
Chen, Kexin ;
Zhang, Tianyi ;
Jiang, Donghui ;
Chen, Ligang ;
Jiang, Jun ;
Zhang, Chunxiang ;
Li, Shengbiao .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2023, 955