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铁在肝细胞癌中的作用。

Iron at the Interface of Hepatocellular Carcinoma.

机构信息

Institute of Comparative Molecular Endocrinology, Ulm University, 89081 Ulm, Germany.

Department of Internal Medicine I, University Hospital Ulm, 89081 Ulm, Germany.

出版信息

Int J Mol Sci. 2021 Apr 15;22(8):4097. doi: 10.3390/ijms22084097.

DOI:10.3390/ijms22084097
PMID:33921027
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8071427/
Abstract

Cancer incidence and mortality are rapidly growing, with liver cancer being the sixth most diagnosed cancer worldwide and the third leading cause of cancer death in 2020. A number of risk factors have been identified that trigger the progression to hepatocellular carcinoma. In this review, we focus on iron as a potential risk factor for liver carcinogenesis. Molecules involved in the regulation of iron metabolism are often upregulated in cancer cells, in order to provide a supply of this essential trace element for all stages of tumor development, survival, proliferation, and metastasis. Thus, cellular and systemic iron levels must be tightly regulated to prevent or delay liver cancer progression. Disorders associated with dysregulated iron metabolism are characterized with increased susceptibility to hepatocellular carcinoma. This review discusses the association of iron with metabolic disorders such as hereditary hemochromatosis, non-alcoholic fatty liver disease, obesity, and type 2 diabetes, in the background of hepatocellular carcinoma.

摘要

癌症的发病率和死亡率正在迅速上升,肝癌是全球第六大常见癌症,也是 2020 年癌症死亡的第三大主要原因。已经确定了许多引发肝细胞癌进展的危险因素。在这篇综述中,我们重点关注铁作为肝癌发生的潜在危险因素。参与铁代谢调节的分子在癌细胞中经常上调,以便为肿瘤发展的所有阶段、生存、增殖和转移提供这种必需的微量元素供应。因此,必须严格调节细胞内和系统内的铁水平,以防止或延缓肝癌的进展。与铁代谢失调相关的疾病的特点是更容易发生肝细胞癌。本综述讨论了铁与遗传性血色素沉着症、非酒精性脂肪性肝病、肥胖症和 2 型糖尿病等代谢紊乱之间的关联,这些疾病都是在肝细胞癌的背景下发生的。

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本文引用的文献

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Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries.《全球癌症统计数据 2020:全球 185 个国家和地区 36 种癌症的发病率和死亡率估计》。
CA Cancer J Clin. 2021 May;71(3):209-249. doi: 10.3322/caac.21660. Epub 2021 Feb 4.
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Iron: An Essential Element of Cancer Metabolism.铁:癌症代谢的必需元素。
Cells. 2020 Dec 3;9(12):2591. doi: 10.3390/cells9122591.
3
Viral Hepatitis and Iron Dysregulation: Molecular Pathways and the Role of Lactoferrin.病毒性肝炎与铁代谢失调:分子途径及乳铁蛋白的作用
Molecules. 2020 Apr 24;25(8):1997. doi: 10.3390/molecules25081997.
4
Altered Iron Metabolism and Impact in Cancer Biology, Metastasis, and Immunology.铁代谢改变及其在癌症生物学、转移和免疫学中的影响。
Front Oncol. 2020 Apr 9;10:476. doi: 10.3389/fonc.2020.00476. eCollection 2020.
5
Iron Metabolism in Cancer Progression.癌症进展中的铁代谢。
Int J Mol Sci. 2020 Mar 24;21(6):2257. doi: 10.3390/ijms21062257.
6
Reclassifying Hepatic Cell Death during Liver Damage: Ferroptosis-A Novel Form of Non-Apoptotic Cell Death?在肝损伤过程中重新分类肝细胞死亡:铁死亡——一种新的非细胞凋亡性细胞死亡形式?
Int J Mol Sci. 2020 Feb 28;21(5):1651. doi: 10.3390/ijms21051651.
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Iron metabolism and iron disorders revisited in the hepcidin era.铁代谢与铁代谢紊乱:在铁调素时代的再认识
Haematologica. 2020 Jan 31;105(2):260-272. doi: 10.3324/haematol.2019.232124. Print 2020.
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Despite Genetic Iron Overload, -Hemochromatosis Mice Do Not Show Bone Loss.尽管存在遗传性铁过载,但β-地中海贫血小鼠并未出现骨质流失。
JBMR Plus. 2019 Jul 26;3(9):e10206. doi: 10.1002/jbm4.10206. eCollection 2019 Sep.
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Mouse models of hereditary hemochromatosis do not develop early liver fibrosis in response to a high fat diet.遗传性血色素沉着症的小鼠模型在高脂肪饮食的刺激下不会发生早期肝纤维化。
PLoS One. 2019 Aug 23;14(8):e0221455. doi: 10.1371/journal.pone.0221455. eCollection 2019.
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Cell Death Dis. 2019 Jun 18;10(6):449. doi: 10.1038/s41419-019-1678-y.