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铁死亡:肝癌治疗的新靶点。

Ferroptosis: a new promising target for hepatocellular carcinoma therapy.

机构信息

Department of Clinical Pharmacology, Key Laboratory of Clinical Cancer Pharmacology and Toxicology Research of Zhejiang Province, Affiliated Hangzhou First People's Hospital, Cancer Center, Westlake University School of Medical, Hangzhou, 310006, China.

Fourth Clinical Medical College of Zhejiang, Chinese Medical University, Hangzhou, 310051, China.

出版信息

Mol Cell Biochem. 2024 Oct;479(10):2615-2636. doi: 10.1007/s11010-023-04893-y. Epub 2023 Dec 5.


DOI:10.1007/s11010-023-04893-y
PMID:38051404
Abstract

Hepatocellular carcinoma (HCC) is the sixed most common malignant tumor in the world. The study for HCC is mired in the predicament confronted with the difficulty of early diagnosis and high drug resistance, the survival rate of patients with HCC being low. Ferroptosis, an iron-dependent cell death, has been discovered in recent years as a cell death means with tremendous potential to fight against cancer. The in-depth researches for iron metabolism, lipid peroxidation and dysregulation of antioxidant defense have brought about tangible progress in the firmament of ferroptosis with more and more results showing close connections between ferroptosis and HCC. The potential role of ferroptosis has been widely used in chemotherapy, immunotherapy, radiotherapy, and nanotherapy, with the development of various new drugs significantly improving the prognosis of patients. Based on the characteristics and mechanisms of ferroptosis, this article further focuses on the main signaling pathways and promising treatments of HCC, envisioning that existing problems in regard with ferroptosis and HCC could be grappled with in the foreseeable future.

摘要

肝细胞癌(HCC)是世界上第六种最常见的恶性肿瘤。HCC 的研究陷入了早期诊断困难和药物耐药性高的困境,HCC 患者的生存率较低。近年来,铁依赖性细胞死亡铁死亡作为一种具有巨大抗癌潜力的细胞死亡方式被发现。对铁代谢、脂质过氧化和抗氧化防御失调的深入研究,使铁死亡领域取得了实质性的进展,越来越多的研究结果表明铁死亡与 HCC 密切相关。铁死亡的潜在作用已广泛应用于化疗、免疫治疗、放疗和纳米治疗,各种新药的发展显著改善了患者的预后。基于铁死亡的特点和机制,本文进一步聚焦于 HCC 的主要信号通路和有前途的治疗方法,预计在可预见的未来,现有的铁死亡和 HCC 问题将得到解决。

相似文献

[1]
Ferroptosis: a new promising target for hepatocellular carcinoma therapy.

Mol Cell Biochem. 2024-10

[2]
Benja-ummarit induces ferroptosis with cell ballooning feature through ROS and iron-dependent pathway in hepatocellular carcinoma.

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[3]
Role of ferroptosis in hepatocellular carcinoma.

J Cancer Res Clin Oncol. 2018-8-22

[4]
Current Progress of Ferroptosis Study in Hepatocellular Carcinoma.

Int J Biol Sci. 2024

[5]
Low-density lipoprotein docosahexaenoic acid nanoparticles induce ferroptotic cell death in hepatocellular carcinoma.

Free Radic Biol Med. 2017-9-8

[6]
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Hepatol Int. 2024-2

[7]
Iron accumulation and lipid peroxidation: implication of ferroptosis in hepatocellular carcinoma.

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[8]
DDX39B protects against sorafenib-induced ferroptosis by facilitating the splicing and cytoplasmic export of GPX4 pre-mRNA in hepatocellular carcinoma.

Biochem Pharmacol. 2024-7

[9]
Glycyrrhizic acid attenuates sorafenib resistance by inducing ferroptosis via targeting mTOR signaling in hepatocellular carcinoma.

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[10]
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引用本文的文献

[1]
CD155 promotes the advancement of hepatocellular carcinoma by suppressing the p53-mediated ferroptosis via interacting with CD96.

J Mol Med (Berl). 2025-3

[2]
A Dual-Targeting Biomimetic Nanoplatform Integrates SDT/CDT/Gas Therapy to Boost Synergistic Ferroptosis for Orthotopic Hepatocellular Carcinoma Therapy.

Adv Sci (Weinh). 2025-2

[3]
Semaglutide restores astrocyte-vascular interactions and blood-brain barrier integrity in a model of diet-induced metabolic syndrome.

Diabetol Metab Syndr. 2025-1-4

[4]
[Ferroptosis inducer Erastin inhibits proliferation of liver cancer cells by downregulating ACSL4].

Nan Fang Yi Ke Da Xue Xue Bao. 2024-11-20

[5]
Integrated multiomics analysis identified comprehensive crosstalk between diverse programmed cell death patterns and novel molecular subtypes in Hepatocellular Carcinoma.

Sci Rep. 2024-11-11

[6]
Pharmacologically Targeting Ferroptosis and Cuproptosis in Neuroblastoma.

Mol Neurobiol. 2025-3

[7]
The multifaceted perspectives on the regulation of lncRNAs in hepatocellular carcinoma ferroptosis: from bench-to-bedside.

Clin Exp Med. 2024-7-3

[8]
Pharmacological therapy of metabolic dysfunction-associated steatotic liver disease-driven hepatocellular carcinoma.

Front Pharmacol. 2024-1-19

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