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肝细胞癌中的铁死亡:从机制到影响

Ferroptosis in hepatocellular carcinoma, from mechanism to effect.

作者信息

Jiang Shuang, Zhang Guangcong, Ma Yanan, Wu Dongyu, Xie Da, Zhou Songke, Jiang Xuemei

机构信息

Department of Gastroenterology, Hainan General Hospital (Affiliated Hainan Hospital of Hainan Medical University), Haikou, China.

Department of Gastroenterology and Hepatology, Zhongshan Hospital of Fudan University, Shanghai, China.

出版信息

Front Oncol. 2024 Mar 5;14:1350011. doi: 10.3389/fonc.2024.1350011. eCollection 2024.


DOI:10.3389/fonc.2024.1350011
PMID:38511140
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10952836/
Abstract

Hepatocellular carcinoma (HCC) is a prevalent malignant tumor worldwide, characterized by high malignancy and rapid progression. Most cases are diagnosed at intermediate to advanced stages. Current treatment methods have limited efficacy, resulting in high recurrence rates and poor prognosis. Radical hepatectomy remains the primary treatment for HCC, complemented by radiotherapy, chemotherapy, targeted therapy, and immunotherapy. Despite significant improvement in patient prognosis with radical hepatectomy, the five-year survival rate post-surgery remains low; thus necessitating exploration of more effective therapeutic approaches. Ferroptosis is a recently discovered form of cell death that can modulate the occurrence and development of HCC through various mechanisms. This article aims to elucidate the mechanism of ferroptosis and its impact on HCC development to provide novel insights for diagnosis and treatment.

摘要

肝细胞癌(HCC)是一种在全球范围内普遍存在的恶性肿瘤,具有高恶性和快速进展的特点。大多数病例在中晚期被诊断出来。目前的治疗方法疗效有限,导致复发率高且预后不良。根治性肝切除术仍然是HCC的主要治疗方法,辅以放疗、化疗、靶向治疗和免疫治疗。尽管根治性肝切除术使患者预后有了显著改善,但术后五年生存率仍然很低;因此有必要探索更有效的治疗方法。铁死亡是最近发现的一种细胞死亡形式,它可以通过多种机制调节HCC的发生和发展。本文旨在阐明铁死亡的机制及其对HCC发展的影响,为诊断和治疗提供新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8cf8/10952836/e013fd1277c3/fonc-14-1350011-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8cf8/10952836/e013fd1277c3/fonc-14-1350011-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8cf8/10952836/e013fd1277c3/fonc-14-1350011-g001.jpg

相似文献

[1]
Ferroptosis in hepatocellular carcinoma, from mechanism to effect.

Front Oncol. 2024-3-5

[2]
Ferroptosis: From Basic Research to Clinical Therapeutics in Hepatocellular Carcinoma.

J Clin Transl Hepatol. 2023-2-28

[3]
Breaking the Barriers of Therapy Resistance: Harnessing Ferroptosis for Effective Hepatocellular Carcinoma Therapy.

J Hepatocell Carcinoma. 2024-7-2

[4]
Ferroptosis Suppressor Protein 1 Inhibition Promotes Tumor Ferroptosis and Anti-tumor Immune Responses in Liver Cancer.

Cell Mol Gastroenterol Hepatol. 2023

[5]
Parthenolide induces rapid thiol oxidation that leads to ferroptosis in hepatocellular carcinoma cells.

Front Toxicol. 2022-12-14

[6]
From synergy to resistance: Navigating the complex relationship between sorafenib and ferroptosis in hepatocellular carcinoma.

Biomed Pharmacother. 2024-1

[7]
A Novel Ferroptosis-Related Signature for Prediction of Prognosis, Immune Profiles and Drug Sensitivity in Hepatocellular Carcinoma Patients.

Curr Oncol. 2022-9-27

[8]
Ferroptosis in Hepatocellular Carcinoma: Mechanisms, Drug Targets and Approaches to Clinical Translation.

Cancers (Basel). 2022-4-4

[9]
Comprehensive characterization of ferroptosis in hepatocellular carcinoma revealing the association with prognosis and tumor immune microenvironment.

Front Oncol. 2023-3-27

[10]
Construction and Validation of a Ferroptosis-Related lncRNA Signature as a Novel Biomarker for Prognosis, Immunotherapy and Targeted Therapy in Hepatocellular Carcinoma.

Front Cell Dev Biol. 2022-2-22

本文引用的文献

[1]
Tumor-specific GPX4 degradation enhances ferroptosis-initiated antitumor immune response in mouse models of pancreatic cancer.

Sci Transl Med. 2023-11

[2]
PGAM1 Inhibition Promotes HCC Ferroptosis and Synergizes with Anti-PD-1 Immunotherapy.

Adv Sci (Weinh). 2023-10

[3]
Donafenib and GSK-J4 Synergistically Induce Ferroptosis in Liver Cancer by Upregulating HMOX1 Expression.

Adv Sci (Weinh). 2023-8

[4]
The Warburg effect modulates DHODH role in ferroptosis: a review.

Cell Commun Signal. 2023-5-5

[5]
Corrigendum: CCDC25 may be a potential diagnostic and prognostic marker of hepatocellular carcinoma: Results from microarray analysis.

Front Surg. 2023-3-28

[6]
ATF4 suppresses hepatocarcinogenesis by inducing SLC7A11 (xCT) to block stress-related ferroptosis.

J Hepatol. 2023-8

[7]
DDTC-Cu(I) based metal-organic framework (MOF) for targeted melanoma therapy by inducing SLC7A11/GPX4-mediated ferroptosis.

Colloids Surf B Biointerfaces. 2023-5

[8]
Fe-MnO nanosheets loading dihydroartemisinin for ferroptosis and immunotherapy.

Biomed Pharmacother. 2023-5

[9]
Combining ferroptosis induction with MDSC blockade renders primary tumours and metastases in liver sensitive to immune checkpoint blockade.

Gut. 2023-9

[10]
Sodium Butyrate Induces CRC Cell Ferroptosis via the CD44/SLC7A11 Pathway and Exhibits a Synergistic Therapeutic Effect with Erastin.

Cancers (Basel). 2023-1-9

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