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结直肠癌中铁死亡的研究进展。

Research progress on ferroptosis in colorectal cancer.

机构信息

Central Laboratory, Yanbian University Hospital & Key Laboratory of Pathobiology, Yanbian University, State Ethnic Affairs Commission, Yanbian University, Yanji, China.

Department of Pathology & Cancer Research Center, Yanbian University, Yanji, China.

出版信息

Front Immunol. 2024 Sep 18;15:1462505. doi: 10.3389/fimmu.2024.1462505. eCollection 2024.

DOI:10.3389/fimmu.2024.1462505
PMID:39359721
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11444962/
Abstract

Ferroptosis is a new form of cell death that differs from traditional forms of death. It is ferroptosis-dependent lipid peroxidation death. Colorectal cancer(CRC) is the most common tumor in the gastrointestinal tract with a long occultation period and a poor five-year prognosis. Exploring effective systemic treatments for CRC remains a great challenge worldwide. Numerous studies have demonstrated that ferroptosis can participate in the biological malignant process of various tumor, including CRC, so understanding the role and regulatory mechanisms of ferroptosis in CRC plays a crucial role in the treatment of CRC. In this paper, we reviews the mechanisms of ferroptosis in CRC, the associated regulatory factors and their interactions with various immune cells in the immune microenvironment. In addition, targeting ferroptosis has emerged as an encouraging strategy for CRC treatment. Finally, to inform subsequent research and clinical diagnosis and treatment, we review therapeutic approaches to CRC radiotherapy, immunotherapy, and herbal therapy targeting ferroptosis.

摘要

铁死亡是一种不同于传统死亡形式的新型细胞死亡方式。它是依赖于铁死亡的脂质过氧化死亡。结直肠癌(CRC)是胃肠道最常见的肿瘤,具有较长的隐匿期和较差的五年预后。探索有效的结直肠癌系统治疗方法仍然是全世界面临的巨大挑战。大量研究表明,铁死亡可以参与包括 CRC 在内的各种肿瘤的生物学恶性过程,因此了解铁死亡在 CRC 中的作用和调节机制对于 CRC 的治疗至关重要。在本文中,我们综述了结直肠癌中铁死亡的机制、相关调节因子及其与免疫微环境中各种免疫细胞的相互作用。此外,靶向铁死亡已成为 CRC 治疗的一种有前途的策略。最后,为了为后续的研究和临床诊断和治疗提供信息,我们综述了针对铁死亡的 CRC 放疗、免疫疗法和草药疗法的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cf7/11444962/ed91f043b104/fimmu-15-1462505-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cf7/11444962/2065b0fff111/fimmu-15-1462505-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cf7/11444962/ed91f043b104/fimmu-15-1462505-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cf7/11444962/2065b0fff111/fimmu-15-1462505-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cf7/11444962/ed91f043b104/fimmu-15-1462505-g002.jpg

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Research progress on ferroptosis in colorectal cancer.结直肠癌中铁死亡的研究进展。
Front Immunol. 2024 Sep 18;15:1462505. doi: 10.3389/fimmu.2024.1462505. eCollection 2024.
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Naunyn Schmiedebergs Arch Pharmacol. 2025 Jul 8. doi: 10.1007/s00210-025-04423-1.
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Theranostic Applications of Taurine-Derived Carbon Dots in Colorectal Cancer: Ferroptosis Induction and Multifaceted Antitumor Mechanisms.

本文引用的文献

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A novel antitumor mechanism of triptonide in colorectal cancer: inducing ferroptosis via the SLC7A11/GPX4 axis.三氧化二砷诱导结直肠癌细胞铁死亡的新机制:通过 SLC7A11/GPX4 轴。
Funct Integr Genomics. 2024 Jul 16;24(4):126. doi: 10.1007/s10142-024-01402-2.
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The application of graphene oxide and ferroptosis in the diagnosis and treatment of colorectal cancer: a narrative review.氧化石墨烯与铁死亡在结直肠癌诊断与治疗中的应用:一篇叙述性综述
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Circular RNAs in EMT-driven metastasis regulation: modulation of cancer cell plasticity, tumorigenesis and therapy resistance.
牛磺酸衍生碳点在结直肠癌中的诊疗应用:铁死亡诱导及多方面抗肿瘤机制
Int J Nanomedicine. 2025 Jun 16;20:7613-7635. doi: 10.2147/IJN.S516926. eCollection 2025.
4
Dual-Functional Silicon-Based Nanofluorescent Platform for Iron Detection and Capecitabine Delivery in Colorectal Cancer Treatment.用于结直肠癌治疗中铁检测和卡培他滨递送的双功能硅基纳米荧光平台。
J Fluoresc. 2025 Mar 21. doi: 10.1007/s10895-025-04252-8.
环状 RNA 在 EMT 驱动的转移调控中的作用:调节癌细胞可塑性、肿瘤发生和治疗抵抗。
Cell Mol Life Sci. 2024 May 11;81(1):214. doi: 10.1007/s00018-024-05236-w.
4
Emodin induces ferroptosis in colorectal cancer through NCOA4-mediated ferritinophagy and NF-κb pathway inactivation.大黄素通过 NCOA4 介导的铁蛋白自噬和 NF-κb 通路失活诱导结直肠癌细胞发生铁死亡。
Apoptosis. 2024 Oct;29(9-10):1810-1823. doi: 10.1007/s10495-024-01973-2. Epub 2024 May 5.
5
Baicalein triggers ferroptosis in colorectal cancer cells via blocking the JAK2/STAT3/GPX4 axis.黄芩素通过阻断 JAK2/STAT3/GPX4 轴诱导结直肠癌细胞发生铁死亡。
Acta Pharmacol Sin. 2024 Aug;45(8):1715-1726. doi: 10.1038/s41401-024-01258-z. Epub 2024 Apr 29.
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Ginsenoside compound K induces ferroptosis via the FOXO pathway in liver cancer cells.人参皂苷化合物 K 通过 FOXO 通路诱导肝癌细胞发生铁死亡。
BMC Complement Med Ther. 2024 Apr 25;24(1):174. doi: 10.1186/s12906-024-04471-9.
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Deciphering the molecular and clinical characteristics of TREM2, HCST, and TYROBP in cancer immunity: A comprehensive pan-cancer study.解析癌症免疫中TREM2、HCST和TYROBP的分子及临床特征:一项全面的泛癌研究。
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