V. N. Blindar, G. N. Zubrikhina, T. V. Davydova, M. M. Dobrovolskaya
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引用次数: 0
摘要
背景。铁的获取、流出、储存和调控途径在癌症中被破坏,这表明铁代谢的重编程是肿瘤细胞存活的核心方面之一。的目标。综述了hepcidin、铁转运蛋白调控肿瘤患者铁代谢的现代文献资料,并展望了对肿瘤患者铁代谢的纠正。材料与方法。本文介绍了国内外对癌症患者铁代谢特性的研究结果及其校正的前景。在1988-2023年的web of Science、PubMed、Medline、elibrar .ru系统中搜索相关来源。在分析的研究中,最相关的61项研究被用于撰写系统综述。结果。在过去的十年中,人们对蛋白质的作用有了新的认识,特别是hepcidin和铁转运蛋白,它们调节细胞铁在癌症生长、血管生成和转移中的作用。hepcidin修饰策略和低氧诱导因子稳定剂的新治疗方法正在出现,但其治疗癌症患者铁代谢的效果需要评估和临床试验。结论。通过对文献资料的分析,发现hepcidin和铁转运蛋白在癌症患者中的调控研究具有较高的相关性,需要进一步研究。
Features of regulation of hepcidin and ferroportin in cancer patients (literary review)
Background. The pathways of iron acquisition, outflow, storage and regulation are disrupted in cancer, which suggests that the reprogramming of iron metabolism is one of the central aspects of the survival of tumor cells. Aim. Is to review and generalize modern literature data on the regulation of hepcidin, ferroportin and prospects for the correction of iron metabolism in cancer patients. Materials and Methods. The paper presents the results of international and domestic studies of the peculiarities of iron metabolism and the prospects for its correction in cancer patients. The search for relevant sources was carried out in the web of Science, PubMed, Medline, eLibrary.ru systems for 1988–2023. Of the analyzed studies 61, the most relevant, were used to write a systematic review. Results . Over the past decade, a new understanding has emerged of the role of proteins, in particular hepcidin and ferroportin, which regulate cellular iron in cancer growth, angiogenesis and metastasis. New treatment methods with hepcidin-modifying strategies and stabilizers of hypoxia-induced factors are emerging, but their therapeutic efficacy for correcting iron metabolism in cancer patients needs to be evaluated and clinical trials. Conclusion. Analysis of the literature data has shown the high relevance of studies of the regulation of hepcidin and ferroportin in cancer patients and the need for further study of this problem.