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靶向铁以抑制癌症进展。

Targeting iron to contrast cancer progression.

机构信息

Department of Chemistry and Biochemistry, The University of Arizona, 1306 E. University Blvd., Tucson, AZ 85721-0041, USA.

出版信息

Curr Opin Chem Biol. 2023 Jun;74:102315. doi: 10.1016/j.cbpa.2023.102315. Epub 2023 May 13.

Abstract

An altered metabolism of iron fuels cancer growth, invasion, metastasis, and recurrence. Ongoing research in cancer biology is delineating a complex iron-trafficking program involving both malignant cells and their support network of cancer stem cells, immune cells, and other stromal components in the tumor microenvironment. Iron-binding strategies in anticancer drug discovery are being pursued in clinical trials and in multiple programs at various levels of development. Polypharmacological mechanisms of action, combined with emerging iron-associated biomarkers and companion diagnostics, are poised to offer new therapeutic options. By targeting a fundamental player in cancer progression, iron-binding drug candidates (either alone or in combination therapy) have the potential to impact a broad range of cancer types and to address the major clinical problems of recurrence and resistance to therapy.

摘要

铁代谢的改变为癌症的生长、侵袭、转移和复发提供了燃料。癌症生物学领域的持续研究正在描绘一个涉及恶性细胞及其癌症干细胞支持网络、免疫细胞和肿瘤微环境中其他基质成分的复杂铁运输程序。在临床试验和多个不同开发阶段的项目中,都在进行抗癌药物发现中的铁结合策略。多药理学作用机制,结合新兴的铁相关生物标志物和伴随诊断,有望提供新的治疗选择。通过靶向癌症进展中的一个基本参与者,铁结合候选药物(单独或联合治疗)有可能影响广泛的癌症类型,并解决复发和治疗耐药的主要临床问题。

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