利用癌症中的核苷酸代谢和免疫:肿瘤微环境视角。

Hadil Sulieman, Alexandra Emerson, Peter M Wilson, Karl A Mulligan, Robert D Ladner, Melissa J LaBonte
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摘要

肿瘤微环境(TME)是癌细胞新陈代谢和免疫系统复杂交汇的动态连接点,其中核苷酸代谢(NM)发挥着关键作用。本综述探讨了核苷酸代谢在癌细胞增殖中的关键功能及其对 TME 和免疫环境的深远影响。NM 是 DNA 和 RNA 合成的必要条件,在癌细胞中明显上调,以满足快速生长的需求。这种新陈代谢的重新布线助长了癌症的发展,同时也塑造了 TME,影响了免疫细胞的功能和活力。TME中改变的核苷酸环境会抑制免疫反应,帮助癌细胞逃避免疫监视。核苷酸领域的药物发现揭示了不同的治疗策略,包括核苷酸合成抑制剂和靶向挽救途径的药物,本综述将对此进行深入讨论。此外,本综述还强调了新出现的将 NM 靶向疗法与免疫疗法相结合的策略,特别是这些疗法在使肿瘤对免疫检查点抑制剂敏感和提高整体疗效方面的作用。人类基因组计划为个性化医疗铺平了道路,与既有的 "一刀切 "癌症治疗方法形成了鲜明对比。对TME和NM认识的进步激发了人们对个性化治疗策略的兴趣。本综述强调了利用个体肿瘤代谢特征指导治疗选择的潜力,旨在优化疗效并减少不良反应。在癌症治疗中靶向 NM 的战略重要性及其与免疫疗法的协同潜力为更有效的个性化癌症治疗提供了一条途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Harnessing nucleotide metabolism and immunity in cancer: a tumour microenvironment perspective.

The tumour microenvironment (TME) is a dynamic nexus where cancer cell metabolism and the immune system intricately converge, with nucleotide metabolism (NM) playing a pivotal role. This review explores the critical function of NM in cancer cell proliferation and its profound influence on the TME and immune landscape. NM is essential for DNA and RNA synthesis and is markedly upregulated in cancer cells to meet the demands of rapid growth. This metabolic rewiring fuels cancer progression, but also shapes the TME, impacting the function and viability of immune cells. The altered nucleotide milieu in the TME can suppress immune response, aiding cancer cell evasion from immune surveillance. Drug discoveries in the field of NM have revealed different therapeutic strategies, including inhibitors of nucleotide synthesis and drugs targeting salvage pathways, which are discussed thoroughly in this review. Furthermore, the emerging strategy of combining NM-targeted therapies with immunotherapies is emphasised, particularly their effect on sensitising tumours to immune checkpoint inhibitors and enhancing overall treatment efficacy. The Human Genome Project paved the way for personalised medicine, countering the established 'one size fits all' approach to cancer treatment. Advances in understanding the TME and NM have spurred interest in personalised therapeutic strategies. This review highlights the potential of leveraging individual tumour metabolic profiles to guide treatment selection, aiming to optimise efficacy and minimise adverse effects. The strategic importance of targeting NM in cancer therapy and its synergistic potential with immunotherapies offers a path towards more effective and personalised cancer treatments.

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