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调节脂质代谢可改善肿瘤免疫治疗

英文原题:Modulating lipid metabolism improves tumor immunotherapy.

查看英文原题

Modulating lipid metabolism improves tumor immunotherapy.

PubMed 2025/02/04(内容时间) J Immunother Cancer Q1 · IF 11.7(JCR 2025)

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中文摘要

免疫治疗在肿瘤治疗中取得了显著进展,然而多种因素影响其疗效。肿瘤中常见的脂质代谢异常可促进肿瘤增殖、侵袭和转移。来自重庆大学附属肿瘤医院肿瘤内科的Li等人构建了脂质代谢评分系统,并报道MK1775抑制肿瘤相关巨噬细胞中的脂肪酸氧化并减少T细胞浸润,进一步增强免疫治疗疗效。该研究证明了脂质代谢评分系统和脂质代谢在免疫治疗中的关键作用。目前,脂肪酸、磷脂和胆固醇等脂质的代谢已被报道可通过调节免疫细胞(包括T细胞、NK 细胞和巨噬细胞)影响肿瘤微环境。这些代谢变化可损害免疫治疗疗效,导致肿瘤进展。因此,脂质代谢成为改善免疫治疗疗效的重要免疫调节因子,并为肿瘤联合治疗提供了新颖而有力的策略。

展开英文摘要原文

Immunotherapy has progressed significantly in cancer treatment; however, several factors influence its outcomes. Abnormal lipid metabolism, which is frequently observed in cancers, promotes tumor proliferation, invasion, and metastasis. Li et al from the Medical Oncology Department of Chongqing University Cancer Hospital constructed a lipid metabolism scoring system and reported that MK1775 inhibited fatty acid oxidation in tumor-associated macrophages and reduced T-cell infiltration, further enhancing the efficacy of immunotherapy.

This study demonstrated the critical role of lipid metabolism scoring system and lipid metabolism in immunotherapy. Currently, the metabolism of lipids, such as fatty acids, phospholipids, and cholesterol, has been reported to affect the tumor microenvironment by regulating immune cells, including T cells, natural killer cells, and macrophages.

These metabolic changes can impair the efficacy of immunotherapy, resulting in tumor progression. Consequently, lipid metabolism emerges as an important immune regulator for improving immunotherapeutic outcomes and provides a novel and powerful strategy for tumor combination therapy.

论文信息

作者
Ping Y、Fan Q、Zhang Y
第一作者单位
Biotherapy Center, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.China
通讯作者单位
Biotherapy Center, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China yizhang@zzu.edu.cn.China
期刊
Journal for immunotherapy of cancer2025 Feb 4
原文标识
PubMed 39904563 · DOI 10.1136/jitc-2024-010824