RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Immunometabolism in lung cancer - The link between metabolism and immune response.
Immunometabolism in lung cancer - The link between metabolism and immune response.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
肺癌仍然是全球癌症相关死亡的主要原因,其特征是肿瘤代谢与免疫逃逸机制之间复杂的相互作用。本综述探讨了免疫代谢这一新兴领域,重点阐述肺肿瘤内的代谢重编程不仅为癌症进展提供能量,还塑造了肿瘤免疫微环境(TME)。关键代谢途径,如糖酵解、谷氨酰胺分解和脂质代谢,在肺癌细胞中发生广泛改变,通过营养竞争、乳酸积累和免疫检查点调节等机制促进免疫抑制。免疫细胞,包括肿瘤相关巨噬细胞(TAMs)、T 细胞、NK 细胞和树突状细胞,由于这些代谢限制而出现功能受损。本综述进一步讨论了靶向免疫代谢途径的治疗策略,包括葡萄糖和氨基酸转运体抑制剂、脂质生物合成酶抑制剂,以及 IDO 和 CD73 等免疫代谢检查点抑制剂。尽管临床前结果令人鼓舞,但代谢可塑性、全身毒性和生物标志物可用性有限等挑战阻碍了临床转化。未来方向强调整合多组学、代谢谱分析和联合免疫治疗,以实现个体化治疗并克服耐药性。深入理解免疫代谢串扰对于推进肺癌精准医学至关重要。
Lung cancer remains a leading cause of cancer-related mortality worldwide, characterized by complex interactions between tumor metabolism and immune evasion mechanisms. This review explores the emerging field of immunometabolism, highlighting how metabolic reprogramming within lung tumors not only fuels cancer progression but also shapes the tumor immune microenvironment (TME). Key metabolic pathways, such as glycolysis, glutaminolysis, and lipid metabolism, are extensively altered in lung cancer cells, facilitating immune suppression through mechanisms such as nutrient competition, lactate accumulation, and modulation of immune checkpoints. Immune cells, including tumor-associated macrophages (TAMs), T cells, NK cells, and dendritic cells, undergo functional impairment due to these metabolic constraints.
The review further discusses therapeutic strategies targeting immunometabolic pathways, including inhibitors of glucose and amino acid transporters, lipid biosynthesis enzymes, and immune-metabolic checkpoints such as IDO and CD73. Despite promising preclinical outcomes, challenges such as metabolic plasticity, systemic toxicity, and limited biomarker availability hinder clinical translation.
Future directions emphasize the integration of multi-omics, metabolic profiling, and combinatory immunotherapy to personalize treatment and overcome resistance. A deeper understanding of immunometabolic crosstalk is pivotal for advancing precision medicine in lung cancer.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
MEMBER ACCOUNT
登录成功会直接打开下一页。