Institute of Natural Medicine, University of Toyama, Toyama 930-0194, Japan.
Faculty of Pharmacy, Universitas Gadjah Mada, Yogyakarta 55281, Indonesia.
Int J Mol Sci. 2024 May 13;25(10):5288. doi: 10.3390/ijms25105288.
Cancer cells adeptly manipulate their metabolic processes to evade immune detection, a phenomenon intensifying the complexity of cancer progression and therapy. This review delves into the critical role of cancer cell metabolism in the immune-editing landscape, highlighting how metabolic reprogramming facilitates tumor cells to thrive despite immune surveillance pressures. We explore the dynamic interactions within the tumor microenvironment (TME), where cancer cells not only accelerate their glucose and amino acid metabolism but also induce an immunosuppressive state that hampers effective immune response. Recent findings underscore the metabolic competition between tumor and immune cells, particularly focusing on how this interaction influences the efficacy of emerging immunotherapies. By integrating cutting-edge research on the metabolic pathways of cancer cells, such as the Warburg effect and glutamine addiction, we shed light on potential therapeutic targets. The review proposes that disrupting these metabolic pathways could enhance the response to immunotherapy, offering a dual-pronged strategy to combat tumor growth and immune evasion.
癌细胞巧妙地操纵其代谢过程以逃避免疫检测,这种现象加剧了癌症进展和治疗的复杂性。本综述深入探讨了癌细胞代谢在免疫编辑景观中的关键作用,强调了代谢重编程如何使肿瘤细胞在免疫监视压力下茁壮成长。我们探讨了肿瘤微环境 (TME) 内的动态相互作用,其中癌细胞不仅加速葡萄糖和氨基酸代谢,还诱导抑制性免疫状态,从而阻碍有效的免疫反应。最近的研究结果强调了肿瘤细胞和免疫细胞之间的代谢竞争,特别是关注这种相互作用如何影响新兴免疫疗法的疗效。通过整合癌细胞代谢途径的最新研究,如瓦博格效应和谷氨酰胺成瘾,我们揭示了潜在的治疗靶点。该综述提出,破坏这些代谢途径可以增强对免疫疗法的反应,提供一种双重策略来对抗肿瘤生长和免疫逃避。