Zhou Xin, Jiang Jinliang, Liu Jingjing, Wang Qinglu, Luo Ying, Wu Liping
Graduate School of Education, Shandong Sport University, Jinan, Shandong, China.
Department of Clinical laboratory, Zibo Central Hospital, Zibo, China.
Front Genet. 2025 Jul 9;16:1620723. doi: 10.3389/fgene.2025.1620723. eCollection 2025.
Cancer, as one of the most deadly and burdensome diseases in the world today, causes irreversible damage to the body. However, due to the ineffective suppression of the inflammatory environment within tumors, identifying new therapeutic targets for cancer treatment has become an urgent issue. Recent studies have shown that lactate, a key product of glycolysis and exercise, is closely related to tumor development. Under normal conditions, lactate regulates various biological functions and can influence immune suppression, thereby interfering with tumor progression. Due to the Warburg effect, lactate levels in the tumor microenvironment (TME) are maintained at high levels. High levels of lactate can further induce the activation of an emerging post-translational modification-lactylation, which enhances the expression of relevant signaling pathways, including JAK-STAT and PI3K/Akt/mTOR. This, in turn, suppresses the body's immune surveillance function and drives tumor progression through epigenetic-metabolic interactions. At the same time, aerobic exercise, as an important intervention for cancer, can enhance anti-inflammatory capacity by secreting muscle factors such as iris protein and tumor suppressor M, and it can also increase the infiltration of immune cells, including CD8 T cells, improving tumor-killing abilities. Based on this, regular aerobic exercise can accelerate the clearance rate of lactate in the body, enhance lactate metabolism, reduce lactate concentration in the TME, and alleviate immune suppression. Therefore, this review explores the mechanisms behind the abnormal elevation of lactate in tumor cells and the occurrence of lactylation, proposing that aerobic exercise can intervene in the tumor process by inhibiting lactylation. The aim is to explore the interaction between aerobic exercise-induced lactylation modification and the tumor microenvironment, identify new therapeutic targets for solid tumors, and provide new ideas for their treatment.
癌症作为当今世界上最致命、负担最重的疾病之一,会对身体造成不可逆转的损害。然而,由于肿瘤内炎症环境的抑制效果不佳,确定癌症治疗的新靶点已成为一个紧迫问题。最近的研究表明,乳酸作为糖酵解和运动的关键产物,与肿瘤发展密切相关。在正常情况下,乳酸调节各种生物学功能,并能影响免疫抑制,从而干扰肿瘤进展。由于瓦伯格效应,肿瘤微环境(TME)中的乳酸水平维持在较高水平。高浓度的乳酸可进一步诱导一种新出现的翻译后修饰——乳酰化的激活,这会增强包括JAK-STAT和PI3K/Akt/mTOR在内的相关信号通路的表达。反过来,这会抑制机体的免疫监视功能,并通过表观遗传-代谢相互作用推动肿瘤进展。同时,有氧运动作为癌症的一种重要干预手段,可通过分泌如鸢尾蛋白和肿瘤抑制因子M等肌肉因子来增强抗炎能力,还能增加包括CD8 T细胞在内的免疫细胞浸润,提高肿瘤杀伤能力。基于此,定期有氧运动可加速体内乳酸的清除率,增强乳酸代谢,降低肿瘤微环境中的乳酸浓度,并减轻免疫抑制。因此,本综述探讨了肿瘤细胞中乳酸异常升高及乳酰化发生背后的机制,提出有氧运动可通过抑制乳酰化来干预肿瘤进程。目的是探索有氧运动诱导的乳酰化修饰与肿瘤微环境之间的相互作用,确定实体瘤的新治疗靶点,并为其治疗提供新思路。