State Key Laboratory of Oral & Maxillofacial Reconstruction and Regeneration, Key Laboratory of Oral Biomedicine Ministry of Education, Hubei Key Laboratory of Stomatology, School & Hospital of Stomatology, Frontier Science Center for Immunology and Metabolism, Taikang Center for Life and Medical Sciences, Wuhan University, Wuhan, China; Department of Stomatology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
State Key Laboratory of Oral & Maxillofacial Reconstruction and Regeneration, Key Laboratory of Oral Biomedicine Ministry of Education, Hubei Key Laboratory of Stomatology, School & Hospital of Stomatology, Frontier Science Center for Immunology and Metabolism, Taikang Center for Life and Medical Sciences, Wuhan University, Wuhan, China.
Int Immunopharmacol. 2024 Dec 25;143(Pt 1):113212. doi: 10.1016/j.intimp.2024.113212. Epub 2024 Sep 30.
Recent advancements in tumor immunotherapy, particularly PD-1 targeted therapy, have shown significant promise, marking major progress in tumor treatment approaches. Despite this, the development of resistance to therapy and mechanisms of immune evasion by tumors pose considerable obstacles to the broad application of immunotherapy. This necessitates a deeper exploration of complex immune signaling pathways integral to tumor immunity. This review aims to critically analyze the role of liquid-liquid phase separation (LLPS) within tumor immunity, specifically its impact on immune signaling pathways and its potential to foster the development of novel cancer therapies. LLPS, a biophysical process newly recognized for its ability to spontaneously segregate and organize biomacromolecules into liquid-like condensates through weak multivalent interactions, offers a novel perspective on the formation of signaling clusters and the functionality of immune molecules. The review delves into the micromolecular mechanisms behind the creation of signaling condensates via LLPS and reviews recent progress in adjusting signaling pathways pertinent to tumor immunity, including the T cell receptor (TCR), B cell receptor (BCR), immune checkpoints, and innate immune pathways such as the cGAS-STING pathway, stress granules, and the ADP-heptose-ALPK1 signaling axis. Furthermore, it considers the prospects of utilizing LLPS to generate groundbreaking cancer therapies capable of navigating past current treatment barriers. Through an extensive examination of LLPS's impact on tumor immunity, the review seeks to highlight novel therapeutic strategies and address the challenges and future directions in this rapidly evolving field.
近年来,肿瘤免疫疗法,特别是 PD-1 靶向疗法取得了显著进展,为肿瘤治疗方法带来了重大突破。尽管如此,肿瘤对治疗的耐药性发展和免疫逃逸机制仍然是免疫治疗广泛应用的重大障碍。这需要更深入地探索与肿瘤免疫相关的复杂免疫信号通路。
本综述旨在批判性地分析液-液相分离(LLPS)在肿瘤免疫中的作用,特别是其对免疫信号通路的影响及其在促进新型癌症治疗方法发展方面的潜力。液-液相分离是一种新发现的生物物理过程,通过弱多价相互作用能够自发地将生物大分子分离并组织成类似液体的凝聚物,为信号簇的形成和免疫分子的功能提供了新的视角。
本综述深入探讨了通过 LLPS 形成信号凝聚物的微观分子机制,并回顾了最近在调节与肿瘤免疫相关的信号通路方面的进展,包括 T 细胞受体(TCR)、B 细胞受体(BCR)、免疫检查点以及先天免疫途径,如 cGAS-STING 途径、应激颗粒和 ADP-己糖-ALPK1 信号轴。此外,还考虑了利用 LLPS 产生能够克服当前治疗障碍的突破性癌症治疗方法的前景。
通过对 LLPS 对肿瘤免疫影响的广泛研究,本综述旨在强调新的治疗策略,并探讨这一快速发展领域面临的挑战和未来方向。