Ahmetoglu Derin, Zheng Haoyi, Swart Aaron, Zhu Hua, Li Ming
Brain Tumor Research Centre of Excellence, Peninsula Medical School, University of Plymouth, Plymouth PL6 8BU, UK.
Department of Neurosurgery, University of Minnesota, Minneapolis, MN 55455, USA.
Int J Mol Sci. 2025 Jun 7;26(12):5477. doi: 10.3390/ijms26125477.
Guanylate-binding proteins (GBPs), encompassing GBP1 through GBP7 in humans, are interferon-inducible large GTPases of the dynamin superfamily, renowned for their pivotal roles in cell-autonomous immunity against intracellular pathogens such as viruses, bacteria, and protozoa. By recognizing pathogen-associated molecular patterns (PAMPs) and danger-associated molecular patterns (DAMPs), GBPs orchestrate lysosomal targeting, regulate inflammatory cascades, and modulate apoptosis to protect host tissues from immune-mediated damage. Beyond their foundational roles in immunity, GBPs exhibit context-dependent effects in human cancer, promoting malignancy in some tumors through enhanced immune signaling, inhibition of apoptosis, and resistance to therapies, or suppressing tumor growth through immune activation and cell cycle regulation. This comprehensive review explores the structural intricacies, immune functions, and multifaceted contributions of human GBPs to cancer, delving into their molecular mechanisms, prognostic potential, and therapeutic implications. We incorporate the latest insights to highlight how understanding GBP regulation could reshape cancer treatment strategies.
鸟苷酸结合蛋白(GBP)在人类中包括GBP1至GBP7,是发动蛋白超家族中干扰素诱导的大型GTP酶,因其在针对病毒、细菌和原生动物等细胞内病原体的细胞自主免疫中发挥关键作用而闻名。通过识别病原体相关分子模式(PAMP)和危险相关分子模式(DAMP),GBP协调溶酶体靶向、调节炎症级联反应并调节细胞凋亡,以保护宿主组织免受免疫介导的损伤。除了在免疫中的基础作用外,GBP在人类癌症中表现出依赖于背景的效应,通过增强免疫信号传导、抑制细胞凋亡和抵抗治疗在某些肿瘤中促进恶性肿瘤,或通过免疫激活和细胞周期调节抑制肿瘤生长。这篇综述全面探讨了人类GBP的结构复杂性、免疫功能及其对癌症的多方面贡献,深入研究了它们的分子机制、预后潜力和治疗意义。我们纳入了最新的见解,以强调了解GBP调节如何重塑癌症治疗策略。