Li Jiamu, Li Xinqiao, Hu Jinpeng, You Zinan, Jing Zhitao
Department of Neurosurgery, The First Hospital of China Medical University, Nanjing Street 155, Heping District, Shenyang 110001, PR China.
Department of Neurosurgery, The First Hospital of China Medical University, Nanjing Street 155, Heping District, Shenyang 110001, PR China; Department of Neurosurgery, Liaoning Cancer Hospital and Institute, Cancer Hospital of China Medical University, Shenyang 110042, PR China.
Biochim Biophys Acta Rev Cancer. 2025 Oct;1880(5):189436. doi: 10.1016/j.bbcan.2025.189436. Epub 2025 Sep 4.
The complement system, a cornerstone of innate immunity, plays pivotal roles in both defense and pathology, particularly through its anaphylatoxins, C3a and C5a. These small peptides, generated during complement activation, not only mediate pro-inflammatory responses but also contribute to the progression of various cancers by modulating the tumor microenvironment (TME). Anaphylatoxins influence tumor cell proliferation, epithelial-mesenchymal transition, angiogenesis, immune suppression, and therapy resistance via key signaling pathways such as PI3K/AKT, MEK/ERK, and p38 MAPK. This review summarizes recent findings on the roles of C3a and C5a in different tumor types, including glioma, lung cancer, melanoma, breast cancer, and hematological malignancies, highlighting their potential as biomarkers and therapeutic targets. Additionally, we discuss the development of anaphylatoxin inhibitors, their clinical applications, and the synergistic effects of combining these inhibitors with immune checkpoint blockade therapies. A deeper understanding of anaphylatoxin-mediated mechanisms may provide novel strategies for cancer diagnosis, prognosis, and treatment, paving the way for targeted and combination therapies to overcome tumor progression and immune evasion.
补体系统作为固有免疫的基石,在防御和病理过程中均发挥着关键作用,尤其是通过其过敏毒素C3a和C5a。这些在补体激活过程中产生的小肽,不仅介导促炎反应,还通过调节肿瘤微环境(TME)促进各种癌症的进展。过敏毒素通过PI3K/AKT、MEK/ERK和p38 MAPK等关键信号通路影响肿瘤细胞增殖、上皮-间质转化、血管生成、免疫抑制和治疗抗性。本综述总结了C3a和C5a在不同肿瘤类型(包括神经胶质瘤、肺癌、黑色素瘤、乳腺癌和血液系统恶性肿瘤)中作用的最新研究结果,强调了它们作为生物标志物和治疗靶点的潜力。此外,我们还讨论了过敏毒素抑制剂的研发、它们的临床应用以及将这些抑制剂与免疫检查点阻断疗法联合使用的协同效应。对过敏毒素介导机制的更深入理解可能为癌症诊断、预后和治疗提供新策略,为克服肿瘤进展和免疫逃逸的靶向及联合疗法铺平道路。