Zhang Xue, Chen Dong-Bo, Zhang Rui, Chen Pu, She Shao-Ping, Yang Yao, Ren Li-Ying, Chen Hong-Song
Peking University People's Hospital, Peking University Hepatology Institute, Infectious Disease and Hepatology Center of Peking University People's Hospital, Beijing Key Laboratory of Hepatitis C and Immunotherapy for Liver Diseases, Beijing International Cooperation Base for Science and Technology on NAFLD Diagnosis, Peking University People's Hospital, Beijing 100044, China.
Department of Anesthesiology, Peking University Third Hospital, Beijing 100191, China.
World J Gastrointest Oncol. 2025 Sep 15;17(9):109824. doi: 10.4251/wjgo.v17.i9.109824.
Hepatocellular carcinoma (HCC) is a primary malignant tumor of the liver and one of the most common malignant tumors, as well as the third leading cause of cancer-related death. In recent years, immune checkpoint inhibitors have emerged as a key strategy in cancer treatment. However, anti-programmed cell death 1/programmed death ligand 1 therapies, one of the main immunotherapeutic approaches, only elicit a response in only approximately 20% of advanced HCC. This suggests that there may be other immune checkpoints playing important roles in HCC immunotherapy. Recent studies have highlighted Signal regulatory protein alpha (SIRPα) is a phagocytic checkpoint in macrophages and other immune cells, as a promising novel therapeutic target in tumor immunotherapy. This review summarizes current progress on SIRPα in HCC and identifies key challenges for future related research.
肝细胞癌(HCC)是肝脏的原发性恶性肿瘤,也是最常见的恶性肿瘤之一,并且是癌症相关死亡的第三大主要原因。近年来,免疫检查点抑制剂已成为癌症治疗的关键策略。然而,抗程序性细胞死亡蛋白1/程序性死亡配体1疗法作为主要的免疫治疗方法之一,仅在约20%的晚期HCC患者中引发反应。这表明可能存在其他免疫检查点在HCC免疫治疗中发挥重要作用。最近的研究强调,信号调节蛋白α(SIRPα)是巨噬细胞和其他免疫细胞中的吞噬检查点,是肿瘤免疫治疗中有前景的新型治疗靶点。本综述总结了HCC中SIRPα的当前进展,并确定了未来相关研究的关键挑战。