关于 SYK 靶向实体瘤的新见解。
New insights into SYK targeting in solid tumors.
发表日期:2024 Oct
作者:
Shweta Joshi
来源:
TRENDS IN PHARMACOLOGICAL SCIENCES
摘要:
脾酪氨酸激酶 (SYK) 主要在造血细胞中表达,因其在 B 细胞恶性肿瘤和自身免疫性疾病中的关键作用而被广泛研究。在上皮实体瘤中,SYK 表现出矛盾的作用,在某些癌症中充当肿瘤抑制因子,而在另一些癌症中则驱动肿瘤生长。最近的临床前研究已经确定了 SYK 在肿瘤微环境 (TME) 中的作用,揭示了免疫细胞(尤其是 B 细胞和骨髓细胞)中的 SYK 信号传导可促进免疫抑制、肿瘤生长和各种实体瘤的转移。本综述探讨了 SYK 在实体瘤中的新兴作用、SYK 激活机制以及 SYK 抑制剂作为独立治疗或与免疫疗法或化疗联合治疗实体瘤的临床前和临床研究结果。版权所有 © 2024 Elsevier Ltd.保留权利。
Spleen tyrosine kinase (SYK) is predominantly expressed in hematopoietic cells and has been extensively studied for its pivotal role in B cell malignancies and autoimmune diseases. In epithelial solid tumors, SYK shows a paradoxical role, acting as a tumor suppressor in some cancers while driving tumor growth in others. Recent preclinical studies have identified the role of SYK in the tumor microenvironment (TME), revealing that SYK signaling in immune cells, especially B cells, and myeloid cells, promote immunosuppression, tumor growth, and metastasis across various solid tumors. This review explores the emerging roles of SYK in solid tumors, the mechanisms of SYK activation, and findings from preclinical and clinical studies of SYK inhibitors as either standalone treatments or in combination with immunotherapy or chemotherapy for solid tumors.Copyright © 2024 Elsevier Ltd. All rights reserved.