多发性骨髓瘤:信号通路与靶向治疗。
Multiple myeloma: signaling pathways and targeted therapy.
机构信息
Department of Biotherapy, State Key Laboratory of Biotherapy and Cancer Center, Research Unit of Gene and Immunotherapy, Chinese Academy of Medical Sciences, Collaborative Innovation Center of Biotherapy, West China Hospital, Sichuan University, Chengdu, 610041, China.
College of Veterinary Medicine, Shaanxi Center of Stem Cells Engineering and Technology, Northwest A&F University, Yangling, 712100, China.
出版信息
Mol Biomed. 2024 Jul 4;5(1):25. doi: 10.1186/s43556-024-00188-w.
Multiple myeloma (MM) is the second most common hematological malignancy of plasma cells, characterized by osteolytic bone lesions, anemia, hypercalcemia, renal failure, and the accumulation of malignant plasma cells. The pathogenesis of MM involves the interaction between MM cells and the bone marrow microenvironment through soluble cytokines and cell adhesion molecules, which activate various signaling pathways such as PI3K/AKT/mTOR, RAS/MAPK, JAK/STAT, Wnt/β-catenin, and NF-κB pathways. Aberrant activation of these pathways contributes to the proliferation, survival, migration, and drug resistance of myeloma cells, making them attractive targets for therapeutic intervention. Currently, approved drugs targeting these signaling pathways in MM are limited, with many inhibitors and inducers still in preclinical or clinical research stages. Therapeutic options for MM include non-targeted drugs like alkylating agents, corticosteroids, immunomodulatory drugs, proteasome inhibitors, and histone deacetylase inhibitors. Additionally, targeted drugs such as monoclonal antibodies, chimeric antigen receptor T cells, bispecific T-cell engagers, and bispecific antibodies are being used in MM treatment. Despite significant advancements in MM treatment, the disease remains incurable, emphasizing the need for the development of novel or combined targeted therapies based on emerging theoretical knowledge, technologies, and platforms. In this review, we highlight the key role of signaling pathways in the malignant progression and treatment of MM, exploring advances in targeted therapy and potential treatments to offer further insights for improving MM management and outcomes.
多发性骨髓瘤(MM)是第二常见的浆细胞血液恶性肿瘤,其特征是溶骨性骨病变、贫血、高钙血症、肾衰竭和恶性浆细胞的积累。MM 的发病机制涉及 MM 细胞与骨髓微环境通过可溶性细胞因子和细胞黏附分子的相互作用,激活各种信号通路,如 PI3K/AKT/mTOR、RAS/MAPK、JAK/STAT、Wnt/β-catenin 和 NF-κB 通路。这些通路的异常激活导致骨髓瘤细胞的增殖、存活、迁移和耐药性,使其成为治疗干预的有吸引力的靶点。目前,针对 MM 中这些信号通路的批准药物有限,许多抑制剂和激动剂仍处于临床前或临床研究阶段。MM 的治疗选择包括非靶向药物,如烷化剂、皮质类固醇、免疫调节剂、蛋白酶体抑制剂和组蛋白去乙酰化酶抑制剂。此外,针对 MM 的治疗还使用靶向药物,如单克隆抗体、嵌合抗原受体 T 细胞、双特异性 T 细胞衔接器和双特异性抗体。尽管 MM 的治疗取得了重大进展,但该疾病仍然无法治愈,这强调了需要根据新兴的理论知识、技术和平台开发新的或联合的靶向治疗。在这篇综述中,我们强调了信号通路在 MM 的恶性进展和治疗中的关键作用,探讨了靶向治疗的进展和潜在的治疗方法,为改善 MM 的管理和结果提供了进一步的见解。