Journal of Capital Medical University ›› 2025, Vol. 46 ›› Issue (3): 436-441.doi: 10.3969/j.issn.1006-7795.2025.03.006

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B cell receptor signaling pathway and its therapeutic implications in B-cell lymphoma

Wang Jingwen, Li Zhenjun, Lyu Liangcheng, Yao Xiaoyu, Ding Ning*   

  1. Laboratory of Lymphoma Translational Research, Peking University Cancer Hospital & Institute, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Beijing 100142, China
  • Received:2025-02-26 Online:2025-06-21 Published:2025-06-25
  • Supported by:
    This study was supported by National Natural Science Foundation of China (82470178, 81970179),  Natural Science Foundation of Beijing(Z220023), Science Foundation of Peking University Cancer Hospital (JC202401).

Abstract: B-cell lymphomas account for 70%-80% of non-Hodgkin lymphomas(NHL) and exhibit significant heterogeneity in genetic profiles, phenotypic characteristics, and clinical manifestations, posing substantial challenges for clinical management. The B-cell receptor (BCR) is a transmembrane receptor on the surface of B cells that plays a central regulatory role in B-cell development, activation, and adaptive immune responses. As a core mechanism driving malignant transformation in various B-cell malignancies, aberrant activation of the BCR signaling pathway, plays a pivotal role in B lymphoma pathogenesis. Dysregulated BCR signaling not only promotes tumor cell proliferation, survival, and anti-apoptotic capacity but also accelerates malignant progression. Consequently, researchers are vigorously exploring therapeutic strategies targeting BCR and its downstream pathways, including inhibitors of Bruton's tyrosine kinase (BTK) and PI3K, as well as direct BCR-targeted approaches. The central role of BCR signaling in lymphoma pathogenesis and treatment underscores its potential as a critical focus for future therapeutic development, offering new directions and hope for improved clinical outcomes.

Key words: B-cell lymphoma, B cell receptor, signal pathway, small molecule inhibitors, immunotherapy

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