UC San Diego Moores Cancer Center, La Jolla, CA 92093, USA.
Cancer J. 2012 Sep-Oct;18(5):404-10. doi: 10.1097/PPO.0b013e31826c5810.
The B-cell receptor (BCR) complex and its associated protein tyrosine kinases play a critical role in the development, proliferation, and survival of normal or malignant B cells. Regulated activity of the BCR complex promotes the expansion of selected B cells and the deletion of unwanted or self-reactive ones. Compounds that inhibit various components of this pathway, including spleen tyrosine kinase, Bruton's tyrosine kinase, and phosphoinositol-3 kinase, have been developed. We summarize the rationale for use of agents that can inhibit BCR signaling to treat patients with either indolent or aggressive B-cell lymphomas, highlight early clinical results, and speculate on the future application of such agents in the treatment of patients with various B-cell lymphomas.
B 细胞受体 (BCR) 复合物及其相关蛋白酪氨酸激酶在正常或恶性 B 细胞的发育、增殖和存活中发挥着关键作用。BCR 复合物的调节活性促进了选定的 B 细胞的扩增,并删除了不需要的或自身反应性的 B 细胞。已经开发了抑制该途径的各种成分的化合物,包括脾酪氨酸激酶、布鲁顿酪氨酸激酶和磷酸肌醇-3 激酶。我们总结了使用能够抑制 BCR 信号转导的药物来治疗惰性或侵袭性 B 细胞淋巴瘤患者的原理,强调了早期的临床结果,并推测了这些药物在治疗各种 B 细胞淋巴瘤患者中的未来应用。