Allen John C, Talab Fatima, Slupsky Joseph R
Department of Molecular & Clinical Pharmacology, Institute of Translational Medicine, University of Liverpool, Liverpool, L69 3GE, UK.
Redx Oncology Plc, Duncan Building, Royal Liverpool University Hospital, Daulby Street, Liverpool, L69 3GA, UK.
Int J Hematol Oncol. 2016 May;5(1):37-53. doi: 10.2217/ijh-2016-0003. Epub 2016 May 26.
B-lymphocytes are dependent on B-cell receptor (BCR) signaling for the constant maintenance of their physiological function, and in many B-cell malignancies this signaling pathway is prone to aberrant activation. This understanding has led to an ever-increasing interest in the signaling networks activated following ligation of the BCR in both normal and malignant cells, and has been critical in establishing an array of small molecule inhibitors targeting BCR-induced signaling. By dissecting how different malignancies signal through BCR, researchers are contributing to the design of more customized therapeutics which have greater efficacy and lower toxicity than previous therapies. This allows clinicians access to an array of approaches to best treat patients whose malignancies have BCR signaling as a driver of pathogenesis.
B淋巴细胞的生理功能持续维持依赖于B细胞受体(BCR)信号传导,在许多B细胞恶性肿瘤中,该信号通路易于发生异常激活。这种认识使得人们对正常和恶性细胞中BCR连接后激活的信号网络越来越感兴趣,并且对于建立一系列靶向BCR诱导信号传导的小分子抑制剂至关重要。通过剖析不同恶性肿瘤如何通过BCR进行信号传导,研究人员正在为设计更具针对性的疗法做出贡献,这些疗法比以前的疗法具有更高的疗效和更低的毒性。这使临床医生能够采用一系列方法,以最佳方式治疗其恶性肿瘤由BCR信号传导作为发病机制驱动因素的患者。