The University of Texas MD Anderson Cancer Center, Department of Experimental Therapeutics, Houston, TX 77030, USA.
Expert Opin Investig Drugs. 2012 Apr;21(4):409-23. doi: 10.1517/13543784.2012.668526. Epub 2012 Mar 9.
Although protein kinases are primary targets for inhibition in hematological malignancies, until recently their contribution to chronic lymphocytic leukemia (CLL) was poorly understood. Insights into B-cell receptor signaling and its role in regulating key cellular functions have shed light on candidate protein kinases that are aberrantly activated in CLL. In this regard, protein kinases are now considered as potential drug targets in CLL.
This review has covered signaling pathways and associated protein kinases in CLL and the kinase inhibitors currently available in preclinical and clinical investigations. Individual protein kinases that are abnormally active in CLL and the functional consequences of their inhibition are discussed.
A growing body of evidence suggests that protein kinases are druggable targets for patients with CLL. The emergence of novel and bio-available kinase inhibitors and their promising clinical activity in CLL underscore the oncogenic role of kinases in leukemogenesis. Further investigations directed towards their role as single agents or in combinations may provide insight into understanding the substantial role of kinase-mediated signal transduction pathways and their inhibition in B- CLL.
尽管蛋白激酶是血液系统恶性肿瘤抑制的主要靶点,但直到最近,它们在慢性淋巴细胞白血病(CLL)中的作用仍知之甚少。对 B 细胞受体信号及其在调节关键细胞功能中的作用的深入了解揭示了在 CLL 中异常激活的候选蛋白激酶。在这方面,蛋白激酶现在被认为是 CLL 中的潜在药物靶点。
本综述涵盖了 CLL 中的信号通路和相关蛋白激酶,以及目前在临床前和临床研究中可用的激酶抑制剂。讨论了在 CLL 中异常活跃的个别蛋白激酶及其抑制的功能后果。
越来越多的证据表明,蛋白激酶是 CLL 患者可用药的靶点。新型生物可利用激酶抑制剂的出现及其在 CLL 中的有前景的临床活性强调了激酶在白血病发生中的致癌作用。进一步针对其作为单一药物或联合用药的作用的研究可能有助于了解激酶介导的信号转导途径及其在 B-CLL 中的抑制作用的重要作用。