Targeting Brutons Tyrosine Kinase in Chronic Lymphocytic Leukemia at the Crossroad between Intrinsic and Extrinsic Pro-survival Signals

F. Frezzato, V. Trimarco, A. Visentin, V. Martini, Filippo Severin, M. Facco, G. Semenzato, L. Trentin
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引用次数: 5

Abstract

Chemo immunotherapies for chronic lymphocytic leukemia (CLL) showed a positive impact on clinical outcome, but many patients relapsed or become refractory to the available treatments. The main goal of the researchers in CLL is the identification of specific targets in order to develop new therapeutic strategies to cure the disease. The Bcell receptor-signalling pathway is necessary for survival of malignant B cells and its related molecules recently become new targets for therapy. Moreover, leukemic microenvironment delivers survival signals to neoplastic cells also overcoming the apoptotic effect induced by traditional drugs. In this context, the investigation of Bruton’s tyrosine kinase (Btk) is useful in: i) dissecting CLL pathogenesis; ii) finding new therapeutic approaches striking simultaneously intrinsic as well as extrinsic pro-survival signals in CLL. This paper will review these main topics.
靶向布鲁顿酪氨酸激酶在慢性淋巴细胞白血病中的内在和外在促生存信号的交叉点
慢性淋巴细胞白血病(CLL)的化疗免疫治疗对临床结果有积极影响,但许多患者复发或对现有治疗变得难治。CLL研究人员的主要目标是确定特定的靶点,以便开发新的治疗策略来治愈这种疾病。B细胞受体信号通路是恶性B细胞生存所必需的,其相关分子近年来成为治疗的新靶点。此外,白血病微环境向肿瘤细胞传递生存信号,也克服了传统药物诱导的凋亡效应。在这种情况下,布鲁顿酪氨酸激酶(Btk)的研究有助于:1)解剖CLL发病机制;ii)寻找新的治疗方法,同时打击CLL的内在和外在促生存信号。本文将回顾这些主要主题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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