Unleashing the power of inhibitors of oncogenic kinases through BH3 mimetics

被引:146
作者
Cragg, Mark S. [1 ,3 ]
Harris, Claire [3 ]
Strasser, Andreas [1 ]
Scott, Clare L. [1 ,2 ]
机构
[1] Walter & Eliza Hall Inst Med Res, Melbourne, Vic 3050, Australia
[2] Royal Melbourne Hosp, Dept Med Oncol, Melbourne, Vic 3050, Australia
[3] Univ Southampton, Canc Sci Div, Sch Med, Southampton Gen Hosp, Southampton SO16 6YD, Hants, England
关键词
BCL-2 FAMILY PROTEINS; SMALL-MOLECULE INHIBITOR; B-CELL LYMPHOMA; LUNG-CANCER; EGFR MUTATIONS; ABL KINASE; IN-VITRO; ABT-737; RESISTANCE; APOPTOSIS;
D O I
10.1038/nrc2615
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Therapeutic targeting Of tumours on the basis of molecular analysis is a new paradigm for cancer treatment but has yet to fulfil expectations. For many solid tumours, targeted therapeutics, such as inhibitors of oncogenic kinase pathways, elicit predominantly disease-stabilizing, Cytostatic responses, rather than tumour regression. Combining oncogenic kinase inhibitors with direct activators of the apoptosis machinery, Such as the BH3 mimetic ABT-737, may unlock potent anti-tumour potential to produce durable clinical responses with less collateral damage.
引用
收藏
页码:321 / 326
页数:6
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