Combining imaging and pathway profiling: an alternative approach to cancer drug discovery

被引:18
作者
Carragher, Neil O. [1 ]
Brunton, Valerie G. [1 ]
Frame, Margaret C. [1 ]
机构
[1] Univ Edinburgh, Edinburgh Canc Res UK Ctr, Inst Genet & Mol Med, Edinburgh EH4 2XR, Midlothian, Scotland
关键词
PHASE PROTEIN ARRAY; SOFTWARE ENVIRONMENT; SYSTEMS BIOLOGY; GENE-EXPRESSION; SMALL MOLECULES; CELL-MOVEMENT; BREAST-CANCER; TARGETING SRC; E-CADHERIN; IN-VIVO;
D O I
10.1016/j.drudis.2012.02.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Conventional drug discovery strategies are typically 'target centric' based on the selection of lead compounds with optimised 'on-target' potency and selectivity profiles. However, high-attrition rates are often the result of compensatory or redundant cancer mechanisms and the fact that tumours do not find it difficult to escape inhibition of a single pathway. In this article, we highlight two emerging and complimentary technologies; namely phenotypic imaging and post-translational pathway profiling, which when combined with relevant disease models can provide pharmacodiagnostic and drug combination strategies that predict and counteract inherent and adaptive drug resistance. The implementation of such approaches at early stages of the drug discovery process enables more informed decisions on candidate drug selection and how to maximise and predict efficacy before clinical development.
引用
收藏
页码:203 / 214
页数:12
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