TY - JOUR
T1 - Combining imaging and pathway profiling: an alternative approach to cancer drug discovery.
AU - Carragher, Neil
AU - Brunton, Val
AU - Frame, Margaret
PY - 2012/3
Y1 - 2012/3
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=84857992908&partnerID=8YFLogxK
U2 - 10.1016/j.drudis.2012.02.002
DO - 10.1016/j.drudis.2012.02.002
M3 - Article
SN - 1359-6446
VL - 17
SP - 203
EP - 214
JO - Drug Discovery Today
JF - Drug Discovery Today
IS - 5-6
ER -