Mechanisms of drug inhibition of signalling molecules
- 24 May 2006
- journal article
- review article
- Published by Springer Nature in Nature
- Vol. 441 (7092), 457-462
- https://doi.org/10.1038/nature04874
Abstract
The emergence of tumour-specific, molecularly targeted agents signifies a paradigm shift in cancer therapy, with less reliance on drugs that non-discriminately kill tumour and host cells. Although the diversity of targets giving rise to this new generation of anticancer drugs has expanded, many challenges persist in the design of effective treatment regimens. The complex interplay of signal-transduction pathways further complicates the customization of cancer treatments to target single mechanisms. However, despite uncertainty over precise or dominant mechanisms of action, especially for compounds targeting multiple gene products, emerging agents are producing significant therapeutic advances against a broad range of human cancers.Keywords
This publication has 53 references indexed in Scilit:
- Signatures guide drug choiceNature, 2006
- BRAF mutation predicts sensitivity to MEK inhibitionNature, 2005
- Anti-erbB-2 antibody trastuzumab in the treatment of HER2-amplified breast cancerInvestigational New Drugs, 2005
- High Affinity Targets of Protein Kinase Inhibitors Have Similar Residues at the Positions Energetically Important for BindingJournal of Molecular Biology, 2005
- Targeted cancer therapyNature, 2004
- Structures of human MAP kinase kinase 1 (MEK1) and MEK2 describe novel noncompetitive kinase inhibitionNature Structural & Molecular Biology, 2004
- Mutations of the BRAF gene in human cancerNature, 2002
- Structural Mechanism for STI-571 Inhibition of Abelson Tyrosine KinaseScience, 2000
- The Hallmarks of CancerCell, 2000
- Activation Mechanism of the MAP Kinase ERK2 by Dual PhosphorylationCell, 1997