Hypoxia inducible factor (HIF) as a model for studying inhibition of protein-protein interactions

被引:34
作者
Burslem, George M. [1 ,2 ]
Kyle, Hannah F. [2 ,3 ]
Nelson, Adam [1 ,2 ]
Edwards, Thomas A. [2 ,3 ]
Wilson, Andrew J. [1 ,2 ]
机构
[1] Univ Leeds, Sch Chem, Woodhouse Lane, Leeds LS2 9JT, W Yorkshire, England
[2] Univ Leeds, Astbury Ctr Struct Mol Biol, Woodhouse Lane, Leeds LS2 9JT, W Yorkshire, England
[3] Univ Leeds, Fac Biol Sci, Sch Mol & Cellular Biol, Woodhouse Lane, Leeds LS2 9JT, W Yorkshire, England
基金
欧洲研究理事会; 英国生物技术与生命科学研究理事会; 英国工程与自然科学研究理事会;
关键词
SMALL-MOLECULE INHIBITORS; RENAL-CELL CARCINOMA; E3 UBIQUITIN LIGASE; PAS-B DOMAIN; STRUCTURAL BASIS; SIGNAL-TRANSDUCTION; TUMOR-GROWTH; FACTOR-I; TRANSCRIPTIONAL RESPONSE; PEPTIDE LIBRARIES;
D O I
10.1039/c7sc00388a
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
The modulation of protein-protein interactions (PPIs) represents a major challenge in modern chemical biology. Current approaches (e.g. high-throughput screening, computer aided ligand design) are recognised as having limitations in terms of identification of hit matter. Considerable success has been achieved in terms of developing new approaches to PPI modulator discovery using the p53/hDM2 and Bcl-2 family of PPIs. However these important targets in oncology might be considered as "low-hanging-fruit". Hypoxia inducible factor (HIF) is an emerging, but not yet fully validated target for cancer chemotherapy. Its role is to regulate the hypoxic response and it does so through a plethora of protein-protein interactions of varying topology, topography and complexity: its modulation represents an attractive approach to prevent development of new vasculature by hypoxic tumours.
引用
收藏
页码:4188 / 4202
页数:15
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