| Literature DB >> 18794110 |
Millicent Winner1, Jason Meier, Swen Zierow, Beatriz E Rendon, Gregg V Crichlow, Randall Riggs, Richard Bucala, Lin Leng, Ned Smith, Elias Lolis, John O Trent, Robert A Mitchell.
Abstract
Although chemokine and growth factor receptors are attractive and popular targets for cancer therapeutic intervention, structure-based targeting of the ligands themselves is generally not considered practical. New evidence indicates that a notable exception to this is macrophage migration inhibitory factor (MIF). MIF, an autocrine- and paracrine-acting cytokine/growth factor, plays a pivotal role in both the initiation and maintenance of neoplastic diseases. MIF possesses a nonphysiologic enzymatic activity that is evolutionarily well-conserved. Although small molecule antagonists of MIFs enzymatic active site have been reported to inhibit biological activities of MIF, universally high IC(50)s have limited their clinical appeal. Using a computational virtual screening strategy, we have identified a unique small molecule inhibitor that serves as a suicide substrate for MIF, resulting in the covalent modification of the catalytically active NH(2)-terminal proline. Our studies further reveal that this compound, 4-iodo-6-phenylpyrimidine (4-IPP), is approximately 5x to 10x times more potent in blocking MIF-dependent catalysis and lung adenocarcinoma cell migration and anchorage-independent growth than the prototypical MIF inhibitor, ISO-1. Finally, using an in silico combinatorial optimization strategy, we have identified four unique congeners of 4-IPP that exhibit MIF inhibitory activity at concentrations 10x to 20x lower than that of parental 4-IPP.Entities:
Mesh:
Substances:
Year: 2008 PMID: 18794110 PMCID: PMC2726006 DOI: 10.1158/0008-5472.CAN-07-6227
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701