Drug Discovery Using Chemical Systems Biology: Weak Inhibition of Multiple Kinases May Contribute to the Anti-Cancer Effect of Nelfinavir

被引:134
作者
Xie, Li [1 ]
Evangelidis, Thomas [2 ]
Xie, Lei [1 ,3 ]
Bourne, Philip E. [1 ]
机构
[1] Univ Calif San Diego, Skaggs Sch Pharm & Pharmaceut Sci, La Jolla, CA 92093 USA
[2] Univ Manchester, Sch Pharm & Pharmaceut Sci, Manchester, Lancs, England
[3] CUNY Hunter Coll, Dept Comp Sci, New York, NY 10021 USA
关键词
HIV PROTEASE INHIBITORS; GENERALIZED BORN MODELS; MOLECULAR-DYNAMICS; FREE-ENERGIES; COMBINATION THERAPY; MULTITARGET DRUGS; IN-VITRO; BINDING; PROTEINS; SIMULATION;
D O I
10.1371/journal.pcbi.1002037
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
Nelfinavir is a potent HIV-protease inhibitor with pleiotropic effects in cancer cells. Experimental studies connect its anticancer effects to the suppression of the Akt signaling pathway, but the actual molecular targets remain unknown. Using a structural proteome-wide off-target pipeline, which integrates molecular dynamics simulation and MM/GBSA free energy calculations with ligand binding site comparison and biological network analysis, we identified putative human off-targets of Nelfinavir and analyzed the impact on the associated biological processes. Our results suggest that Nelfinavir is able to inhibit multiple members of the protein kinase-like superfamily, which are involved in the regulation of cellular processes vital for carcinogenesis and metastasis. The computational predictions are supported by kinase activity assays and are consistent with existing experimental and clinical evidence. This finding provides a molecular basis to explain the broad-spectrum anti-cancer effect of Nelfinavir and presents opportunities to optimize the drug as a targeted polypharmacology agent.
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页数:13
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