Macrophage Migration Inhibitory Factor (MIF) Enzymatic Activity and Lung Cancer

作者：Mawhinney Leona^*; Armstrong Michelle E; O' Reilly Ciaran; Bucala Richard; Leng Lin; Fingerle Rowson Gunter; Fayne Darren; Keane Michael P; Tynan Aisling; Maher Lewena; Cooke Gordon; Lloyd David; Conroy Helen; Donnelly Seamas C

来源：Molecular Medicine, 2014, 20(1): 729-735.

DOI：10.2119/molmed.2014.00136

The cytokine macrophage migration inhibitory factor (MIF) possesses unique tautomerase enzymatic activity, which contributes to the biological functional activity of MIF. In this study, we investigated the effects of blocking the hydrophobic active site of the tautomerase activity of MIF in the pathogenesis of lung cancer. To address this, we initially established a Lewis lung carcinoma (LLC) murine model in Mif-KO and wild-type (WT) mice and compared tumor growth in a knock-in mouse model expressing a mutant MIF lacking enzymatic activity (Mif(P1G)). Primary tumor growth was significantly attenuated in both Mif-KO and Mif(P1G) mice compared with WT mice. We subsequently undertook a structure-based, virtual screen to identify putative small molecular weight inhibitors specific for the tautomerase enzymatic active site of MIF. From primary and secondary screens, the inhibitor SCD-19 was identified, which significantly attenuated the tautomerase enzymatic activity of MIF in vitro and in biological functional screens. In the LLC murine model, SCD-19, given intraperitoneally at the time of tumor inoculation, was found to significantly reduce primary tumor volume by 90% (p %26lt; 0.001) compared with the control treatment. To better replicate the human disease scenario, SCD-19 was given when the tumor was palpable (at d 7 after tumor inoculation) and, again, treatment was found to significantly reduce tumor volume by 81% (p %26lt; 0.001) compared with the control treatment. In this report, we identify a novel inhibitor that blocks the hydrophobic pocket of MIF, which houses its specific tautomerase enzymatic activity, and demonstrate that targeting this unique active site significantly attenuates lung cancer growth in in vitro and in vivo systems.

• 出版日期2014-12