Hydroxamate-Based Selective Macrophage Elastase (MMP-12) Inhibitors and Radiotracers for Molecular Imaging
journal contributionposted on 18.11.2020, 20:06 by Kiran Gona, Jakub Toczek, Yunpeng Ye, Nowshin Sanzida, Arvene Golbazi, Parnaz Boodagh, Mani Salarian, Jae-Joon Jung, Saranya Rajendran, Gunjan Kukreja, Terence L. Wu, Laurent Devel, Mehran M. Sadeghi
Macrophage elastase [matrix metalloproteinase (MMP)-12] is the most upregulated MMP in abdominal aortic aneurysm (AAA) and, hence, MMP-12-targeted imaging may predict AAA progression and rupture risk. Here, we report the design, synthesis, and evaluation of three novel hydroxamate-based selective MMP-12 inhibitors (CGA, CGA-1, and AGA) and the methodology to obtain MMP-12 selectivity from hydroxamate-based panMMP inhibitors. Also, we report two 99mTc-radiotracers, 99mTc-AGA-1 and 99mTc-AGA-2, derived from AGA. 99mTc-AGA-2 displayed faster blood clearance in mice and better radiochemical stability compared to 99mTc-AGA-1. Based on this, 99mTc-AGA-2 was chosen as the lead tracer and tested in murine AAA. 99mTc-AGA-2 uptake detected by autoradiography was significantly higher in AAA compared to normal aortic regions. Specific binding of the tracer to MMP-12 was demonstrated through ex vivo competition. Accordingly, this study introduces a novel family of selective MMP-12 inhibitors and tracers, paving the way for further development of these agents as therapeutic and imaging agents.
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aortic aneurysmMMP -12 selectivityaortic regionsMolecular Imaging Macrophage elastase99 m Tc-AGA -2 uptakeradiochemical stability99 m Tc-AGA -2rupture riskMMP -12hydroxamate-based panMMP inhibitorsupregulated MMP99 m Tc-AGAmurine AAAMMP -12 inhibitorsCGAmatrix metalloproteinase99 m Tc-AGA -1.novel hydroxamate-basedSpecific bindingMMP -12-targeted imagingMacrophage Elastasenovel familyAAA progressionvivo competition99 m Tc-radiotracersimaging agentsblood clearance