Abstract

Background The histone methyltransferase SMYD3 (SET and MYND domain containing 3) is critical for vascular homeostasis and may be implicated in pathological angiogenesis. However, its mechanism remains elusive, and targeted inhibitors are in early-stage development. We aim to clarify whether SMYD3 regulates angiogenesis and develop novel molecules targeting SMYD3. Methods Expression profile of SMYD3 under pro-angiogenic conditions was characterized by bioinformatics analysis and endothelial cell (EC) validation. The effects of SMYD3 knockdown, knockdown-overexpression, and overexpression on angiogenesis were validated, including Matrigel neovascularization, aortic ring sprouting, and EC tube formation. Regarding molecule development, virtual screening, structural modifications, molecular docking, inhibition screening of EC proliferation, and SMYD3 enzyme activity and cellular thermal shift assays were employed. A novel molecule ZYZ329 was identified and evaluated in angiogenesis. Mechanistic studies involved genetic approaches and the mitochondrial reactive oxygen species (mROS) scavenger MitoQ (Mitoquinone mesylate). Finally, a murine hindlimb ischemia model and rat skin healing model were established to evaluate ZYZ329 on pathological and physiological angiogenesis. Results SMYD3 was upregulated in endothelial cells under ischemic, hypoxic, and VEGF-stimulated conditions. And SMYD3 gene knockdown, overexpression after knockdown, and overexpression regulated the angiogenesis capacity of endothelial cells. After virtual screening and structural modifications, the novel molecule ZYZ329 was developed for dual inhibition of EC proliferation (IC 50  = 6.147 μM) and SMYD3 enzymatic function (IC 50  = 0.419 μM). The ZYZ329 engaged SMYD3 in cells, and exhibited a certain degree of selectivity for SMYD3. Moreover, ZYZ329 significantly attenuated pathological angiogenesis in a dose-dependent manner. Mechanistically, genetic or pharmacological inhibition of SMYD3 impaired HI