Centre for Craniofacial and Regenerative Biology, Guy's Hospital, King's College London, London SE1 9RT, UK.
Int J Mol Sci. 2020 Sep 2;21(17):6394. doi: 10.3390/ijms21176394.
One of the main goals of dentistry is the natural preservation of the tooth structure following damage. This is particularly implicated in deep dental cavities affecting dentin and pulp, where odontoblast survival is jeopardized. This activates pulp stem cells and differentiation of new odontoblast-like cells, accompanied by increased Wnt signaling. Our group has shown that delivery of small molecule inhibitors of GSK3 stimulates Wnt/β-catenin signaling in the tooth cavity with pulp exposure and results in effective promotion of dentin repair. Small molecules are a good therapeutic option due to their ability to pass across cell membranes and reach target. Here, we investigate a range of non-GSK3 target small molecules that are currently used for treatment of various medical conditions based on other kinase inhibitory properties. We analyzed the ability of these drugs to stimulate Wnt signaling activity by off-target inhibition of GSK3. Our results show that a c-Met inhibitor, has the ability to stimulate Wnt/β-catenin pathway in dental pulp cells in vitro at low concentrations. This work is an example of drug repurposing for dentistry and suggests a candidate drug to be tested in vivo for natural dentin repair. This approach bypasses the high level of economical and time investment that are usually required in novel drug discoveries.
牙科的主要目标之一是在损伤后自然保存牙齿结构。这在深达牙本质和牙髓的龋齿中尤为重要,因为牙本质细胞的存活受到威胁。这会激活牙髓干细胞并分化为新的成牙本质细胞样细胞,同时伴随着 Wnt 信号的增加。我们的研究小组已经表明,在暴露牙髓的牙腔内递送 GSK3 小分子抑制剂可刺激 Wnt/β-连环蛋白信号通路,从而有效促进牙本质修复。小分子是一种很好的治疗选择,因为它们能够穿过细胞膜并到达靶点。在这里,我们研究了一系列目前基于其他激酶抑制特性用于治疗各种医学病症的非 GSK3 靶小分子。我们分析了这些药物通过非靶标抑制 GSK3 刺激 Wnt 信号活性的能力。我们的结果表明,低浓度的 c-Met 抑制剂能够在体外刺激牙髓细胞中的 Wnt/β-连环蛋白通路。这项工作是牙科药物再利用的一个例子,并为天然牙本质修复提供了一种候选药物,有待在体内进行测试。这种方法绕过了新药发现通常需要的大量经济和时间投入。