Department of Biomedical and Pharmaceutical Sciences, University of Montana, Missoula, Montana, USA.
URPHYM-NARILIS, University of Namur, Namur, Belgium.
J Invest Dermatol. 2021 Jan;141(1):72-83.e6. doi: 10.1016/j.jid.2020.05.090. Epub 2020 Jun 4.
Inhibition of CYP450-mediated retinoic acid (RA) metabolism by RA metabolism blocking agents increases endogenous retinoids and is an alternative to retinoid therapy. Currently available RA metabolism blocking agents (i.e., liarozole and talarozole) tend to have fewer adverse effects than traditional retinoids but lack target specificity. Substrate-based inhibitor DX314 has enhanced selectivity for RA-metabolizing enzyme CYP26B1 and may offer an improved treatment option for keratinization disorders such as congenital ichthyosis and Darier disease. In this study, we used RT-qPCR, RNA sequencing, pathway, upstream regulator, and histological analyses to demonstrate that DX314 can potentiate the effects of all-trans-RA in healthy and diseased reconstructed human epidermis. We unexpectedly discovered that DX314, but not all-trans-RA or previous RA metabolism blocking agents, appears to protect epidermal barrier integrity. In addition, DX314-induced keratinization and epidermal proliferation effects are observed in a rhino mice model. Altogether, the results indicate that DX314 inhibits all-trans-RA metabolism with minimal off-target activity and shows therapeutic similarity to topical retinoids in vitro and in vivo. Findings of a barrier-protecting effect require further mechanistic study but may lead to a unique strategy in barrier-reinforcing therapies. DX314 is a promising candidate compound for further study and development in the context of keratinization disorders.
RA 代谢阻断剂抑制 CYP450 介导的视黄酸(RA)代谢,增加内源性视黄酸,是视黄酸治疗的替代方法。目前可用的 RA 代谢阻断剂(即利亚唑和他拉唑)往往比传统视黄酸的不良反应更少,但缺乏靶向特异性。基于底物的抑制剂 DX314对 RA 代谢酶 CYP26B1 具有更高的选择性,可能为角化障碍(如先天性鱼鳞病和大疱性表皮松解症)提供一种改进的治疗选择。在这项研究中,我们使用 RT-qPCR、RNA 测序、途径、上游调节剂和组织学分析来证明 DX314 可以增强全反式 RA 在健康和患病重建人体表皮中的作用。我们出人意料地发现,DX314(而非全反式 RA 或以前的 RA 代谢阻断剂)似乎可以保护表皮屏障的完整性。此外,在 rhino 小鼠模型中观察到 DX314 诱导的角化和表皮增殖作用。总之,结果表明 DX314 抑制全反式 RA 代谢,具有最小的脱靶活性,并在体外和体内显示出与局部视黄酸相似的治疗效果。关于屏障保护作用的发现需要进一步的机制研究,但可能会导致在屏障强化治疗方面的独特策略。DX314 是一种有前途的候选化合物,可在角化障碍的背景下进一步研究和开发。