Cai Zhenguo, Zeng Yibin, Shi Xunlong, Zhang Xilin, Zhu Haiyan, Wang Wuqing
Department of Dermatology, Minhang Hospital, Fudan University, Central Hospital of Minhang District, Shanghai, China.
Department of Biological Medicines & Shanghai Engineering Research Center of Immunotherapeutics, Fudan University School of Pharmacy, Shanghai, China.
J Dermatol Sci. 2023 Feb;109(2):71-79. doi: 10.1016/j.jdermsci.2023.01.010. Epub 2023 Jan 29.
Benvitimod (Tapinarof), as a small-molecule topical therapeutical aryl hydrocarbon receptor (AHR)-modulating agent, is in clinical development for treating psoriasis and atopic dermatitis. Benvitimod reduces proinflammatory cytokines in psoriasis by specifically binding and activation of AHR. However, whether benvitimod can inhibit keratinocyte proliferation remains unclear. Minichromosome maintenance protein 6 (MCM6) is a key element of the prereplication complex (pre-RC) assembly which is one of the essential steps in the initiation of DNA replication for cell proliferation.
This study aimed to determine whether benvitimod could reduce the excessive proliferation of psoriatic keratinocytes by inhibiting MCM6.
We examined the inhibitory effect of benvitimod on MCM6-mediated proliferation of keratinocytes by HaCaT cells in vitro and an IMQ-induced psoriatic model of mice in vivo.
Epidermal MCM6 expression was enhanced in the skin lesions of psoriatic patients. The experiments further revealed that MCM6 was required for the proliferation of keratinocytes and governed by the IL-22/STAT3 pathway. In addition, the antiproliferation effect of benvitimod is achieved by the inhibition of p-JAK1 and p-JAK2, which further restrained the activation of STAT3 in keratinocytes. Lastly, benvitimod could repressed imiquimod-induced skin lesions and the expression of epidermal MCM6 and p-STAT3 in mice. Moreover, knockdown of AHR in keratinocytes enhanced the activation of JAK1 and JAK2.
The findings reveal that benvitimod could decrease MCM6-mediated proliferation of keratinocytes by affecting the JAK/STAT3 pathway, thereby serving as a new treatment modality for psoriasis.
本维莫德(Tapinarof)作为一种小分子局部治疗性芳烃受体(AHR)调节剂,正在进行治疗银屑病和特应性皮炎的临床开发。本维莫德通过特异性结合和激活AHR来降低银屑病中的促炎细胞因子。然而,本维莫德是否能抑制角质形成细胞增殖仍不清楚。微小染色体维持蛋白6(MCM6)是复制前复合体(pre-RC)组装的关键元件,而pre-RC组装是细胞增殖过程中DNA复制起始的必要步骤之一。
本研究旨在确定本维莫德是否能通过抑制MCM6来减少银屑病角质形成细胞的过度增殖。
我们在体外通过HaCaT细胞以及在体内通过咪喹莫特诱导的小鼠银屑病模型,研究了本维莫德对MCM6介导的角质形成细胞增殖的抑制作用。
银屑病患者皮肤病变中表皮MCM6表达增强。实验进一步表明,MCM6是角质形成细胞增殖所必需的,且受IL-22/STAT3途径调控。此外,本维莫德的抗增殖作用是通过抑制p-JAK1和p-JAK2实现的,这进一步抑制了角质形成细胞中STAT3的激活。最后,本维莫德可抑制咪喹莫特诱导的小鼠皮肤病变以及表皮MCM6和p-STAT3的表达。此外,角质形成细胞中AHR的敲低增强了JAK1和JAK2的激活。
研究结果表明,本维莫德可通过影响JAK/STAT3途径来减少MCM6介导的角质形成细胞增殖,从而成为银屑病的一种新治疗方式。