Xu Yang, Zhou Bingrong, Wu Di, Yin Zhiqiang, Luo Dan
Department of Dermatology, the First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu 210029, China.
J Biomed Res. 2012 Mar;26(2):125-34. doi: 10.1016/S1674-8301(12)60022-0.
This study aimed to evaluate the effects of baicalin on ultraviolet radiation B (UVB)-mediated microRNA (miRNA) expression in mouse skin. We determined miRNA expression profiles in UVB irradiated mice, baicalin treated irradiated mice, and untreated mice, and conducted TargetScan and Gene Ontology analyses to predict miRNA targets. Three miRNAs (mmu-miR-125a-5p, mmu-miR-146a, and mmu-miR-141) were downregulated and another three (mmu-miR-188-5p, mmu-miR-223 and mmu-miR-22) were upregulated in UVB irradiated mice compared with untreated mice. Additionally, these miRNAs were predicted to be related to photocarcinogenesis, hypomethylation and apoptosis. Three miRNAs (mmu-miR-378, mmu-miR-199a-3p and mmu-miR-181b) were downregulated and one (mmu-miR-23a) was upregulated in baicalin treated mice compared with UVB irradiated mice, and they were predicted to be related to DNA repair signaling pathway. These deregulated miRNAs are potentially involved in the pathogenesis of photodamage, and may aid treatment and prevention of UVB-induced dermatoses.
本研究旨在评估黄芩苷对紫外线B(UVB)介导的小鼠皮肤微小RNA(miRNA)表达的影响。我们测定了UVB照射小鼠、黄芩苷处理的照射小鼠和未处理小鼠的miRNA表达谱,并进行了TargetScan和基因本体分析以预测miRNA靶标。与未处理小鼠相比,UVB照射小鼠中有三种miRNA(mmu-miR-125a-5p、mmu-miR-146a和mmu-miR-141)表达下调,另外三种(mmu-miR-188-5p、mmu-miR-223和mmu-miR-22)表达上调。此外,预测这些miRNA与光致癌作用、低甲基化和细胞凋亡有关。与UVB照射小鼠相比,黄芩苷处理的小鼠中有三种miRNA(mmu-miR-378、mmu-miR-199a-3p和mmu-miR-181b)表达下调,一种(mmu-miR-23a)表达上调,并且预测它们与DNA修复信号通路有关。这些失调的miRNA可能参与了光损伤的发病机制,并且可能有助于UVB诱导的皮肤病的治疗和预防。