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Systematic analysis of berberine-induced signaling pathway between miRNA clusters and mRNAs and identification of mir-99a similar to 125b cluster function by seed-targeting inhibitors in multiple myeloma cells

机译:小ber碱诱导的miRNA簇与mRNA之间的信号转导途径的系统分析和种子靶向抑制剂在多发性骨髓瘤细胞中鉴定类似于125b簇功能的mir-99a

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Background: Berberine (BBR) is a natural alkaloid derived from a traditional Chinese herbal medicine. However, the exact mechanisms underlying the different effects of berberine on MM cells have not been fully elucidated. Methods: A systematic analysis assay integrated common signaling pathways modulated by the 3 miRNA clusters and mRNAs in MM cells after BBR treatment. The role of the mir-99a similar to 125b cluster, an important oncomir in MM, was identified by comparing the effects of t-anti-mirs with complete complementary antisense locked nucleic acids (LNAs) against mature mir-125b (anti-mir-125b). Results: Three miRNAs clusters (miR-99a similar to 125b, miR-17 similar to 92 and miR-106 similar to 25) were significantly down-regulated in BBR-treated MM cells and are involved in multiple cancer-related signaling pathways. Furthermore, the top 5 differentially regulated genes, RAC1, NF kappa B1, MYC, JUN and CCND1 might play key roles in the progression of MM. Systematic integration revealed that 3 common signaling pathways (TP53, Erb and MAPK) link the 3 miRNA clusters and the 5 key mRNAs. Meanwhile, both BBR and seed-targeting t-anti-mir-99a similar to 125b cluster LNAs significantly induced apoptosis, G2-phase cell cycle arrest and colony inhibition. Conclusions: our results suggest that BBR suppresses multiple myeloma cells, partly by down-regulating the 3 miRNA clusters and many mRNAs, possibly through TP53, Erb and MAPK signaling pathways. The mir-99a similar to 125b cluster might be a novel target for MM treatment. These findings provide new mechanistic insight into the anticancer effects of certain traditional Chinese herbal medicine compounds.
机译:背景:小ber碱(BBR)是源自传统中草药的天然生物碱。然而,黄连素对MM细胞不同作用的确切机制尚未完全阐明。方法:系统分析分析整合了BBR治疗后MM细胞中3个miRNA簇和mRNA调控的常见信号通路。通过比较带有完整互补反义锁核酸(LNA)的t-反-mirs对成熟mir-125b(anti-mir- 125b)。结果:三个miRNA簇(类似于125b的miR-99a,类似于92的miR-17和类似于25的miR-106)在BBR处理的MM细胞中显着下调,并参与多种与癌症相关的信号通路。此外,前5个差异调节基因RAC1,NF kappa B1,MYC,JUN和CCND1可能在MM的发展中起关键作用。系统整合显示,3个常见的信号通路(TP53,Erb和MAPK)将3个miRNA簇和5个关键mRNA关联起来。同时,类似于125b簇LNA的BBR和靶向种子的t-anti-mir-99a均显着诱导凋亡,G2期细胞周期阻滞和集落抑制。结论:我们的结果表明BBR可能通过TP53,Erb和MAPK信号通路部分抑制了3个miRNA簇和许多mRNA,从而抑制了多发性骨髓瘤细胞。类似于125b簇的mir-99a可能是MM治疗的新靶标。这些发现为某些传统中草药化合物的抗癌作用提供了新的机理见解。

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