首页> 美国卫生研究院文献>RNA Biology >Systematic analysis of berberine-induced signaling pathway between miRNA clusters and mRNAs and identification of mir-99a∼125b cluster function by seed-targeting inhibitors in multiple myeloma cells
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Systematic analysis of berberine-induced signaling pathway between miRNA clusters and mRNAs and identification of mir-99a∼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mir-99a〜125b簇的功能

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摘要

>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∼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∼125b, miR-17∼92 and miR-106∼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, NFκB1, 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∼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∼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。但是,尚未完全阐明黄连素对MM细胞的不同作用的确切机制。 >方法:一种系统分析方法,整合了BBR处理后MM细胞中3个miRNA簇和mRNA调控的常见信号通路。通过比较具有完整互补反义锁核酸(LNA)的t-anti-mirs对成熟mir-125b(anti-mir-125b)的作用,确定了mir-99a〜125b簇(MM中重要的发病分子)的作用。 )。 >结果:在BBR处理的MM细胞中,三个miRNA簇(miR-99a〜125b,miR-17〜92和miR-106〜25)显着下调,并参与了多种与癌症相关的活动信号通路。此外,前5个差异调节基因RAC1,NFκB1,MYC,JUN和CCND1可能在MM的发展中起关键作用。系统性整合显示,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,BBR和靶向种子的t-anti-mir-99a〜125b簇LNAs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的表达,从而抑制了多发性骨髓瘤细胞。 mir-99a〜125b簇可能是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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