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小檗碱诱导的miRNA簇与mRNA之间信号通路的系统分析以及通过种子靶向抑制剂鉴定mir-99a∼125b簇在多发性骨髓瘤细胞中的功能

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.

作者信息

Feng Maoxiao, Luo Xiaochuang, Gu Chunming, Li Yumin, Zhu Xuejiao, Fei Jia

机构信息

a Department of Biochemistry and Molecular Biology; Medical College of Jinan University ; Guangzhou , China.

出版信息

RNA Biol. 2015;12(1):82-91. doi: 10.1080/15476286.2015.1017219.

Abstract

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.

摘要

背景

黄连素(BBR)是一种源自传统中草药的天然生物碱。然而,黄连素对骨髓瘤细胞产生不同作用的确切机制尚未完全阐明。

方法

采用系统分析方法整合黄连素处理后骨髓瘤细胞中由3个微小RNA(miRNA)簇和信使核糖核酸(mRNA)调控的常见信号通路。通过比较针对成熟miR - 125b的具有完全互补反义锁核酸(LNA)的t - 抗微小RNA(t - anti - mir)与抗miR - 125b的作用来确定miR - 99a ∼ 125b簇(骨髓瘤中一种重要的致癌微小RNA)的作用。

结果

在黄连素处理的骨髓瘤细胞中,3个miRNA簇(miR - 99a ∼ 125b、miR - 17 ∼ 92和miR - 106 ∼ 25)显著下调,并参与多种癌症相关信号通路。此外,前5个差异调节基因RAC1、NFκB1、MYC、JUN和CCND1可能在骨髓瘤进展中起关键作用。系统整合显示3条常见信号通路(TP53、Erb和MAPK)连接了3个miRNA簇和5个关键mRNA。同时,黄连素和靶向种子序列的t - 抗miR - 99a ∼ 125b簇LNA均显著诱导细胞凋亡、G2期细胞周期阻滞和集落抑制。

结论

我们的结果表明,黄连素部分通过下调3个miRNA簇和许多mRNA,可能通过TP53、Erb和MAPK信号通路来抑制多发性骨髓瘤细胞。miR - 99a ∼ 125b簇可能是骨髓瘤治疗的新靶点。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制见解。

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