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Triterpenoid corosolic acid modulates global CpG methylation and transcriptome of tumor promotor TPA induced mouse epidermal JB6 P+ cells.

三萜科罗索酸调节肿瘤启动子TPA诱导的小鼠表皮JB6 P + 细胞的整体CpG甲基化和转录组。

  • 影响因子:3.43
  • DOI:10.1016/j.cbi.2020.109025
  • 作者列表:"Hudlikar RR","Sargsyan D","Wu R","Su S","Zheng M","Kong AN
  • 发表时间:2020-04-25
Abstract

:Epigenetic regulation is one of the driving forces in the process of carcinogenesis. Corosolic acid (CA); triterpenoid abundantly found in Lagerstroemia speciosa L. is known to modulate various cellular process including cellular oxidative stress and signaling kinases in various diseases, including skin cancer. Genetic mutations in early stages of skin cancer are well-documented, the epigenetic alterations remain elusive. In the present study, we identified the transcriptomic gene expression changes with RNAseq and genome-wide DNA CpG methylation changes with DNA methylseq to profile the early stage transcriptomic and epigenomic changes using tumor promoter TPA-mediated mouse epidermal epithelial JB6 P+ cells. JB6 P+ cells were treated with TPA and Corosolic acid by 7.5uM optimized by MTS assay. Differentiated expressed genes (DEGs) and Differentially methylated genes (DMRs) were analyzed by R software. Ingenuity Pathway Analysis (IPA) was employed to understand the differential regulation of specific pathways. Novel TPA induced differentially overexpressed genes like tumor promoter Prl2c2, small prolin rich protein (Sprr2h) was reported which was downregulated by corosolic acid treatment. Several cancer related pathways were identified by Ingenuity Pathways Analysis (IPA) including p53, Erk, TGF beta signaling pathways. Moreover, differentially methylated regions (DMRs) in genes like Dusp22 (Dual specificity protein phosphatase 22), Rassf (tumor suppressor gene family, Ras association domain family) in JB6 P+ cells were uncovered which are altered by TPA and are reversed by CA treatment. Interestingly, genes like CDK1 (Cyclin-dependent kinases 1) and RASSF2 (Ras association domain family member 2) observed to be differentially methylated and expressed which was further modulated by corosolic acid treatment, validated by qPCR. Given study indicated gene expression changes to DNA CpG methylation epigenomic changes modulated various molecular pathways in TPA-induced JB6 cells and revealed that CA can potentially reverse these changes which deciphering novel molecular targets for future prevention of early stages of skin cancer studies in human.

摘要

: 表观遗传调控是致癌过程的驱动力之一。科罗索酸 (CA); 三萜类化合物大量存在于大叶紫薇中。已知可调节各种细胞过程,包括细胞氧化应激和各种疾病中的信号激酶,包括皮肤癌。皮肤癌早期阶段的基因突变有很好的记录,表观遗传改变仍然难以捉摸。在本研究中,我们用RNAseq鉴定了转录组基因表达变化,用DNA methylseq鉴定了全基因组DNA CpG甲基化变化,用肿瘤启动子TPA介导的小鼠表皮JB6 P描述了早期转录组和表观基因组变化。+ 细胞。通过MTS试验优化的 7.5uM用TPA和科罗索酸处理JB6 P + 细胞。用R软件分析差异表达基因 (DEGs) 和差异甲基化基因 (DMRs)。采用独创性通路分析 (IPA) 了解特定通路的差异调控。报道了新的TPA诱导的肿瘤启动子Prl2c2 等差异过表达基因,小的富含脯氨酸蛋白 (Sprr2h) 被科罗索酸处理下调。通过独创性通路分析 (IPA) 确定了几种癌症相关通路,包括p53 、Erk、TGF β 信号通路。此外,差异甲基化区域 (DMRs) 基因如Dusp22 (双特异性蛋白磷酸酶 22),Rassf (肿瘤抑制基因家族,Ras关联域家族) 在JB6 中发现P + 细胞被TPA改变,并被CA处理逆转。有趣的是,像CDK1 (细胞周期蛋白依赖性激酶 1) 和RASSF2 (Ras关联域家族成员 2) 这样的基因观察到差异甲基化和表达,这被科罗索酸处理进一步调节。通过qPCR验证。给定的研究表明DNA CpG甲基化的基因表达变化表观基因组变化调节TPA诱导的JB6 细胞中的各种分子通路,并揭示CA可以潜在地逆转这些变化,从而破译新的分子靶点用于未来的预防。人类皮肤癌研究的早期阶段。

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影响因子:2.93
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影响因子:0.96
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皮肤肿瘤方向

皮肤肿瘤是发生在皮肤的细胞增生性疾病,是一种常见病。发生于皮内或皮下组织的新生物,种类很多,临床上分良性肿瘤和恶性肿瘤。恶性肿瘤可以不断增殖,引起转移,威胁生命,称为皮肤癌。

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