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全基因组DNA甲基化增强肿瘤再增殖细胞机械分选过程中的干性

Genome-Wide DNA Methylation Enhances Stemness in the Mechanical Selection of Tumor-Repopulating Cells.

作者信息

Huang Wei, Hu Hui, Zhang Qiong, Wang Ning, Yang Xiangliang, Guo An-Yuan

机构信息

National Engineering Research Center for Nanomedicine, College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan, China.

Center for Artificial Intelligence Biology, Hubei Bioinformatics & Molecular Imaging Key Laboratory, Key Laboratory of Molecular Biophysics of the Ministry of Education, College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan, China.

出版信息

Front Bioeng Biotechnol. 2020 Mar 17;8:88. doi: 10.3389/fbioe.2020.00088. eCollection 2020.

Abstract

BACKGROUND

DNA methylation plays essential roles in tumor occurrence and stemness maintenance. Tumor-repopulating cells (TRCs) are cancer stem cell (CSC)-like cells with highly tumorigenic and self-renewing abilities, which were selected from tumor cells in soft three-dimensional (3D) fibrin gels.

METHODS

Here, we presented a genome-wide map of methylated cytosines for time-series samples in TRC selection, in a 3D culture using whole-genome bisulfite sequencing (WGBS).

RESULTS

A comparative analysis revealed that the methylation degrees of many differentially methylated genes (DMGs) were increased by the mechanical environment and changed from 2D rigid to 3D soft. DMGs were significantly enriched in stemness-related terms. In 1-day, TRCs had the highest non-CG methylation rate indicating its strong stemness. We found that genes with continuously increasing or decreasing methylation like may also affect the TRC screening process. Furthermore, results showed that stage-specific/common CSCs markers were biased toward changing their methylation in non-CG (CHG and CHH, where H corresponds to A, T, or C) methylation and enriched in gene body region.

CONCLUSIONS

WGBS provides DNA methylome in TRC screening. It was confirmed that non-CG DNA methylation plays an important role in TRC selection, which indicates that it is more sensitive to mechanical microenvironments and affects TRCs by regulating the expression of stemness genes in tumor cells.

摘要

背景

DNA甲基化在肿瘤发生和干性维持中起着至关重要的作用。肿瘤再增殖细胞(TRCs)是具有高度致瘤性和自我更新能力的癌症干细胞(CSC)样细胞,是从软三维(3D)纤维蛋白凝胶中的肿瘤细胞中筛选出来的。

方法

在此,我们使用全基因组亚硫酸氢盐测序(WGBS),展示了在3D培养的TRC选择过程中,时间序列样本中甲基化胞嘧啶的全基因组图谱。

结果

一项比较分析显示,许多差异甲基化基因(DMGs)的甲基化程度因机械环境而增加,并从二维刚性环境转变为三维软环境。DMGs在干性相关术语中显著富集。在第1天,TRCs具有最高的非CG甲基化率,表明其干性很强。我们发现,甲基化持续增加或减少的基因可能也会影响TRC筛选过程。此外,结果表明,阶段特异性/常见的CSCs标志物倾向于在非CG(CHG和CHH,其中H对应于A、T或C)甲基化中改变其甲基化,并在基因体区域富集。

结论

WGBS提供了TRC筛选中的DNA甲基化组。证实了非CG DNA甲基化在TRC选择中起重要作用,这表明它对机械微环境更敏感,并通过调节肿瘤细胞中干性基因的表达来影响TRCs。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8043/7090028/9321cb78e3f8/fbioe-08-00088-g001.jpg

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