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肺腺癌吸烟者中受表观遗传调控的长链非编码 RNA 和 DNA 甲基化的全景图。

Landscape of epigenetically regulated lncRNAs and DNA methylation in smokers with lung adenocarcinoma.

机构信息

Department of Pathology, International St. Mary's Hospital, Catholic Kwandong University College of Medicine, Incheon, Republic of Korea.

Department of Pathology, Anam Hospital, Korea University College of Medicine, Seoul, Republic of Korea.

出版信息

PLoS One. 2021 Mar 8;16(3):e0247928. doi: 10.1371/journal.pone.0247928. eCollection 2021.

Abstract

In this study, we identified long non-coding RNAs (lncRNAs) associated with DNA methylation in lung adenocarcinoma (LUAD) using clinical and methylation/expression data from 184 qualified LUAD tissue samples and 21 normal lung-tissue samples from The Cancer Genome Atlas (TCGA). We identified 1865 differentially expressed genes that correlated negatively with the methylation profiles of normal lung tissues, never-smoker LUAD tissues and smoker LUAD tissues, while 1079 differentially expressed lncRNAs were identified using the same criteria. These transcripts were integrated using ingenuity pathway analysis to determine significant pathways directly related to cancer, suggesting that lncRNAs play a crucial role in carcinogenesis. When comparing normal lung tissues and smoker LUAD tissues, 86 candidate genes were identified, including six lncRNAs. Of the 43 candidate genes revealed by comparing never-smoker LUAD tissues and smoker LUAD tissues, 13 were also different when compared to normal lung tissues. We then investigated the expression of these genes using the Gene Expression of Normal and Tumor Tissues (GENT) and Methylation and Expression Database of Normal and Tumor Tissues (MENT) databases. We observed an inverse correlation between the expression of 13 genes in normal lung tissues and smoker LUAD tissues, and the expression of five genes between the never-smoker and smoker LUAD tissues. These findings were further validated in clinical specimens using bisulfite sequencing, revealing that AGR2, AURKB, FOXP3, and HMGA1 displayed borderline differences in methylation. Finally, we explored the functional connections between DNA methylation, lncRNAs, and gene expression to identify possible targets that may contribute toward the pathogenesis of cigarette smoking-associated LUAD. Together, our findings suggested that differentially expressed lncRNAs and their target transcripts could serve as potential biomarkers for LUAD.

摘要

在这项研究中,我们使用来自 184 个合格的肺腺癌 (LUAD) 组织样本和 21 个来自癌症基因组图谱 (TCGA) 的正常肺组织样本的临床和甲基化/表达数据,鉴定了与 LUAD 中 DNA 甲基化相关的长非编码 RNA (lncRNA)。我们鉴定了 1865 个差异表达基因,这些基因与正常肺组织、从不吸烟者 LUAD 组织和吸烟者 LUAD 组织的甲基化图谱呈负相关,而使用相同标准鉴定了 1079 个差异表达的 lncRNA。这些转录物通过使用 Ingenuity 通路分析进行整合,以确定与癌症直接相关的显著通路,表明 lncRNA 在致癌作用中发挥关键作用。当比较正常肺组织和吸烟者 LUAD 组织时,鉴定出 86 个候选基因,包括 6 个 lncRNA。在从不吸烟者 LUAD 组织和吸烟者 LUAD 组织之间比较时,揭示的 43 个候选基因中,有 13 个与正常肺组织也不同。然后,我们使用正常和肿瘤组织的基因表达 (GENT) 和正常和肿瘤组织的甲基化和表达数据库 (MENT) 数据库研究这些基因的表达。我们观察到正常肺组织和吸烟者 LUAD 组织中 13 个基因的表达呈负相关,从不吸烟者和吸烟者 LUAD 组织中 5 个基因的表达呈负相关。这些发现通过使用亚硫酸氢盐测序在临床标本中进一步验证,结果表明 AGR2、AURKB、FOXP3 和 HMGA1 的甲基化呈边缘差异。最后,我们探索了 DNA 甲基化、lncRNA 和基因表达之间的功能联系,以确定可能有助于吸烟相关 LUAD 发病机制的潜在靶点。总之,我们的研究结果表明,差异表达的 lncRNA 和它们的靶转录物可以作为 LUAD 的潜在生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c25/7939300/fc78037f6739/pone.0247928.g001.jpg

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