Department of Clinical Laboratory, Liaocheng People's Hospital, Liaocheng, PR China.
Department of Neurology First Ward, Liaocheng Veterans Hospital, Liaocheng, PR China.
Epigenomics. 2021 Jul;13(14):1113-1128. doi: 10.2217/epi-2021-0152. Epub 2021 Jun 21.
To delineate the transcriptomic landscape and potential molecular mechanisms of breast cancer brain metastasis (BCBM). Whole-transcriptome sequencing was performed to identify long noncoding RNA (lncRNA), miRNA and mRNA expression profiles associated with BCBM. A total of 739 differentially expressed lncRNAs, 115 differentially expressed miRNAs and 5749 differentially expressed mRNAs were identified in 231-BR cells compared with MDA-MB-231 cells. Real-time quantitative PCR results revealed the expression levels of candidate molecules were consistent with their correspondence RNA-seq data. Protein-protein interaction analysis identified some hub genes associated with BCBM, such as , and . LncRNA-miRNA-mRNA network highlighted a potential mechanism of BCBM in which lncRNA and RP11-169F17.1 sponging hsa-miR-501-5p to regulate the expression of , and . This study provides a framework for better understanding molecular mechanisms of BCBM.
为了描绘乳腺癌脑转移(BCBM)的转录组景观和潜在分子机制。我们进行了全转录组测序,以鉴定与 BCBM 相关的长非编码 RNA(lncRNA)、miRNA 和 mRNA 表达谱。与 MDA-MB-231 细胞相比,在 231-BR 细胞中鉴定出了 739 个差异表达的 lncRNA、115 个差异表达的 miRNA 和 5749 个差异表达的 mRNA。实时定量 PCR 结果显示候选分子的表达水平与其相应的 RNA-seq 数据一致。蛋白质-蛋白质相互作用分析鉴定出了一些与 BCBM 相关的关键基因,如、和。lncRNA-miRNA-mRNA 网络突出了 BCBM 的一个潜在机制,其中 lncRNA 和 RP11-169F17.1 作为 hsa-miR-501-5p 的海绵,调节的表达。本研究为更好地理解 BCBM 的分子机制提供了一个框架。