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生发中心样弥漫性大B细胞淋巴瘤中长链非编码RNA的基因芯片表达谱

Microarray expression profiles of long non-coding RNAs in germinal center-like diffuse large B-cell lymphoma.

作者信息

Gao Hong-Yu, Wu Bin, Yan Wei, Gong Zi-Mu, Sun Qi, Wang Hui-Han, Yang Wei

机构信息

Department of Hematology, Shengjing Hospital of China Medical University, Tiexi, Shenyang, Liaoning 110000, P.R. China.

出版信息

Oncol Rep. 2017 Sep;38(3):1363-1372. doi: 10.3892/or.2017.5821. Epub 2017 Jul 14.

Abstract

Long non-coding RNAs (lncRNAs) are continuously transcribed and are involved in various cellular activities. However, their contributions to the occurrence and development of germinal center B-cell (GCB)-like diffuse large B-cell lymphoma (DLBCL) remain largely unknown. We applied microarray technology to profile the expression of lncRNAs in two different GCB-DLBCL cell lines (OCI-ly1 and OCI-ly19) and normal B lymphocytes. We demonstrated that 21,539 lncRNAs were expressed in all of the samples analyzed. This included 1,648 lncRNAs that showed a ≥2-fold upregulation and 2,671 lncRNAs that displayed a ≥2-fold downregulation in tumor cell lines (P<0.05). The expression levels of 8 lncRNAs were validated by quantitative reverse transcription polymerase chain reaction (qRT-PCR). Bioinformatic analyses (Gene Ontology, pathway and network analysis) were performed to predict how the differentially expressed lncRNAs may function in GCB-DLBCL. Results from the pathway analysis suggested that totals of 64 and 62 biological pathways corresponded to upregulated and downregulated transcripts, respectively (P<0.05). Additionally, we constructed a lncRNA‑mRNA network for the purpose of identifying specific coding genes which were co-expressed with 5 selected lncRNAs. Conclusively, our results may contribute to a better understanding of GCB-DLBCL pathogenesis.

摘要

长链非编码RNA(lncRNA)持续转录并参与多种细胞活动。然而,它们在生发中心B细胞(GCB)样弥漫性大B细胞淋巴瘤(DLBCL)发生和发展中的作用仍 largely unknown。我们应用微阵列技术分析了两种不同的GCB-DLBCL细胞系(OCI-ly1和OCI-ly19)及正常B淋巴细胞中lncRNA的表达情况。我们发现,在所有分析样本中均表达了21,539种lncRNA。其中,1,648种lncRNA在肿瘤细胞系中上调≥2倍,2,671种lncRNA下调≥2倍(P<0.05)。通过定量逆转录聚合酶链反应(qRT-PCR)验证了8种lncRNA的表达水平。进行了生物信息学分析(基因本体论、通路和网络分析),以预测差异表达的lncRNA在GCB-DLBCL中的可能功能。通路分析结果表明,分别有64条和62条生物学通路与上调和下调的转录本相对应(P<0.05)。此外,我们构建了一个lncRNA-mRNA网络,以鉴定与5种选定lncRNA共表达的特定编码基因。总之,我们的结果可能有助于更好地理解GCB-DLBCL的发病机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32bc/5549037/1f8e332f6bfe/OR-38-03-1363-g00.jpg

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