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使用独立数据集的表达数据验证 miRNA 在肝细胞癌中的预后能力。

Validation of miRNA prognostic power in hepatocellular carcinoma using expression data of independent datasets.

机构信息

MTA TTK Lendület Cancer Biomarker Research Group, Institute of Enzymology, Magyar Tudósok körútja 2, 1117, Budapest, Hungary.

Semmelweis University 2nd Dept. of Pediatrics, Tűzoltó utca 7-9, 1094, Budapest, Hungary.

出版信息

Sci Rep. 2018 Jun 15;8(1):9227. doi: 10.1038/s41598-018-27521-y.

DOI:10.1038/s41598-018-27521-y
PMID:29907753
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6003936/
Abstract

Multiple studies suggested using different miRNAs as biomarkers for prognosis of hepatocellular carcinoma (HCC). We aimed to assemble a miRNA expression database from independent datasets to enable an independent validation of previously published prognostic biomarkers of HCC. A miRNA expression database was established by searching the TCGA (RNA-seq) and GEO (microarray) repositories to identify miRNA datasets with available expression and clinical data. A PubMed search was performed to identify prognostic miRNAs for HCC. We performed a uni- and multivariate Cox regression analysis to validate the prognostic significance of these miRNAs. The Limma R package was applied to compare the expression of miRNAs between tumor and normal tissues. We uncovered 214 publications containing 223 miRNAs identified as potential prognostic biomarkers for HCC. In the survival analysis, the expression levels of 55 and 84 miRNAs were significantly correlated with overall survival in RNA-seq and gene chip datasets, respectively. The most significant miRNAs were hsa-miR-149, hsa-miR-139, and hsa-miR-3677 in the RNA-seq and hsa-miR-146b-3p, hsa-miR-584, and hsa-miR-31 in the microarray dataset. Of the 223 miRNAs studied, the expression was significantly altered in 102 miRNAs in tumors compared to normal liver tissues. In summary, we set up an integrated miRNA expression database and validated prognostic miRNAs in HCC.

摘要

多项研究表明,使用不同的 miRNA 作为肝细胞癌 (HCC) 预后的生物标志物。我们旨在从独立数据集组装 miRNA 表达数据库,以实现对 HCC 先前发表的预后生物标志物的独立验证。通过搜索 TCGA(RNA-seq)和 GEO(微阵列)存储库来建立 miRNA 表达数据库,以识别具有可用表达和临床数据的 miRNA 数据集。进行 PubMed 搜索以识别 HCC 的预后 miRNA。我们进行了单变量和多变量 Cox 回归分析,以验证这些 miRNA 的预后意义。应用 Limma R 软件包比较肿瘤和正常组织中 miRNA 的表达。我们发现了 214 篇包含 223 个 miRNA 的出版物,这些 miRNA 被确定为 HCC 潜在的预后生物标志物。在生存分析中,RNA-seq 和基因芯片数据集中分别有 55 和 84 个 miRNA 的表达水平与总生存期显著相关。RNA-seq 中最显著的 miRNA 是 hsa-miR-149、hsa-miR-139 和 hsa-miR-3677,而在微阵列数据集中最显著的 miRNA 是 hsa-miR-146b-3p、hsa-miR-584 和 hsa-miR-31。在研究的 223 个 miRNA 中,与正常肝组织相比,肿瘤中有 102 个 miRNA 的表达明显改变。总之,我们建立了一个综合的 miRNA 表达数据库,并验证了 HCC 中的预后 miRNA。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8121/6003936/db18a5c3fe0d/41598_2018_27521_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8121/6003936/74c049392ea8/41598_2018_27521_Fig1_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8121/6003936/b9078f5b22b6/41598_2018_27521_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8121/6003936/b3744c80ff15/41598_2018_27521_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8121/6003936/db18a5c3fe0d/41598_2018_27521_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8121/6003936/74c049392ea8/41598_2018_27521_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8121/6003936/13efb218a047/41598_2018_27521_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8121/6003936/a16367cd30cd/41598_2018_27521_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8121/6003936/b9078f5b22b6/41598_2018_27521_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8121/6003936/b3744c80ff15/41598_2018_27521_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8121/6003936/db18a5c3fe0d/41598_2018_27521_Fig6_HTML.jpg

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