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微小RNA表达谱分析鉴定非小细胞肺癌的新型生物标志物。

Analysis of microRNA expression profile identifies novel biomarkers for non-small cell lung cancer.

作者信息

Xu Chi, Zheng Yisheng, Lian Duohuang, Ye Shixin, Yang Jinrong, Zeng Zhiyong

出版信息

Tumori. 2015 Jan-Feb;101(1):104-10. doi: 10.5301/tj.5000224.

Abstract

BACKGROUND

Non-small cell lung cancer (NSCLC) is one of the leading causes of cancer mortality. MicroRNAs (miRNAs), small noncoding RNAs, regulate the expression of genes that play roles in human cancer via posttranscriptional inhibition.

METHODS

To identify the potential miRNA biomarkers in NSCLC, we downloaded the miRNA expression profile (ID: GSE29248) of NSCLC from the Gene Expression Omnibus (GEO) database and analyzed the differentially expressed miRNAs in NSCLC tissue compared with normal control tissue. Then the targets of these differentially expressed miRNAs were screened and used in network construction and functional enrichment analysis.

RESULTS

We identified a total of 17 miRNAs that showed a significantly differential expression in NSCLC tissue. We found that miR-34b and miR-520h might play important roles in the regulation of NSCLC, miR-22 might be a novel biomarker as an oncogene, and miR-448 might promote, while miR-654-3p prevents, NSCLC progression.

CONCLUSIONS

Our study may provide the groundwork for further clinical molecular target therapy experiments in NSCLC.BAC

摘要

背景

非小细胞肺癌(NSCLC)是癌症死亡的主要原因之一。微小RNA(miRNA)是一类小的非编码RNA,通过转录后抑制作用调节在人类癌症中起作用的基因的表达。

方法

为了鉴定NSCLC中潜在的miRNA生物标志物,我们从基因表达综合数据库(GEO)下载了NSCLC的miRNA表达谱(ID:GSE29248),并分析了NSCLC组织与正常对照组织中差异表达的miRNA。然后筛选这些差异表达miRNA的靶标,并用于网络构建和功能富集分析。

结果

我们共鉴定出17种在NSCLC组织中表现出显著差异表达的miRNA。我们发现miR-34b和miR-520h可能在NSCLC的调控中起重要作用,miR-22作为一种癌基因可能是一种新型生物标志物,miR-448可能促进NSCLC进展,而miR-654-3p则阻止NSCLC进展。

结论

我们的研究可能为NSCLC进一步的临床分子靶向治疗实验提供基础。

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