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肝细胞癌基因表达谱的生物信息学分析:初步结果

Bioinformatics analysis of the gene expression profile of hepatocellular carcinoma: preliminary results.

作者信息

Li Jia, Huang Zhongxi, Wei Lixin

机构信息

Department of Pathology, Chinese PLA General Hospital, Beijing, China; Medical College, Nankai University, Tianjing, China.

Institute of Oncology, Nanfang Medical University, Guangzhou, Guangdong, China.

出版信息

Contemp Oncol (Pozn). 2016;20(1):20-7. doi: 10.5114/wo.2016.58497. Epub 2016 Mar 16.

Abstract

AIM OF THE STUDY

To analyse the expression profile of hepatocellular carcinoma compared with normal liver by using bioinformatics methods.

MATERIAL AND METHODS

In this study, we analysed the microarray expression data of HCC and adjacent normal liver samples from the Gene Expression Omnibus (GEO) database to screen for differentially expressed genes. Then, functional analyses were performed using GenCLiP analysis, Gene Ontology categories, and aberrant pathway identification. In addition, we used the CMap database to identify small molecules that can induce HCC.

RESULTS

Overall, 2721 differentially expressed genes (DEGs) were identified. We found 180 metastasis-related genes and constructed co-occurrence networks. Several significant pathways, including the transforming growth factor β (TGF-β) signalling pathway, were identified as closely related to these DEGs. Some candidate small molecules (such as betahistine) were identified that might provide a basis for developing HCC treatments in the future.

CONCLUSIONS

Although we functionally analysed the differences in the gene expression profiles of HCC and normal liver tissues, our study is essentially preliminary, and it may be premature to apply our results to clinical trials. Further research and experimental testing are required in future studies.

摘要

研究目的

运用生物信息学方法分析肝细胞癌与正常肝脏相比的表达谱。

材料与方法

在本研究中,我们分析了来自基因表达综合数据库(GEO)的肝癌及相邻正常肝脏样本的微阵列表达数据,以筛选差异表达基因。然后,使用GenCLiP分析、基因本体类别和异常通路识别进行功能分析。此外,我们使用CMap数据库来识别可诱导肝癌的小分子。

结果

总体而言,共鉴定出2721个差异表达基因(DEG)。我们发现了180个转移相关基因并构建了共现网络。包括转化生长因子β(TGF-β)信号通路在内的几个重要通路被确定与这些DEG密切相关。鉴定出了一些候选小分子(如倍他司汀),这可能为未来肝癌治疗的开发提供基础。

结论

尽管我们对肝癌和正常肝脏组织的基因表达谱差异进行了功能分析,但我们的研究本质上是初步的,将我们的结果应用于临床试验可能为时过早。未来的研究需要进一步的研究和实验测试。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e2e7/4829745/f8c333771fda/WO-20-27106-g001.jpg

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