Meta-analysis of global gene-expression profiles identify molecular signatures for histological subtypes of sarcomas

Zhiwei Qiao, Cuneyd Parlayan, Shigeru Saito, T. Kondo
{"title":"Meta-analysis of global gene-expression profiles identify molecular signatures for histological subtypes of sarcomas","authors":"Zhiwei Qiao, Cuneyd Parlayan, Shigeru Saito, T. Kondo","doi":"10.2198/JELECTROPH.62.21","DOIUrl":null,"url":null,"abstract":"SUMMARY Sarcomas are rare mesenchymal malignancies and comprise over 50 histological subtypes. Sarcomas are not well studied because the number of cases of individual sarcoma is low. The utilization of public data, such as gene expression data, may allow for improvement in the novel discovery of sarcoma. In this study, to gain insight into histological subtypes of sarcoma from a public database, we performed a meta-analysis of the gene-expression profiles by survey-ing the data deposited in the Gene Expression Omnibus database from 2001 to 2014. The gene-expression data for 10 sarcoma subtypes and the gene-expression profiles for 1002 cases were selected for comparative analysis. Genes with histology-oriented molecular signatures were identified, and the results were verified by functional validation using gene oncology analysis. Pathway analysis suggested the existence of differential biological processes among sarcoma subtypes. Furthermore, as an application of the sarcoma gene expression datasets used in this study, we investigated the gene expression patterns of the targets of pazopanib to predict the response of sarcoma to pazopanib. We found that the gene expression distribution patterns of targets of pazopanib were without distinction among 10 subtypes of sarcoma. Taken together, we identified the tissue-specific genes of 10 subtypes of sarcoma by bioinformatics analysis; our results demonstrated the utility of sarcoma datasets in public databases and provide valuable information for future rare cancer research.","PeriodicalId":15059,"journal":{"name":"Journal of capillary electrophoresis","volume":"53 1","pages":"21-29"},"PeriodicalIF":0.0000,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of capillary electrophoresis","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2198/JELECTROPH.62.21","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

SUMMARY Sarcomas are rare mesenchymal malignancies and comprise over 50 histological subtypes. Sarcomas are not well studied because the number of cases of individual sarcoma is low. The utilization of public data, such as gene expression data, may allow for improvement in the novel discovery of sarcoma. In this study, to gain insight into histological subtypes of sarcoma from a public database, we performed a meta-analysis of the gene-expression profiles by survey-ing the data deposited in the Gene Expression Omnibus database from 2001 to 2014. The gene-expression data for 10 sarcoma subtypes and the gene-expression profiles for 1002 cases were selected for comparative analysis. Genes with histology-oriented molecular signatures were identified, and the results were verified by functional validation using gene oncology analysis. Pathway analysis suggested the existence of differential biological processes among sarcoma subtypes. Furthermore, as an application of the sarcoma gene expression datasets used in this study, we investigated the gene expression patterns of the targets of pazopanib to predict the response of sarcoma to pazopanib. We found that the gene expression distribution patterns of targets of pazopanib were without distinction among 10 subtypes of sarcoma. Taken together, we identified the tissue-specific genes of 10 subtypes of sarcoma by bioinformatics analysis; our results demonstrated the utility of sarcoma datasets in public databases and provide valuable information for future rare cancer research.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
全球基因表达谱的荟萃分析确定了肉瘤组织学亚型的分子特征
肉瘤是一种罕见的间充质恶性肿瘤,包括50多种组织学亚型。由于单个肉瘤的病例数很少,因此对肉瘤的研究并不充分。利用公共数据,如基因表达数据,可能有助于改进肉瘤的新发现。在本研究中,为了从公共数据库中深入了解肉瘤的组织学亚型,我们通过调查2001年至2014年存放在Gene Expression Omnibus数据库中的数据,对基因表达谱进行了荟萃分析。选取10种肉瘤亚型的基因表达数据和1002例的基因表达谱进行对比分析。鉴定出具有组织学取向分子特征的基因,并通过基因肿瘤学分析进行功能验证。通路分析提示不同亚型肉瘤存在不同的生物学过程。此外,作为本研究中使用的肉瘤基因表达数据集的应用,我们研究了pazopanib靶点的基因表达模式,以预测肉瘤对pazopanib的反应。我们发现pazopanib靶点的基因表达分布模式在10种亚型肉瘤中没有区别。总之,我们通过生物信息学分析鉴定了10种肉瘤亚型的组织特异性基因;我们的研究结果证明了公共数据库中肉瘤数据集的实用性,并为未来的罕见癌症研究提供了有价值的信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Electrophoretic extraction of protein complexes after separation and detection by a combined method of non-denaturing two-dimensional electrophoresis and reversible staining Use of Escherichia coli expression system for analyzing kinase motifs Proteomic analysis of spheroids of rhabdomyosarcoma cells cultured with decellularized muscle extracts Drug screening and kinase activity profiling of a novel patient-derived cell line of clear cell ovarian carcinoma Proteogenomic approach to drug targets in osteosarcomas with different original sites
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1