Identification of Liver Cancer Stem Cell Stemness Markers Using a Comparative Analysis of Public Data Sets.

IF 1.7 Q4 CELL BIOLOGY
Stem Cells and Cloning-Advances and Applications Pub Date : 2021-06-16 eCollection Date: 2021-01-01 DOI:10.2147/SCCAA.S307043
Kirill Borziak, Joseph Finkelstein
{"title":"Identification of Liver Cancer Stem Cell Stemness Markers Using a Comparative Analysis of Public Data Sets.","authors":"Kirill Borziak,&nbsp;Joseph Finkelstein","doi":"10.2147/SCCAA.S307043","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>Comparative reanalysis of single-cell transcriptomics data to gain useful novel insights into cancer stem cells (CSCs), which are a rare subset of cells within tumors, characterized by their capability to self-renew and differentiate, and their role in tumorigenicity.</p><p><strong>Patients and methods: </strong>This project utilized publically available liver single-cell RNA-seq datasets of liver cancer and liver progenitor cell types to demonstrate how shared large amounts of data can generate new and valuable information. The data were analyzed using EdgeR differential expression analysis, with focus on a set of 34 known stemness markers.</p><p><strong>Results: </strong>We showed that the expression of stemness markers SOX9, KRT19, KRT7, and CD24, and Yamanaka factors Oct4 and SOX2 in CSCs was significantly elevated relative to progenitor cell types, potentially explaining their increased differentiation and replication potential.</p><p><strong>Conclusion: </strong>These results help to further document the complementary expression changes that give CSCs their distinct phenotypic profile. Our findings have potential significance to advance our knowledge of the important genes relevant to CSCs.</p>","PeriodicalId":44934,"journal":{"name":"Stem Cells and Cloning-Advances and Applications","volume":"14 ","pages":"9-17"},"PeriodicalIF":1.7000,"publicationDate":"2021-06-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/2a/a0/sccaa-14-9.PMC8216768.pdf","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Stem Cells and Cloning-Advances and Applications","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2147/SCCAA.S307043","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2021/1/1 0:00:00","PubModel":"eCollection","JCR":"Q4","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 3

Abstract

Purpose: Comparative reanalysis of single-cell transcriptomics data to gain useful novel insights into cancer stem cells (CSCs), which are a rare subset of cells within tumors, characterized by their capability to self-renew and differentiate, and their role in tumorigenicity.

Patients and methods: This project utilized publically available liver single-cell RNA-seq datasets of liver cancer and liver progenitor cell types to demonstrate how shared large amounts of data can generate new and valuable information. The data were analyzed using EdgeR differential expression analysis, with focus on a set of 34 known stemness markers.

Results: We showed that the expression of stemness markers SOX9, KRT19, KRT7, and CD24, and Yamanaka factors Oct4 and SOX2 in CSCs was significantly elevated relative to progenitor cell types, potentially explaining their increased differentiation and replication potential.

Conclusion: These results help to further document the complementary expression changes that give CSCs their distinct phenotypic profile. Our findings have potential significance to advance our knowledge of the important genes relevant to CSCs.

Abstract Image

Abstract Image

Abstract Image

利用公共数据集的比较分析鉴定肝癌干细胞干性标记。
目的:对单细胞转录组学数据进行比较再分析,以获得对肿瘤干细胞(CSCs)有用的新见解,CSCs是肿瘤内罕见的细胞亚群,其特点是具有自我更新和分化的能力,以及它们在致瘤性中的作用。患者和方法:该项目利用公开的肝癌和肝祖细胞类型的肝脏单细胞RNA-seq数据集来展示共享的大量数据如何产生新的和有价值的信息。使用EdgeR差异表达分析对数据进行分析,重点关注一组34个已知的干性标记。结果:我们发现干细胞中的干性标记SOX9、KRT19、KRT7和CD24以及Yamanaka因子Oct4和SOX2的表达相对于祖细胞类型显著升高,这可能解释了它们增加分化和复制潜力的原因。结论:这些结果有助于进一步记录互补表达的变化,使csc具有独特的表型特征。我们的发现对我们进一步了解与csc相关的重要基因具有潜在的意义。
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 求助全文
来源期刊
CiteScore
6.50
自引率
0.00%
发文量
10
审稿时长
16 weeks
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信