中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Long non-coding RNA expression profiles of hepatitis C virus-related dysplasia and hepatocellular carcinoma

文献类型:期刊论文

作者Zhang, Haohai1,5; Zhu, Chengpei1,5; Zhao, Yi3,4; Li, Ming2; Wu, Liangcai1,5; Yang, Xiaobo1,5; Wan, Xueshuai1,5; Wang, Anqiang1,5; Zhang, Michael Q.1,3,4,5; Sang, Xinting1,5
刊名ONCOTARGET
出版日期2015-12-22
卷号6期号:41页码:43770-43778
关键词long non-coding RNAs hepatitis C virus-refafed HCC hepafocarcinogenfc process biomarkers
ISSN号1949-2553
英文摘要Recently, long non-coding RNAs (IncRNAs) were found to be implicated in cancer progression. However, the contributions of IncRNAs to Hepatitis C virus-related hepatocellular carcinoma (HCC) remain largely unknown. Here, we characterized IncRNA expression in 73 tissue samples from several different developmental stages of HCV-related hepatocarcinogenesis by repurposing microarray data sets. We found that the expression of 7 IncRNAs in preneoplastic lesions and HCC was significantly different. Among these significantly differently expressed IncRNAs, the IncRNA LINC01419 transcripts were expressed at higher levels in early stage HCC compared to dysplasia and as compared with early stage HCC, IncRNA AK021443 level increase in advanced stage HCC while IncRNA AF070632 level decrease in advanced stage HCC. Using quantitative real-time reverse-transcription PCR, we validated that LINC01419 was significantly overexpressed in HBV-related and HCV-related HCC when compared with matched non-tumor liver tissues. Moreover, functional predictions suggested that LINC01419 and AK021443 regulate cell cycle genes, whereas AF070632 is associated with cofactor binding, oxidation-reduction and carboxylic acid catabolic process. These findings provide the first large-scale survey of IncRNAs associated with the development of hepatocarcinogenesis and may offer new diagnostic biomarkers and therapeutic targets for HCV-related HCC.
资助项目International Science and Technology Cooperation Projects[2015DFA30650] ; International Science and Technology Cooperation Projects[2010DFB33720] ; Capital Special Research Project for Health Development[2014-2-4012] ; Capital Research Project for the Characteristics Clinical application[Z151100004015170] ; Program for New Program for New Century Excellent Talents in University[NCET-11-0288]
WOS研究方向Oncology ; Cell Biology
语种英语
WOS记录号WOS:000369908400045
出版者IMPACT JOURNALS LLC
源URL[http://119.78.100.204/handle/2XEOYT63/8722]  
专题中国科学院计算技术研究所期刊论文_英文
通讯作者Zhao, Haitao
作者单位1.Chinese Acad Med Sci, Peking Union Med Coll Hosp, Dept Liver Surg, Beijing 100730, Peoples R China
2.Chinese Acad Sci, Inst Comp Technol, Key Lab Intelligent Informat Proc, Beijing, Peoples R China
3.Tsinghua Univ, Ctr Synthet & Syst Biol, Bioinformat Div, Beijing 100084, Peoples R China
4.Tsinghua Univ, Sch Med, MOE Key Lab Bioinformat, Beijing 100084, Peoples R China
5.Peking Union Med Coll, Beijing 100021, Peoples R China
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Zhang, Haohai,Zhu, Chengpei,Zhao, Yi,et al. Long non-coding RNA expression profiles of hepatitis C virus-related dysplasia and hepatocellular carcinoma[J]. ONCOTARGET,2015,6(41):43770-43778.
APA Zhang, Haohai.,Zhu, Chengpei.,Zhao, Yi.,Li, Ming.,Wu, Liangcai.,...&Zhao, Haitao.(2015).Long non-coding RNA expression profiles of hepatitis C virus-related dysplasia and hepatocellular carcinoma.ONCOTARGET,6(41),43770-43778.
MLA Zhang, Haohai,et al."Long non-coding RNA expression profiles of hepatitis C virus-related dysplasia and hepatocellular carcinoma".ONCOTARGET 6.41(2015):43770-43778.

入库方式: OAI收割

来源:计算技术研究所

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