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Article: Genome-wide identification of RNA editing in hepatocellular carcinoma

TitleGenome-wide identification of RNA editing in hepatocellular carcinoma
Authors
KeywordsHepatocellular carcinoma
RNA-editing
RNA-Seq
Issue Date2015
PublisherAcademic Press. The Journal's web site is located at http://www.elsevier.com/locate/ygeno
Citation
Genomics, 2015, v. 105 n. 2, p. 76-82 How to Cite?
AbstractWe did whole-transcriptome sequencing and whole-genome sequencing on nine pairs of Hepatocellular carcinoma (HCC) tumors and matched adjacent tissues to identify RNA editing events. We identified mean 26,982 editing sites with mean 89.5% canonical A→G edits in each sample using an improved bioinformatics pipeline. The editing rate was significantly higher in tumors than adjacent normal tissues. Comparing the difference between tumor and normal tissues of each patient, we found 7 non-synonymous tissue specific editing events including 4 tumor-specific edits and 3 normal-specific edits in the coding region, as well as 292 edits varying in editing degree. The significant expression changes of 150 genes associated with RNA editing were found in tumors, with 3 of the 4 most significant genes being cancer related. Our results show that editing might be related to higher gene expression. These findings indicate that RNA editing modification may play an important role in the development of HCC. Copyright © 2014 Elsevier Inc. All rights reserved.
Persistent Identifierhttp://hdl.handle.net/10722/207321
ISSN
2021 Impact Factor: 4.310
2020 SCImago Journal Rankings: 0.703
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorKang, L-
dc.contributor.authorLiu, X-
dc.contributor.authorGong, Z-
dc.contributor.authorZheng, H-
dc.contributor.authorWang, J-
dc.contributor.authorLi, Y-
dc.contributor.authorYang, H-
dc.contributor.authorHardwick, J-
dc.contributor.authorDai, H-
dc.contributor.authorPoon, RTP-
dc.contributor.authorLee, NPY-
dc.contributor.authorMao, M-
dc.contributor.authorPeng, Z-
dc.contributor.authorChen, R-
dc.date.accessioned2014-12-19T10:20:54Z-
dc.date.available2014-12-19T10:20:54Z-
dc.date.issued2015-
dc.identifier.citationGenomics, 2015, v. 105 n. 2, p. 76-82-
dc.identifier.issn0888-7543-
dc.identifier.urihttp://hdl.handle.net/10722/207321-
dc.description.abstractWe did whole-transcriptome sequencing and whole-genome sequencing on nine pairs of Hepatocellular carcinoma (HCC) tumors and matched adjacent tissues to identify RNA editing events. We identified mean 26,982 editing sites with mean 89.5% canonical A→G edits in each sample using an improved bioinformatics pipeline. The editing rate was significantly higher in tumors than adjacent normal tissues. Comparing the difference between tumor and normal tissues of each patient, we found 7 non-synonymous tissue specific editing events including 4 tumor-specific edits and 3 normal-specific edits in the coding region, as well as 292 edits varying in editing degree. The significant expression changes of 150 genes associated with RNA editing were found in tumors, with 3 of the 4 most significant genes being cancer related. Our results show that editing might be related to higher gene expression. These findings indicate that RNA editing modification may play an important role in the development of HCC. Copyright © 2014 Elsevier Inc. All rights reserved.-
dc.languageeng-
dc.publisherAcademic Press. The Journal's web site is located at http://www.elsevier.com/locate/ygeno-
dc.relation.ispartofGenomics-
dc.subjectHepatocellular carcinoma-
dc.subjectRNA-editing-
dc.subjectRNA-Seq-
dc.titleGenome-wide identification of RNA editing in hepatocellular carcinoma-
dc.typeArticle-
dc.identifier.emailPoon, RTP: poontp@hku.hk-
dc.identifier.emailLee, NPY: nikkilee@hku.hk-
dc.identifier.authorityPoon, RTP=rp00446-
dc.identifier.authorityLee, NPY=rp00263-
dc.identifier.doi10.1016/j.ygeno.2014.11.005-
dc.identifier.pmid25462863-
dc.identifier.scopuseid_2-s2.0-84922733768-
dc.identifier.hkuros241982-
dc.identifier.volume105-
dc.identifier.issue2-
dc.identifier.spage76-
dc.identifier.epage82-
dc.identifier.isiWOS:000348840200002-
dc.publisher.placeUnited States-
dc.identifier.issnl0888-7543-

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