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Genome-wide identification of RNA editing in hepatocellular carcinoma.
Kang, Lin; Liu, Xiaoqiao; Gong, Zhoulin; Zheng, Hancheng; Wang, Jun; Li, Yingrui; Yang, Huanming; Hardwick, James; Dai, Hongyue; Poon, Ronnie T P; Lee, Nikki P; Mao, Mao; Peng, Zhiyu; Chen, Ronghua.
Affiliation
  • Kang L; BGI-Shenzhen, Shenzhen, China. Electronic address: kanglinxm@gmail.com.
  • Liu X; Scientific Informatics, MSD R&D (China), Beijing, China. Electronic address: xiao.qiao.liu@merck.com.
  • Gong Z; BGI-Shenzhen, Shenzhen, China; BGI-Tech, BGI-Shenzhen, Shenzhen, China. Electronic address: gongzhuolin@bgitechsolutions.com.
  • Zheng H; BGI-Shenzhen, Shenzhen, China; BGI-Tech, BGI-Shenzhen, Shenzhen, China. Electronic address: zhenghch@genomics.cn.
  • Wang J; BGI-Shenzhen, Shenzhen, China; King Abdulaziz University Jeddah, Saudi Arabia; Department of Biology, University of Copenhagen, Copenhagen, Denmark. Electronic address: wangj@genomics.org.cn.
  • Li Y; BGI-Shenzhen, Shenzhen, China; BGI-Tech, BGI-Shenzhen, Shenzhen, China. Electronic address: liyr@genomics.org.cn.
  • Yang H; BGI-Shenzhen, Shenzhen, China; King Abdulaziz University Jeddah, Saudi Arabia; James D. Watson Institute of Genome Science, Hangzhou, China. Electronic address: yanghm@genomics.cn.
  • Hardwick J; Merck Research Laboratories, Merck & Co., Inc., Boston, MA, USA. Electronic address: james_hardwick@merck.com.
  • Dai H; Merck Research Laboratories, Merck & Co., Inc., Boston, MA, USA. Electronic address: hongyue_dai@merck.com.
  • Poon RT; Department of Surgery, The University of Hong Kong, Hong Kong. Electronic address: poontp@hkucc.hku.hk.
  • Lee NP; Department of Surgery, The University of Hong Kong, Hong Kong. Electronic address: nikkilee@hku.hk.
  • Mao M; Pfizer Oncology, San Diego, CA, USA; Asian Cancer Research Group, Inc., Wilmington, DE, USA. Electronic address: mao_m@yahoo.com.
  • Peng Z; BGI-Shenzhen, Shenzhen, China; Guangzhou Key Laboratory of Cancer Trans-Omics Research, BGI-Guangzhou, Guangzhou, China. Electronic address: pengzhiyu@genomics.cn.
  • Chen R; Scientific Informatics, MSD R&D (China), Beijing, China; Scientific Informatics, Merck & Co., Inc., Boston, MA, USA. Electronic address: ronghua_chen@merck.com.
Genomics ; 105(2): 76-82, 2015 Feb.
Article in En | MEDLINE | ID: mdl-25462863
ABSTRACT
We 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.
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Full text: 1 Database: MEDLINE Main subject: Genome / RNA Editing / Carcinoma, Hepatocellular / Transcriptome / Liver Neoplasms Type of study: Diagnostic_studies / Prognostic_studies Limits: Humans Language: En Year: 2015 Type: Article

Full text: 1 Database: MEDLINE Main subject: Genome / RNA Editing / Carcinoma, Hepatocellular / Transcriptome / Liver Neoplasms Type of study: Diagnostic_studies / Prognostic_studies Limits: Humans Language: En Year: 2015 Type: Article