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Generation of Whole-Genome Sequencing Data for Comparing Primary and Castration-Resistant Prostate Cancer

  • Park, Jong-Lyul (Genome Editing Research Center, Korea Research Institute of Bioscience and Biotechnology) ;
  • Kim, Seon-Kyu (Personalized Genomic Medicine Research Center, Korea Research Institute of Bioscience and Biotechnology) ;
  • Kim, Jeong-Hwan (Genome Editing Research Center, Korea Research Institute of Bioscience and Biotechnology) ;
  • Yun, Seok Joong (Department of Urology, Chungbuk National University College of Medicine) ;
  • Kim, Wun-Jae (Department of Urology, Chungbuk National University College of Medicine) ;
  • Kim, Won Tae (Department of Urology, Chungbuk National University College of Medicine) ;
  • Jeong, Pildu (Department of Urology, Chungbuk National University College of Medicine) ;
  • Kang, Ho Won (Department of Urology, Chungbuk National University Hospital) ;
  • Kim, Seon-Young (Genome Editing Research Center, Korea Research Institute of Bioscience and Biotechnology)
  • Received : 2018.05.08
  • Accepted : 2018.06.15
  • Published : 2018.09.30

Abstract

Because castration-resistant prostate cancer (CRPC) does not respond to androgen deprivation therapy and has a very poor prognosis, it is critical to identify a prognostic indicator for predicting high-risk patients who will develop CRPC. Here, we report a dataset of whole genomes from four pairs of primary prostate cancer (PC) and CRPC samples. The analysis of the paired PC and CRPC samples in the whole-genome data showed that the average number of somatic mutations per patients was 7,927 in CRPC tissues compared with primary PC tissues (range, 1,691 to 21,705). Our whole-genome sequencing data of primary PC and CRPC may be useful for understanding the genomic changes and molecular mechanisms that occur during the progression from PC to CRPC.

Keywords

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