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RNA Sequencing of Hepatobiliary Cancer Cell Lines: Data and Applications to Mutational and Transcriptomic Profiling.
Scherer, Dominique; Dávila López, Marcela Dávila; Goeppert, Benjamin; Abrahamsson, Sanna; González Silos, Rosa González; Nova, Igor; Marcelain, Katherine; Roa, Juan C; Ibberson, David; Umu, Sinan U; Rounge, Trine Ballestad; Roessler, Stephanie; Bermejo, Justo Lorenzo.
Afiliação
  • Scherer D; Institute of Medical Biometry and Informatics, University of Heidelberg, 69120 Heidelberg, Germany.
  • Dávila López MD; Bioinformatics Core Facility, University of Gothenburg, 40530 Gothenburg, Sweden.
  • Goeppert B; Institute of Pathology, Heidelberg University Hospital, 69120 Heidelberg, Germany.
  • Abrahamsson S; Bioinformatics Core Facility, University of Gothenburg, 40530 Gothenburg, Sweden.
  • González Silos RG; Institute of Medical Biometry and Informatics, University of Heidelberg, 69120 Heidelberg, Germany.
  • Nova I; Institute of Medical Biometry and Informatics, University of Heidelberg, 69120 Heidelberg, Germany.
  • Marcelain K; Department of Basic and Clinical Oncology, Faculty of Medicine, Universidad ode Chile, Santiago 8380000, Chile.
  • Roa JC; Department of Pathology, Faculty of Medicine, Millennium Institute of Immunology and Immunotherapy, Pontificia Universidad Católica de Chile, Santiago 8330024, Chile.
  • Ibberson D; Deep Sequencing Core Facility, CellNetworks Excellence Cluster, University of Heidelberg, 69120 Heidelberg, Germany.
  • Umu SU; Department of Research, Cancer Registry of Norway, 0379 Oslo, Norway.
  • Rounge TB; Department of Research, Cancer Registry of Norway, 0379 Oslo, Norway.
  • Roessler S; Department of Informatics, University of Oslo, 0373 Oslo, Norway.
  • Bermejo JL; Institute of Pathology, Heidelberg University Hospital, 69120 Heidelberg, Germany.
Cancers (Basel) ; 12(9)2020 Sep 03.
Article em En | MEDLINE | ID: mdl-32899426
ABSTRACT
Cancer cell lines allow the identification of clinically relevant alterations and the prediction of drug response. However, sequencing data for hepatobiliary cancer cell lines in general, and particularly gallbladder cancer (GBC), are sparse. Here, we apply RNA sequencing to characterize 10 GBC, eight hepatocellular carcinoma, and five cholangiocarcinoma (CCA) cell lines. RNA extraction, quality control, library preparation, sequencing, and pre-processing of sequencing data were implemented using state-of-the-art techniques. Public data from the MSK-IMPACT database and a large cohort of Japanese biliary tract cancer patients were used to illustrate the usage of the released data. The total number of exonic mutations varied from 7207 for the cell line NOZ to 9760 for HuCCT1. Researchers planning experiments that require TP53 mutations could use the cell lines NOZ, OCUG-1, SNU308, or YoMi. Mz-Cha-1 showed mutations in ATM, SNU308 presented SMAD4 mutations, and the only investigated cell line that showed ARID1A mutations was GB-d1. SNU478 was the cell line with the global gene expression pattern most similar to GBC, intrahepatic CCA, and extrahepatic CCA. EGFR, KMT2D, and KMT2C generally presented a higher expression in the investigated cell lines than in Japanese primary GBC tumors. We provide the scientific community with detailed mutation and gene expression data, together with three showcase applications, with the aim of facilitating the design of future in vitro cell culture assays for research on hepatobiliary cancer.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article