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A genomic case study of mixed fibrolamellar hepatocellular carcinoma.
Griffith, O L; Griffith, M; Krysiak, K; Magrini, V; Ramu, A; Skidmore, Z L; Kunisaki, J; Austin, R; McGrath, S; Zhang, J; Demeter, R; Graves, T; Eldred, J M; Walker, J; Larson, D E; Maher, C A; Lin, Y; Chapman, W; Mahadevan, A; Miksad, R; Nasser, I; Hanto, D W; Mardis, E R.
Afiliação
  • Griffith OL; McDonnell Genome Institute; Department of Medicine; Siteman Cancer Center; Department of Genetics. Electronic address: obigriffith@wustl.edu.
  • Griffith M; McDonnell Genome Institute; Siteman Cancer Center; Department of Genetics.
  • Krysiak K; McDonnell Genome Institute.
  • Magrini V; McDonnell Genome Institute; Department of Genetics.
  • Ramu A; McDonnell Genome Institute.
  • Skidmore ZL; McDonnell Genome Institute.
  • Kunisaki J; McDonnell Genome Institute.
  • Austin R; McDonnell Genome Institute.
  • McGrath S; McDonnell Genome Institute.
  • Zhang J; McDonnell Genome Institute.
  • Demeter R; McDonnell Genome Institute.
  • Graves T; McDonnell Genome Institute.
  • Eldred JM; McDonnell Genome Institute.
  • Walker J; McDonnell Genome Institute.
  • Larson DE; McDonnell Genome Institute; Department of Genetics.
  • Maher CA; McDonnell Genome Institute; Department of Medicine; Siteman Cancer Center.
  • Lin Y; Department of Surgery, Washington University School of Medicine, St Louis.
  • Chapman W; Department of Surgery, Washington University School of Medicine, St Louis.
  • Mahadevan A; Departments of Radiation Oncology.
  • Miksad R; Medicine.
  • Nasser I; Pathology, Harvard Medical School, Boston.
  • Hanto DW; Department of Surgery, Vanderbilt University School of Medicine, Nashville, USA.
  • Mardis ER; McDonnell Genome Institute; Department of Medicine; Siteman Cancer Center; Department of Genetics.
Ann Oncol ; 27(6): 1148-1154, 2016 06.
Article em En | MEDLINE | ID: mdl-27029710
BACKGROUND: Mixed fibrolamellar hepatocellular carcinoma (mFL-HCC) is a rare liver tumor defined by the presence of both pure FL-HCC and conventional HCC components, represents up to 25% of cases of FL-HCC, and has been associated with worse prognosis. Recent genomic characterization of pure FL-HCC identified a highly recurrent transcript fusion (DNAJB1:PRKACA) not found in conventional HCC. PATIENTS AND METHODS: We performed exome and transcriptome sequencing of a case of mFL-HCC. A novel BAC-capture approach was developed to identify a 400 kb deletion as the underlying genomic mechanism for a DNAJB1:PRKACA fusion in this case. A sensitive Nanostring Elements assay was used to screen for this transcript fusion in a second case of mFL-HCC, 112 additional HCC samples and 44 adjacent non-tumor liver samples. RESULTS: We report the first comprehensive genomic analysis of a case of mFL-HCC. No common HCC-associated mutations were identified. The very low mutation rate of this case, large number of mostly single-copy, long-range copy number variants, and high expression of ERBB2 were more consistent with previous reports of pure FL-HCC than conventional HCC. In particular, the DNAJB1:PRKACA fusion transcript specifically associated with pure FL-HCC was detected at very high expression levels. Subsequent analysis revealed the presence of this fusion in all primary and metastatic samples, including those with mixed or conventional HCC pathology. A second case of mFL-HCC confirmed our finding that the fusion was detectable in conventional components. An expanded screen identified a third case of fusion-positive HCC, which upon review, also had both conventional and fibrolamellar features. This screen confirmed the absence of the fusion in all conventional HCC and adjacent non-tumor liver samples. CONCLUSION: These results indicate that mFL-HCC is similar to pure FL-HCC at the genomic level and the DNAJB1:PRKACA fusion can be used as a diagnostic tool for both pure and mFL-HCC.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma Hepatocelular / Proteínas de Choque Térmico HSP40 / Subunidades Catalíticas da Proteína Quinase Dependente de AMP Cíclico / Neoplasias Hepáticas Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Adult / Female / Humans Idioma: En Revista: Ann Oncol Assunto da revista: NEOPLASIAS Ano de publicação: 2016 Tipo de documento: Article País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma Hepatocelular / Proteínas de Choque Térmico HSP40 / Subunidades Catalíticas da Proteína Quinase Dependente de AMP Cíclico / Neoplasias Hepáticas Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Adult / Female / Humans Idioma: En Revista: Ann Oncol Assunto da revista: NEOPLASIAS Ano de publicação: 2016 Tipo de documento: Article País de publicação: Reino Unido