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Genomic distinctions between metastatic lower and upper tract urothelial carcinoma revealed through rapid autopsy.
Winters, Brian R; De Sarkar, Navonil; Arora, Sonali; Bolouri, Hamid; Jana, Sujata; Vakar-Lopez, Funda; Cheng, Heather H; Schweizer, Michael T; Yu, Evan Y; Grivas, Petros; Lee, John K; Kollath, Lori; Holt, Sarah K; McFerrin, Lisa; Ha, Gavin; Nelson, Peter S; Montgomery, Robert B; Wright, Jonathan L; Lam, Hung-Ming; Hsieh, Andrew C.
Afiliação
  • Winters BR; Department of Urology and.
  • De Sarkar N; Department of Medicine, Division of Oncology, University of Washington School of Medicine, Seattle, Washington, USA.
  • Arora S; Division of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
  • Bolouri H; Division of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
  • Jana S; Division of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
  • Vakar-Lopez F; Division of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
  • Cheng HH; Department of Pathology, University of Washington School of Medicine, Seattle, Washington, USA.
  • Schweizer MT; Department of Medicine, Division of Oncology, University of Washington School of Medicine, Seattle, Washington, USA.
  • Yu EY; Department of Medicine, Division of Oncology, University of Washington School of Medicine, Seattle, Washington, USA.
  • Grivas P; Department of Medicine, Division of Oncology, University of Washington School of Medicine, Seattle, Washington, USA.
  • Lee JK; Department of Medicine, Division of Oncology, University of Washington School of Medicine, Seattle, Washington, USA.
  • Kollath L; Department of Medicine, Division of Oncology, University of Washington School of Medicine, Seattle, Washington, USA.
  • Holt SK; Division of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
  • McFerrin L; Department of Urology and.
  • Ha G; Department of Urology and.
  • Nelson PS; Division of Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
  • Montgomery RB; Division of Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
  • Wright JL; Department of Medicine, Division of Oncology, University of Washington School of Medicine, Seattle, Washington, USA.
  • Lam HM; Division of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
  • Hsieh AC; Department of Medicine, Division of Oncology, University of Washington School of Medicine, Seattle, Washington, USA.
JCI Insight ; 52019 05 30.
Article em En | MEDLINE | ID: mdl-31145100
BACKGROUND: Little is known about the genomic differences between metastatic urothelial carcinoma (LTUC) and upper tract urothelial carcinoma (UTUC). We compare genomic features of primary and metastatic UTUC and LTUC tumors in a cohort of patients with end stage disease. METHODS: We performed whole exome sequencing on matched primary and metastatic tumor samples (N=37) from 7 patients with metastatic UC collected via rapid autopsy. Inter- and intra-patient mutational burden, mutational signatures, predicted deleterious mutations, and somatic copy alterations (sCNV) were analyzed. RESULTS: We investigated 3 patients with UTUC (3 primary samples, 13 metastases) and 4 patients with LTUC (4 primary samples, 17 metastases). We found that sSNV burden was higher in metastatic LTUC compared to UTUC. Moreover, the APOBEC mutational signature was pervasive in metastatic LTUC and less so in UTUC. Despite a lower overall sSNV burden, UTUC displayed greater inter- and intra-individual genomic distances at the copy number level between primary and metastatic tumors than LTUC. Our data also indicate that metastatic UTUC lesions can arise from small clonal populations present in the primary cancer. Importantly, putative druggable mutations were found across patients with the majority shared across all metastases within a patient. CONCLUSIONS: Metastatic UTUC demonstrated a lower overall mutational burden but greater structural variability compared to LTUC. Our findings suggest that metastatic UTUC displays a greater spectrum of copy number divergence from LTUC. Importantly, we identified druggable lesions shared across metastatic samples, which demonstrate a level of targetable homogeneity within individual patients.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma de Células de Transição / Neoplasias Urológicas / Genômica Tipo de estudo: Prognostic_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: JCI Insight Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma de Células de Transição / Neoplasias Urológicas / Genômica Tipo de estudo: Prognostic_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: JCI Insight Ano de publicação: 2019 Tipo de documento: Article