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Genomic and signalling pathway characterization of the NZM panel of melanoma cell lines: A valuable model for studying the impact of genetic diversity in melanoma.
Tran, Khanh B; Gimenez, Gregory; Tsai, Peter; Kolekar, Sharada; Rodger, Euan J; Chatterjee, Aniruddha; Jabed, Anower; Shih, Jen-Hsing; Joseph, Wayne R; Marshall, Elaine S; Wang, Qian; Print, Cristin G; Eccles, Michael R; Baguley, Bruce C; Shepherd, Peter R.
Afiliação
  • Tran KB; Department of Molecular Medicine and Pathology, University of Auckland, Auckland, New Zealand.
  • Gimenez G; Maurice Wilkins Centre for Molecular Biodiscovery, Auckland, New Zealand.
  • Tsai P; Maurice Wilkins Centre for Molecular Biodiscovery, Auckland, New Zealand.
  • Kolekar S; Department of Pathology, Dunedin School of Medicine, University of Otago, Dunedin, New Zealand.
  • Rodger EJ; Department of Molecular Medicine and Pathology, University of Auckland, Auckland, New Zealand.
  • Chatterjee A; Department of Molecular Medicine and Pathology, University of Auckland, Auckland, New Zealand.
  • Jabed A; Auckland Cancer Society Research Centre, University of Auckland, Auckland, New Zealand.
  • Shih JH; Maurice Wilkins Centre for Molecular Biodiscovery, Auckland, New Zealand.
  • Joseph WR; Department of Pathology, Dunedin School of Medicine, University of Otago, Dunedin, New Zealand.
  • Marshall ES; Maurice Wilkins Centre for Molecular Biodiscovery, Auckland, New Zealand.
  • Wang Q; Department of Pathology, Dunedin School of Medicine, University of Otago, Dunedin, New Zealand.
  • Print CG; Department of Molecular Medicine and Pathology, University of Auckland, Auckland, New Zealand.
  • Eccles MR; Department of Molecular Medicine and Pathology, University of Auckland, Auckland, New Zealand.
  • Baguley BC; Auckland Cancer Society Research Centre, University of Auckland, Auckland, New Zealand.
  • Shepherd PR; Auckland Cancer Society Research Centre, University of Auckland, Auckland, New Zealand.
Pigment Cell Melanoma Res ; 34(1): 136-143, 2021 01.
Article em En | MEDLINE | ID: mdl-32567790
ABSTRACT
Melanoma is a disease associated with a very high mutation burden and thus the possibility of a diverse range of oncogenic mechanisms that allow it to evade therapeutic interventions and the immune system. Here, we describe the characterization of a panel of 102 cell lines from metastatic melanomas (the NZM lines), including using whole-exome and RNA sequencing to analyse genetic variants and gene expression changes in a subset of this panel. Lines possessing all major melanoma genotypes were identified, and hierarchical clustering of gene expression profiles revealed four broad subgroups of cell lines. Immunogenotyping identified a range of HLA haplotypes as well as expression of neoantigens and cancer-testis antigens in the lines. Together, these characteristics make the NZM panel a valuable resource for cell-based, immunological and xenograft studies to better understand the diversity of melanoma biology and the responses of melanoma to therapeutic interventions.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Biomarcadores Tumorais / Regulação Neoplásica da Expressão Gênica / Genômica / Exoma / Melanoma / Modelos Biológicos / Mutação Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Biomarcadores Tumorais / Regulação Neoplásica da Expressão Gênica / Genômica / Exoma / Melanoma / Modelos Biológicos / Mutação Idioma: En Ano de publicação: 2021 Tipo de documento: Article