Authors
Furney, STurajlic, S
Fenwick, K
Lambros, M
Mackay, A
Ricken, G
Mitsopoulos, C
Kozarewa, I
Hakas, J
Zvelebil, M
Lord, C
Ashworth, A
Reis-Filho, J
Herlyn, M
Murata, H
Marais, Richard
Affiliation
Signal Transduction Team, Division of Cancer Biology, Institute of Cancer Research, London, UKIssue Date
2012-07
Metadata
Show full item recordAbstract
Acral melanoma is a rare melanoma subtype with distinct epidemiological, clinical and genetic features. To determine if acral melanoma cell lines are representative of this melanoma subtype, six lines were analysed by whole-exome sequencing and array comparative genomic hybridisation. We demonstrate that the cell lines display a mutation rate that is comparable to that of published primary and metastatic acral melanomas and observe a mutational signature suggestive of UV-induced mutagenesis in two of the cell lines. Mutations were identified in oncogenes and tumour suppressors previously linked to melanoma including BRAF, NRAS, KIT, PTEN and TP53, in cancer genes not previously linked to melanoma and in genes linked to DNA repair such as BRCA1 and BRCA2. Our findings provide strong circumstantial evidence to suggest that acral melanoma cell lines and acral tumours share genetic features in common and that these cells are therefore valuable tools to investigate the biology of this aggressive melanoma subtype. Data are available at: http://rock.icr.ac.uk/collaborations/Furney_et_al_2012/.Citation
Genomic characterisation of acral melanoma cell lines. 2012, 25 (4):488-92 Pigment Cell Melanoma ResJournal
Pigment Cell & Melanoma ResearchDOI
10.1111/j.1755-148X.2012.01016.xPubMed ID
22578220Type
ArticleLanguage
enISSN
1755-148Xae974a485f413a2113503eed53cd6c53
10.1111/j.1755-148X.2012.01016.x
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