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NRAS and EPHB6 mutation rates differ in metastatic melanomas of patients in the North Island versus South Island of New Zealand

Melanoma, the most aggressive skin cancer type, is responsible for 75% of skin cancer related deaths worldwide. Given that New Zealand (NZ) has the world's highest melanoma incidence, we sought to determine the frequency of mutations in NZ melanomas in recurrently mutated genes. NZ melanomas we...

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Autores principales: Jones, Angela M., Ferguson, Peter, Gardner, Jacqui, Rooker, Serena, Sutton, Tim, Ahn, Antonio, Chatterjee, Aniruddha, Bickley, Vivienne M., Sarwar, Makhdoom, Emanuel, Patrick, Kenwright, Diane, Shepherd, Peter R., Eccles, Michael R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5173039/
https://www.ncbi.nlm.nih.gov/pubmed/27191502
http://dx.doi.org/10.18632/oncotarget.9351
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author Jones, Angela M.
Ferguson, Peter
Gardner, Jacqui
Rooker, Serena
Sutton, Tim
Ahn, Antonio
Chatterjee, Aniruddha
Bickley, Vivienne M.
Sarwar, Makhdoom
Emanuel, Patrick
Kenwright, Diane
Shepherd, Peter R.
Eccles, Michael R.
author_facet Jones, Angela M.
Ferguson, Peter
Gardner, Jacqui
Rooker, Serena
Sutton, Tim
Ahn, Antonio
Chatterjee, Aniruddha
Bickley, Vivienne M.
Sarwar, Makhdoom
Emanuel, Patrick
Kenwright, Diane
Shepherd, Peter R.
Eccles, Michael R.
author_sort Jones, Angela M.
collection PubMed
description Melanoma, the most aggressive skin cancer type, is responsible for 75% of skin cancer related deaths worldwide. Given that New Zealand (NZ) has the world's highest melanoma incidence, we sought to determine the frequency of mutations in NZ melanomas in recurrently mutated genes. NZ melanomas were from localities distributed between North (35°S-42°S) and South Islands (41°S-47°S). A total of 529 melanomas were analyzed for BRAF exon 15 mutations by Sanger sequencing, and also by Sequenom MelaCarta MassARRAY. While, a relatively low incidence of BRAF(V600E) mutations (23.4%) was observed overall in NZ melanomas, the incidence of NRAS mutations in South Island melanomas was high compared to North Island melanomas (38.3% vs. 21.9%, P=0.0005), and to The Cancer Genome Atlas database (TCGA) (38.3% vs. 22%, P=0.0004). In contrast, the incidence of EPHB6(G404S) mutations was 0% in South Island melanomas, and was 7.8% in North Island (P=0.0002). Overall, these data suggest that melanomas from geographically different regions in NZ have markedly different mutation frequencies, in particular in the NRAS and EPHB6 genes, when compared to TCGA or other populations. These data have implications for the causation and treatment of malignant melanoma in NZ.
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spelling pubmed-51730392016-12-23 NRAS and EPHB6 mutation rates differ in metastatic melanomas of patients in the North Island versus South Island of New Zealand Jones, Angela M. Ferguson, Peter Gardner, Jacqui Rooker, Serena Sutton, Tim Ahn, Antonio Chatterjee, Aniruddha Bickley, Vivienne M. Sarwar, Makhdoom Emanuel, Patrick Kenwright, Diane Shepherd, Peter R. Eccles, Michael R. Oncotarget Research Paper Melanoma, the most aggressive skin cancer type, is responsible for 75% of skin cancer related deaths worldwide. Given that New Zealand (NZ) has the world's highest melanoma incidence, we sought to determine the frequency of mutations in NZ melanomas in recurrently mutated genes. NZ melanomas were from localities distributed between North (35°S-42°S) and South Islands (41°S-47°S). A total of 529 melanomas were analyzed for BRAF exon 15 mutations by Sanger sequencing, and also by Sequenom MelaCarta MassARRAY. While, a relatively low incidence of BRAF(V600E) mutations (23.4%) was observed overall in NZ melanomas, the incidence of NRAS mutations in South Island melanomas was high compared to North Island melanomas (38.3% vs. 21.9%, P=0.0005), and to The Cancer Genome Atlas database (TCGA) (38.3% vs. 22%, P=0.0004). In contrast, the incidence of EPHB6(G404S) mutations was 0% in South Island melanomas, and was 7.8% in North Island (P=0.0002). Overall, these data suggest that melanomas from geographically different regions in NZ have markedly different mutation frequencies, in particular in the NRAS and EPHB6 genes, when compared to TCGA or other populations. These data have implications for the causation and treatment of malignant melanoma in NZ. Impact Journals LLC 2016-05-13 /pmc/articles/PMC5173039/ /pubmed/27191502 http://dx.doi.org/10.18632/oncotarget.9351 Text en Copyright: © 2016 Jones et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Jones, Angela M.
Ferguson, Peter
Gardner, Jacqui
Rooker, Serena
Sutton, Tim
Ahn, Antonio
Chatterjee, Aniruddha
Bickley, Vivienne M.
Sarwar, Makhdoom
Emanuel, Patrick
Kenwright, Diane
Shepherd, Peter R.
Eccles, Michael R.
NRAS and EPHB6 mutation rates differ in metastatic melanomas of patients in the North Island versus South Island of New Zealand
title NRAS and EPHB6 mutation rates differ in metastatic melanomas of patients in the North Island versus South Island of New Zealand
title_full NRAS and EPHB6 mutation rates differ in metastatic melanomas of patients in the North Island versus South Island of New Zealand
title_fullStr NRAS and EPHB6 mutation rates differ in metastatic melanomas of patients in the North Island versus South Island of New Zealand
title_full_unstemmed NRAS and EPHB6 mutation rates differ in metastatic melanomas of patients in the North Island versus South Island of New Zealand
title_short NRAS and EPHB6 mutation rates differ in metastatic melanomas of patients in the North Island versus South Island of New Zealand
title_sort nras and ephb6 mutation rates differ in metastatic melanomas of patients in the north island versus south island of new zealand
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5173039/
https://www.ncbi.nlm.nih.gov/pubmed/27191502
http://dx.doi.org/10.18632/oncotarget.9351
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