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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...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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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. |
format | Online Article Text |
id | pubmed-5173039 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
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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