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Clinicopathological significance of mitochondrial D-Loop mutations in head and neck carcinoma
Mitochondrial DNA mutations have been reported in several types of tumours, including head and neck squamous cell carcinoma (HNSCC). The noncoding region of the Displacement-Loop (D-Loop) has emerged as a mutational hotspot and we recently found that they were associated with prognosis and response...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2006
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361200/ https://www.ncbi.nlm.nih.gov/pubmed/16495928 http://dx.doi.org/10.1038/sj.bjc.6602993 |
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author | Lièvre, A Blons, H Houllier, A M Laccourreye, O Brasnu, D Beaune, P Laurent-Puig, P |
author_facet | Lièvre, A Blons, H Houllier, A M Laccourreye, O Brasnu, D Beaune, P Laurent-Puig, P |
author_sort | Lièvre, A |
collection | PubMed |
description | Mitochondrial DNA mutations have been reported in several types of tumours, including head and neck squamous cell carcinoma (HNSCC). The noncoding region of the Displacement-Loop (D-Loop) has emerged as a mutational hotspot and we recently found that they were associated with prognosis and response to 5 fluorouracil (5FU) in colon cancers. In order to evaluate the frequence of D-Loop mutations in a large series of HNSCC and establish correlations with clinicopathologic parameters, we sequenced the D-Loop of 109 HNSCC before a treatment by neoadjuvant 5FU-cisplatin-based chemotherapy and surgery. Then, we correlated these mutations with prognosis and response to chemotherapy. A D-Loop mutation was identified in 21% of the tumors, the majority of them were located in a C-tract (D310). The prevalence of D310 mutations increased significantly with the number of cytosines in the matched normal tissue sequence (P=0.02). Hypopharyngeal cancer was significantly more frequent (P=0.03) and tobacco consumption more important (P=0.01) in the group of patients with D-Loop mutation. The presence of D-Loop mutation was not associated with prognosis or with response to neoadjuvant chemotherapy. These results suggest that D-Loop mutations should be considered as a cancer biomarker that may be useful for the early detection of HNSCC in individuals at risk of this cancer. |
format | Text |
id | pubmed-2361200 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23612002009-09-10 Clinicopathological significance of mitochondrial D-Loop mutations in head and neck carcinoma Lièvre, A Blons, H Houllier, A M Laccourreye, O Brasnu, D Beaune, P Laurent-Puig, P Br J Cancer Molecular Diagnostics Mitochondrial DNA mutations have been reported in several types of tumours, including head and neck squamous cell carcinoma (HNSCC). The noncoding region of the Displacement-Loop (D-Loop) has emerged as a mutational hotspot and we recently found that they were associated with prognosis and response to 5 fluorouracil (5FU) in colon cancers. In order to evaluate the frequence of D-Loop mutations in a large series of HNSCC and establish correlations with clinicopathologic parameters, we sequenced the D-Loop of 109 HNSCC before a treatment by neoadjuvant 5FU-cisplatin-based chemotherapy and surgery. Then, we correlated these mutations with prognosis and response to chemotherapy. A D-Loop mutation was identified in 21% of the tumors, the majority of them were located in a C-tract (D310). The prevalence of D310 mutations increased significantly with the number of cytosines in the matched normal tissue sequence (P=0.02). Hypopharyngeal cancer was significantly more frequent (P=0.03) and tobacco consumption more important (P=0.01) in the group of patients with D-Loop mutation. The presence of D-Loop mutation was not associated with prognosis or with response to neoadjuvant chemotherapy. These results suggest that D-Loop mutations should be considered as a cancer biomarker that may be useful for the early detection of HNSCC in individuals at risk of this cancer. Nature Publishing Group 2006-03-13 2006-02-21 /pmc/articles/PMC2361200/ /pubmed/16495928 http://dx.doi.org/10.1038/sj.bjc.6602993 Text en Copyright © 2006 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Molecular Diagnostics Lièvre, A Blons, H Houllier, A M Laccourreye, O Brasnu, D Beaune, P Laurent-Puig, P Clinicopathological significance of mitochondrial D-Loop mutations in head and neck carcinoma |
title | Clinicopathological significance of mitochondrial D-Loop mutations in head and neck carcinoma |
title_full | Clinicopathological significance of mitochondrial D-Loop mutations in head and neck carcinoma |
title_fullStr | Clinicopathological significance of mitochondrial D-Loop mutations in head and neck carcinoma |
title_full_unstemmed | Clinicopathological significance of mitochondrial D-Loop mutations in head and neck carcinoma |
title_short | Clinicopathological significance of mitochondrial D-Loop mutations in head and neck carcinoma |
title_sort | clinicopathological significance of mitochondrial d-loop mutations in head and neck carcinoma |
topic | Molecular Diagnostics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361200/ https://www.ncbi.nlm.nih.gov/pubmed/16495928 http://dx.doi.org/10.1038/sj.bjc.6602993 |
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