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TERT promoter mutations are frequent and show association with MED12 mutations in phyllodes tumors of the breast
BACKGROUND: Phyllodes tumors are rare fibroepithelial neoplasms of the breast, which carry the potential risk of local recurrence and metastasis. Phyllodes tumors share several histological features with fibroadenomas, and no widely accepted markers for distinguishing these lesions have been identif...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4647876/ https://www.ncbi.nlm.nih.gov/pubmed/26355235 http://dx.doi.org/10.1038/bjc.2015.326 |
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author | Yoshida, Masayuki Ogawa, Reiko Yoshida, Hiroshi Maeshima, Akiko Kanai, Yae Kinoshita, Takayuki Hiraoka, Nobuyoshi Sekine, Shigeki |
author_facet | Yoshida, Masayuki Ogawa, Reiko Yoshida, Hiroshi Maeshima, Akiko Kanai, Yae Kinoshita, Takayuki Hiraoka, Nobuyoshi Sekine, Shigeki |
author_sort | Yoshida, Masayuki |
collection | PubMed |
description | BACKGROUND: Phyllodes tumors are rare fibroepithelial neoplasms of the breast, which carry the potential risk of local recurrence and metastasis. Phyllodes tumors share several histological features with fibroadenomas, and no widely accepted markers for distinguishing these lesions have been identified. METHODS: We analyzed molecular abnormalities related to telomere elongation in tumors, including TERT promoter mutations, as well as loss of expression of ATRX and DAXX, in a total of 104 phyllodes tumors and fibroadenomas. RESULTS: Sequencing analyses showed that TERT promoter mutations were frequent in phyllodes tumors (30/46, 65%), but rare in fibroadenomas (4/58, 7%). Among phyllodes tumors, the mutations were more frequent in borderline tumors (13/15, 87%), but were also common in benign (9/18, 50%) and malignant tumors (8/13, 62%). Remarkably, all but one TERT promoter-mutated tumor also contained MED12 mutations, indicating that these mutations are strongly associated (P=8.4 × 10(−6)). Expression of ATRX and DAXX, as evaluated by immunohistochemistry, was retained in all tumors. CONCLUSIONS: Our observations suggest a critical role of TERT promoter mutations, in cooperation with MED12 mutations, in the development of phyllodes tumors. Because TERT promoter mutations are rare among fibroadenomas, their detection may be of potential use in discriminating between phyllodes tumors and fibroadenomas. |
format | Online Article Text |
id | pubmed-4647876 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46478762016-10-20 TERT promoter mutations are frequent and show association with MED12 mutations in phyllodes tumors of the breast Yoshida, Masayuki Ogawa, Reiko Yoshida, Hiroshi Maeshima, Akiko Kanai, Yae Kinoshita, Takayuki Hiraoka, Nobuyoshi Sekine, Shigeki Br J Cancer Genetics & Genomics BACKGROUND: Phyllodes tumors are rare fibroepithelial neoplasms of the breast, which carry the potential risk of local recurrence and metastasis. Phyllodes tumors share several histological features with fibroadenomas, and no widely accepted markers for distinguishing these lesions have been identified. METHODS: We analyzed molecular abnormalities related to telomere elongation in tumors, including TERT promoter mutations, as well as loss of expression of ATRX and DAXX, in a total of 104 phyllodes tumors and fibroadenomas. RESULTS: Sequencing analyses showed that TERT promoter mutations were frequent in phyllodes tumors (30/46, 65%), but rare in fibroadenomas (4/58, 7%). Among phyllodes tumors, the mutations were more frequent in borderline tumors (13/15, 87%), but were also common in benign (9/18, 50%) and malignant tumors (8/13, 62%). Remarkably, all but one TERT promoter-mutated tumor also contained MED12 mutations, indicating that these mutations are strongly associated (P=8.4 × 10(−6)). Expression of ATRX and DAXX, as evaluated by immunohistochemistry, was retained in all tumors. CONCLUSIONS: Our observations suggest a critical role of TERT promoter mutations, in cooperation with MED12 mutations, in the development of phyllodes tumors. Because TERT promoter mutations are rare among fibroadenomas, their detection may be of potential use in discriminating between phyllodes tumors and fibroadenomas. Nature Publishing Group 2015-10-20 2015-09-10 /pmc/articles/PMC4647876/ /pubmed/26355235 http://dx.doi.org/10.1038/bjc.2015.326 Text en Copyright © 2015 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/4.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ |
spellingShingle | Genetics & Genomics Yoshida, Masayuki Ogawa, Reiko Yoshida, Hiroshi Maeshima, Akiko Kanai, Yae Kinoshita, Takayuki Hiraoka, Nobuyoshi Sekine, Shigeki TERT promoter mutations are frequent and show association with MED12 mutations in phyllodes tumors of the breast |
title | TERT promoter mutations are frequent and show association with MED12 mutations in phyllodes tumors of the breast |
title_full | TERT promoter mutations are frequent and show association with MED12 mutations in phyllodes tumors of the breast |
title_fullStr | TERT promoter mutations are frequent and show association with MED12 mutations in phyllodes tumors of the breast |
title_full_unstemmed | TERT promoter mutations are frequent and show association with MED12 mutations in phyllodes tumors of the breast |
title_short | TERT promoter mutations are frequent and show association with MED12 mutations in phyllodes tumors of the breast |
title_sort | tert promoter mutations are frequent and show association with med12 mutations in phyllodes tumors of the breast |
topic | Genetics & Genomics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4647876/ https://www.ncbi.nlm.nih.gov/pubmed/26355235 http://dx.doi.org/10.1038/bjc.2015.326 |
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