Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/123981
Title: Mitochondrial Dna Copy Number Variation, Leukocyte Telomere Length, And Breast Cancer Risk In The European Prospective Investigation Into Cancer And Nutrition (epic) Study
Author: Campa, Daniele
Barrdahl, Myrto
Santoro, Aurelia
Severi, Gianluca
Baglietto, Laura
Omichessan, Hanane
Tumino, Rosario
Bueno de Mesquita, H. Bas
Peeters, Petra H. M.
Weiderpass, Elisabete
Chirlaque, María Dolores
Rodríguez Barranco, Miguel
Agudo, Antonio
Gunter, Marc
Dossus, Laure
Krogh, Vittorio
Matullo, Giuseppe
Trichopoulou, Antonia
Travis, Ruth C.
Canzian, Federico
Kaaks, Rudolf
Keywords: ADN mitocondrial
Telòmer
Càncer de mama
Mitochondrial DNA
Telomere
Breast cancer
Issue Date: 17-Apr-2018
Publisher: Biomed Central Ltd
Abstract: Background: Leukocyte telomere length (LTL) and mitochondrial genome (mtDNA) copy number and deletions have been proposed as risk markers for various cancer types, including breast cancer (BC).& para;& para;Methods: To gain a more comprehensive picture on how these markers can modulate BC risk, alone or in conjunction, we performed simultaneous measurements of LTL and mtDNA copy number in up to 570 BC cases and 538 controls from the European Prospective Investigation into Cancer and Nutrition (EPIC) cohort. As a first step, we measured LTL and mtDNA copy number in 96 individuals for which a blood sample had been collected twice with an interval of 15 years.& para;& para;Results: According to the intraclass correlation (ICC), we found very good stability over the time period for both measurements, with ICCs of 0.63 for LTL and 0.60 for mtDNA copy number. In the analysis of the entire study sample, we observed that longer LTL was strongly associated with increased risk of BC (OR 2.71, 95% CI 1.58-4.65, p = 3.07 x 10(-4) for highest vs. lowest quartile; OR 3.20, 95% CI 1.57-6.55, p = 1.41 x 10(-3) as a continuous variable). We did not find any association between mtDNA copy number and BC risk; however, when considering only the functional copies, we observed an increased risk of developing estrogen receptor-positive BC (OR 2.47, 95% CI 1.05-5.80, p = 0.04 for highest vs. lowest quartile).& para;& para;Conclusions: We observed a very good correlation between the markers over a period of 15 years. We confirm a role of LTL in BC carcinogenesis and suggest an effect of mtDNA copy number on BC risk.
Note: Reproducció del document publicat a: https://doi.org/10.1186/s13058-018-0955-5
It is part of: Breast Cancer Research, 2018, Vol. 20:29
URI: http://hdl.handle.net/2445/123981
Related resource: https://doi.org/10.1186/s13058-018-0955-5
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

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