An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers. Issue 1 (December 2015)
- Record Type:
- Journal Article
- Title:
- An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers. Issue 1 (December 2015)
- Main Title:
- An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers
- Authors:
- Blein, Sophie
Bardel, Claire
Danjean, Vincent
McGuffog, Lesley
Healey, Sue
Barrowdale, Daniel
Lee, Andrew
Dennis, Joe
Kuchenbaecker, Karoline
Soucy, Penny
Terry, Mary
Chung, Wendy
Goldgar, David
Buys, Saundra
Janavicius, Ramunas
Tihomirova, Laima
Tung, Nadine
Dorfling, Cecilia
van Rensburg, Elizabeth
Neuhausen, Susan
Ding, Yuan
Gerdes, Anne-Marie
Ejlertsen, Bent
Nielsen, Finn
Hansen, Thomas
Osorio, Ana
Benitez, Javier
Conejero, Raquel
Segota, Ena
Weitzel, Jeffrey
Thelander, Margo
Peterlongo, Paolo
Radice, Paolo
Pensotti, Valeria
Dolcetti, Riccardo
Bonanni, Bernardo
Peissel, Bernard
Zaffaroni, Daniela
Scuvera, Giulietta
Manoukian, Siranoush
Varesco, Liliana
Capone, Gabriele
Papi, Laura
Ottini, Laura
Yannoukakos, Drakoulis
Konstantopoulou, Irene
Garber, Judy
Hamann, Ute
Donaldson, Alan
Brady, Angela
Brewer, Carole
Foo, Claire
Evans, D
Frost, Debra
Eccles, Diana
Douglas, Fiona
Cook, Jackie
Adlard, Julian
Barwell, Julian
Walker, Lisa
Izatt, Louise
Side, Lucy
Kennedy, M
Tischkowitz, Marc
Rogers, Mark
Porteous, Mary
Morrison, Patrick
Platte, Radka
Eeles, Ros
Davidson, Rosemarie
Hodgson, Shirley
Cole, Trevor
Godwin, Andrew
Isaacs, Claudine
Claes, Kathleen
De Leeneer, Kim
Meindl, Alfons
Gehrig, Andrea
Wappenschmidt, Barbara
Sutter, Christian
Engel, Christoph
Niederacher, Dieter
Steinemann, Doris
Plendl, Hansjoerg
Kast, Karin
Rhiem, Kerstin
Ditsch, Nina
Arnold, Norbert
Varon-Mateeva, Raymonda
Schmutzler, Rita
Preisler-Adams, Sabine
Markov, Nadja
Wang-Gohrke, Shan
de Pauw, Antoine
Lefol, Cédrick
Lasset, Christine
Leroux, Dominique
Rouleau, Etienne
Damiola, Francesca
Dreyfus, Hélène
Barjhoux, Laure
Golmard, Lisa
Uhrhammer, Nancy
Bonadona, Valérie
Sornin, Valérie
Bignon, Yves-Jean
Carter, Jonathan
Van Le, Linda
Piedmonte, Marion
DiSilvestro, Paul
de la Hoya, Miguel
Caldes, Trinidad
Nevanlinna, Heli
Aittomäki, Kristiina
Jager, Agnes
van den Ouweland, Ans
Kets, Carolien
Aalfs, Cora
van Leeuwen, Flora
Hogervorst, Frans
Meijers-Heijboer, Hanne
Oosterwijk, Jan
van Roozendaal, Kees
Rookus, Matti
Devilee, Peter
van der Luijt, Rob
Olah, Edith
Diez, Orland
Teulé, Alex
Lazaro, Conxi
Blanco, Ignacio
Del Valle, Jesús
Jakubowska, Anna
Sukiennicki, Grzegorz
Gronwald, Jacek
Lubinski, Jan
Durda, Katarzyna
Jaworska-Bieniek, Katarzyna
Agnarsson, Bjarni
Maugard, Christine
Amadori, Alberto
Montagna, Marco
Teixeira, Manuel
Spurdle, Amanda
Foulkes, William
Olswold, Curtis
Lindor, Noralane
Pankratz, Vernon
Szabo, Csilla
Lincoln, Anne
Jacobs, Lauren
Corines, Marina
Robson, Mark
Vijai, Joseph
Berger, Andreas
Fink-Retter, Anneliese
Singer, Christian
Rappaport, Christine
Kaulich, Daphne
Pfeiler, Georg
Tea, Muy-Kheng
Greene, Mark
Mai, Phuong
Rennert, Gad
Imyanitov, Evgeny
Mulligan, Anna
Glendon, Gord
Andrulis, Irene
Tchatchou, Sandrine
Toland, Amanda
Pedersen, Inge
Thomassen, Mads
Kruse, Torben
Jensen, Uffe
Caligo, Maria
Friedman, Eitan
Zidan, Jamal
Laitman, Yael
Lindblom, Annika
Melin, Beatrice
Arver, Brita
Loman, Niklas
Rosenquist, Richard
Olopade, Olufunmilayo
Nussbaum, Robert
Ramus, Susan
Nathanson, Katherine
Domchek, Susan
Rebbeck, Timothy
Arun, Banu
Mitchell, Gillian
Karlan, Beth
Lester, Jenny
Orsulic, Sandra
Stoppa-Lyonnet, Dominique
Thomas, Gilles
Simard, Jacques
Couch, Fergus
Offit, Kenneth
Easton, Douglas
Chenevix-Trench, Georgia
Antoniou, Antonis
Mazoyer, Sylvie
Phelan, Catherine
Sinilnikova, Olga
Cox, David
… (more) - Abstract:
- Abstract Introduction Individuals carrying pathogenic mutations in theBRCA1 andBRCA2 genes have a high lifetime risk of breast cancer.BRCA1 andBRCA2 are involved in DNA double-strand break repair, DNA alterations that can be caused by exposure to reactive oxygen species, a main source of which are mitochondria. Mitochondrial genome variations affect electron transport chain efficiency and reactive oxygen species production. Individuals with different mitochondrial haplogroups differ in their metabolism and sensitivity to oxidative stress. Variability in mitochondrial genetic background can alter reactive oxygen species production, leading to cancer risk. In the present study, we tested the hypothesis that mitochondrial haplogroups modify breast cancer risk inBRCA1/2 mutation carriers. Methods We genotyped 22, 214 (11, 421 affected, 10, 793 unaffected) mutation carriers belonging to the Consortium of Investigators of Modifiers ofBRCA1/2 for 129 mitochondrial polymorphisms using the iCOGS array. Haplogroup inference and association detection were performed using a phylogenetic approach. ALTree was applied to explore the reference mitochondrial evolutionary tree and detect subclades enriched in affected or unaffected individuals. Results We discovered that subclade T1a1 was depleted in affectedBRCA2 mutation carriers compared with the rest of clade T (hazard ratio (HR) = 0.55; 95% confidence interval (CI), 0.34 to 0.88;P = 0.01). Compared with the most frequent haplogroup inAbstract Introduction Individuals carrying pathogenic mutations in theBRCA1 andBRCA2 genes have a high lifetime risk of breast cancer.BRCA1 andBRCA2 are involved in DNA double-strand break repair, DNA alterations that can be caused by exposure to reactive oxygen species, a main source of which are mitochondria. Mitochondrial genome variations affect electron transport chain efficiency and reactive oxygen species production. Individuals with different mitochondrial haplogroups differ in their metabolism and sensitivity to oxidative stress. Variability in mitochondrial genetic background can alter reactive oxygen species production, leading to cancer risk. In the present study, we tested the hypothesis that mitochondrial haplogroups modify breast cancer risk inBRCA1/2 mutation carriers. Methods We genotyped 22, 214 (11, 421 affected, 10, 793 unaffected) mutation carriers belonging to the Consortium of Investigators of Modifiers ofBRCA1/2 for 129 mitochondrial polymorphisms using the iCOGS array. Haplogroup inference and association detection were performed using a phylogenetic approach. ALTree was applied to explore the reference mitochondrial evolutionary tree and detect subclades enriched in affected or unaffected individuals. Results We discovered that subclade T1a1 was depleted in affectedBRCA2 mutation carriers compared with the rest of clade T (hazard ratio (HR) = 0.55; 95% confidence interval (CI), 0.34 to 0.88;P = 0.01). Compared with the most frequent haplogroup in the general population (that is, H and T clades), the T1a1 haplogroup has a HR of 0.62 (95% CI, 0.40 to 0.95;P = 0.03). We also identified three potential susceptibility loci, including G13708A/rs28359178, which has demonstrated an inverse association with familial breast cancer risk. Conclusions This study illustrates how original approaches such as the phylogeny-based method we used can empower classical molecular epidemiological studies aimed at identifying association or risk modification effects. … (more)
- Is Part Of:
- Breast cancer research. Volume 17:Issue 1(2015)
- Journal:
- Breast cancer research
- Issue:
- Volume 17:Issue 1(2015)
- Issue Display:
- Volume 17, Issue 1 (2015)
- Year:
- 2015
- Volume:
- 17
- Issue:
- 1
- Issue Sort Value:
- 2015-0017-0001-0000
- Page Start:
- 1
- Page End:
- 15
- Publication Date:
- 2015-12
- Subjects:
- Breast -- Cancer -- Periodicals
616.99449 - Journal URLs:
- https://breast-cancer-research.biomedcentral.com/ ↗
http://www.bibliothek.uni-regensburg.de/ezeit/?2041618 ↗
http://link.springer.com/ ↗
http://pubmedcentral.nih.gov/tocrender.fcgi?journal=6 ↗
http://www.biomedcentral.com/1465-5411/ ↗ - DOI:
- 10.1186/s13058-015-0567-2 ↗
- Languages:
- English
- ISSNs:
- 1465-542X
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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- British Library DSC - BLDSS-3PM
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