학술논문

Assessing Associations between the AURKA-HMMR-TPX2-TUBG1 Functional Module and Breast Cancer Risk in BRCA1/2 Mutation Carriers
Document Type
article
Author
Blanco, IgnacioKuchenbaecker, KarolineCuadras, DanielWang, XianshuBarrowdale, Danielde Garibay, Gorka RuizLibrado, PabloSánchez-Gracia, AlejandroRozas, JulioBonifaci, NúriaMcGuffog, LesleyPankratz, Vernon SIslam, AbulMateo, FrancescaBerenguer, AntoniPetit, AnnaCatalà, IsabelBrunet, JoanFeliubadaló, LidiaTornero, EvaBenítez, JavierOsorio, AnaCajal, Teresa Ramón YNevanlinna, HeliAittomäki, KristiinaArun, Banu KToland, Amanda EKarlan, Beth YWalsh, ChristineLester, JennyGreene, Mark HMai, Phuong LNussbaum, Robert LAndrulis, Irene LDomchek, Susan MNathanson, Katherine LRebbeck, Timothy RBarkardottir, Rosa BJakubowska, AnnaLubinski, JanDurda, KatarzynaJaworska-Bieniek, KatarzynaClaes, KathleenVan Maerken, TomDíez, OrlandHansen, Thomas VJønson, LarsGerdes, Anne-MarieEjlertsen, Bentde la Hoya, MiguelCaldés, TrinidadDunning, Alison MOliver, ClareFineberg, ElenaCook, MargaretPeock, SusanMcCann, EmmaMurray, AlexJacobs, ChrisPichert, GabriellaLalloo, FionaChu, CarolDorkins, HuwPaterson, JoanOng, Kai-RenTeixeira, Manuel RHogervorst, Frans BLvan der Hout, Annemarie HSeynaeve, Carolinevan der Luijt, Rob BLigtenberg, Marjolijn JLDevilee, PeterWijnen, Juul TRookus, Matti AMeijers-Heijboer, Hanne EJBlok, Marinus Jvan den Ouweland, Ans MWAalfs, Cora MRodriguez, Gustavo CPhillips, Kelly-Anne APiedmonte, MarionNerenstone, Stacy RBae-Jump, Victoria LO'Malley, David MRatner, Elena SSchmutzler, Rita KWappenschmidt, BarbaraRhiem, KerstinEngel, ChristophMeindl, AlfonsDitsch, NinaArnold, NorbertPlendl, Hansjoerg JNiederacher, DieterSutter, ChristianWang-Gohrke, ShanSteinemann, DorisPreisler-Adams, SabineKast, KarinVaron-Mateeva, Raymonda
Source
PLOS ONE. 10(4)
Subject
Biological Sciences
Biomedical and Clinical Sciences
Genetics
Health Services and Systems
Health Sciences
Oncology and Carcinogenesis
Cancer
Breast Cancer
Prevention
2.1 Biological and endogenous factors
Aetiology
Aurora Kinase A
Breast Neoplasms
Carcinogenesis
Cell Cycle Proteins
Estrogen Receptor alpha
Evolution
Molecular
Extracellular Matrix Proteins
Female
Genes
BRCA1
Genes
BRCA2
Genetic Loci
Genetic Predisposition to Disease
Humans
Hyaluronan Receptors
Likelihood Functions
Mammary Glands
Human
Microtubule-Associated Proteins
Mutation
Nuclear Proteins
Polymorphism
Single Nucleotide
Retrospective Studies
Tubulin
Teixeira
BCFR
SWE-BRCA
kConFab Investigators
GEMO
General Science & Technology
Language
Abstract
While interplay between BRCA1 and AURKA-RHAMM-TPX2-TUBG1 regulates mammary epithelial polarization, common genetic variation in HMMR (gene product RHAMM) may be associated with risk of breast cancer in BRCA1 mutation carriers. Following on these observations, we further assessed the link between the AURKA-HMMR-TPX2-TUBG1 functional module and risk of breast cancer in BRCA1 or BRCA2 mutation carriers. Forty-one single nucleotide polymorphisms (SNPs) were genotyped in 15,252 BRCA1 and 8,211 BRCA2 mutation carriers and subsequently analyzed using a retrospective likelihood approach. The association of HMMR rs299290 with breast cancer risk in BRCA1 mutation carriers was confirmed: per-allele hazard ratio (HR) = 1.10, 95% confidence interval (CI) 1.04-1.15, p = 1.9 x 10(-4) (false discovery rate (FDR)-adjusted p = 0.043). Variation in CSTF1, located next to AURKA, was also found to be associated with breast cancer risk in BRCA2 mutation carriers: rs2426618 per-allele HR = 1.10, 95% CI 1.03-1.16, p = 0.005 (FDR-adjusted p = 0.045). Assessment of pairwise interactions provided suggestions (FDR-adjusted pinteraction values > 0.05) for deviations from the multiplicative model for rs299290 and CSTF1 rs6064391, and rs299290 and TUBG1 rs11649877 in both BRCA1 and BRCA2 mutation carriers. Following these suggestions, the expression of HMMR and AURKA or TUBG1 in sporadic breast tumors was found to potentially interact, influencing patients' survival. Together, the results of this study support the hypothesis of a causative link between altered function of AURKA-HMMR-TPX2-TUBG1 and breast carcinogenesis in BRCA1/2 mutation carriers.