Evidence for a link between TNFRSF11A and risk of breast cancer

Núria Bonifaci, Marta Palafox, Pasquale Pellegrini, Ana Osorio, Javier Benítez, Paolo Peterlongo, Siranoush Manoukian, Bernard Peissel, Daniela Zaffaroni, Gaia Roversi, Monica Barile, Alessandra Viel, Frederique Mariette, Loris Bernard, Paolo Radice, Bella Kaufman, Yael Laitman, Roni Milgrom, Eitan Friedman, María E. SáezFina Climent, María Teresa Soler, Orland Diez, Judith Balmaña, Adriana Lasa, Teresa Ramón Y Cajal, María Dolores Miramar, Miguel De La Hoya, Pedro Pérez-Segura, Trinidad Caldés, Víctor Moreno, Ander Urruticoechea, Joan Brunet, Conxi Lázaro, Ignacio Blanco, Miguel Angel Pujana, Eva González-Suárez

Research output: Contribution to journalArticle

Abstract

Intracellular signaling mediated by the receptor activator of nuclear factor-κB [Rank, encoded by the tumor necrosis factor receptor superfamily, member 11a (Tnfrsf11a) gene] is fundamental for mammary gland development in mice, regulating the expansion of stem and progenitor cell compartments. Conversely, Rank overexpression in mice promotes abnormal proliferation and impairs differentiation, leading to an increased incidence of tumorigenesis. Here, we show that a common genetic variant near the 5′-end of TNFRSF11A, rs7226991, is associated with breast cancer risk in the general population and among carriers of mutations in the breast cancer 2, early onset (BRCA2) gene. Akin to the results of the Cancer and Genetics Markers of Susceptibility initiative, combined analysis of rs7226991 in two Spanish case-control studies (1,365 controls and 1,323 cases in total) revealed a significant association with risk: odds ratio (OR) = 0.88, 95% confidence interval (CI) 0.78-0.98, P trend = 0.025. Subsequent examination of BRCA1 (n = 1,017) and BRCA2 (n = 885) mutation carriers revealed a consistent association in the latter group: weighted hazard ratio (wHR) = 0.70; 95% CI 0.55-0.88; and P trend = 0.003; compared to BRCA1 mutation carriers, wHR = 0.91; 95% CI 0.76-1.10; and P trend = 0.33. The results of this study need to be replicated in other populations and with larger numbers of BRCA1/2 mutation carriers.

Original languageEnglish
Pages (from-to)947-954
Number of pages8
JournalBreast Cancer Research and Treatment
Volume129
Issue number3
DOIs
Publication statusPublished - Oct 2011

Keywords

  • BRCA1/2 mutation carriers
  • Breast cancer
  • RANK
  • TNFRSF11A

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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  • Cite this

    Bonifaci, N., Palafox, M., Pellegrini, P., Osorio, A., Benítez, J., Peterlongo, P., Manoukian, S., Peissel, B., Zaffaroni, D., Roversi, G., Barile, M., Viel, A., Mariette, F., Bernard, L., Radice, P., Kaufman, B., Laitman, Y., Milgrom, R., Friedman, E., ... González-Suárez, E. (2011). Evidence for a link between TNFRSF11A and risk of breast cancer. Breast Cancer Research and Treatment, 129(3), 947-954. https://doi.org/10.1007/s10549-011-1546-7