Polymorphisms in TRAIL receptor genes and risk of breast cancer in Spanish women

Article type: Research Article

Authors: Martinez-Ferrandis, José I.^{a; b} | Rodríguez-López, Raquel^c | Milne, Roger L.^c | González, Emilio^c | Cebolla, Elvira^a | Chirivella, Isabel^d | Zamora, Pilar^e | Arias, José I.^f | Palacios, Santiago^g | Cervantes, Andrés^d | Díez, Orland^b | Benitez, Javier^c | Armengod, M.-Eugenia^{a; *}

Affiliations: [a] Laboratorio de Genética Molecular, Centro de Investigación Príncipe Felipe, Valencia, Spain | [b] Departamento de Genética, Hospital Sant Pau, Barcelona, Spain | [c] Departamento de Genética Humana, Centro Nacional de Investigaciones Oncológicas, Madrid, Spain | [d] Servicio de Hematología y Oncología, Hospital Clínico Universitario, Universidad de Valencia, Valencia, Spain | [e] Departamento de Oncología, Hospital La Paz, Madrid, Spain | [f] Servicio de Cirugía, Hospital Monte Naranco, Oviedo, Spain | [g] Instituto Palacios, Madrid, Spain

Correspondence: [*] Corresponding author: M.-Eugenia Armengod, Centro de Investigación Príncipe Felipe, Avenida Autopista del Saler 16-3, Valencia, 46013 Spain. Tel.: +34 963289680; Fax: +34 963289701; E-mail: armengod@cipf.es.

Abstract: TRAIL is a potent inducer of apoptosis in malignant but not in normal cells. TRAIL binds to the proapoptotic death receptor DR4 and DR5 as well as to the decoy receptors DcR1 and DcR2. To evaluate the involvement of TRAIL receptor genes in breast cancer, we carried out a case-control study of eight selected polymorphisms in a large sample of Spanish women. Three of the eight selected SNPs (626G/C and 1322G/A in DR4 and 2699A/G in DcR2) showed some evidence of different genotype distributions in a random selection of 535 cases and 480 controls and were therefore studied in our entire sample (1008 cases and 768 controls). For the two DR4 polymorphisms, no differences in genotype or haplotype distribution were found between cases and controls. Interestingly, allele 2699G in the decoy receptor DcR2 appears associated with reduced breast cancer risk (P=0.05). Given that it is located in the 3' UTR, its effect might be related to DcR2 mRNA instability, or linkage disequilibrium with a functional variant residing in either DcR2 or neighbouring genes. A decreased efficiency of DcR2 to work as decoy receptor for TRAIL, would facilitate the apoptotic pathway in cells at risk.

Keywords: Breast cancer risk, trail receptors, apoptosis, polymorphisms

DOI: 10.3233/CBM-2007-3203

Journal: Cancer Biomarkers, vol. 3, no. 2, pp. 89-93, 2007