MICA‐129 Met/Val polymorphism could be a genetic biomarker for Familial Breast Cancer in the Tunisian population. (11th February 2020)

• Record Type: Journal Article
• Authors: Ouni, Nesrine; Ben Chaaben, Arij; Ayari, Fayza; Douik, Hayet; Guizani, Imen; Benammar‐Elgaaied, Amel; Guemira, Fethi; Tamouza, Ryad
• Is Part Of: International journal of immunogenetics. Volume 47:Number 5(2020:Oct.)
• Page Start: 406
• Page End: 413
• Publication Date: 2020-02-11
• Subjects: early‐onset breast cancer -- familial breast cancer -- MICA -- polymorphism -- Tunisian population; Immunogenetics -- Periodicals; 571.9648
• DOI: 10.1111/iji.12480
• Languages: English
• ISSNs: 1744-3121

Abstract

Abstract: Identification of candidate genes associated with susceptibility of breast cancer can have a significant impact at a cancer management national healthcare systems level, making genetic testing more affordable and cost‐effective. We have previously shown that the major histocompatibility complex class I‐related chain A (MICA) was related to breast cancer and plays an important role in modulating immune response mechanisms through NKG2D receptor activation. Compared to our previous study, in this work, we recruited a new cohort composed of 354 unrelated Tunisian women affected by breast cancer and 380 age‐matched women as controls, all genotyped for MICA‐129 Met/Val (rs 1051792). Subsequently, we exanimated the distribution of this polymorphism in ten families. As a result, an association was found between the Val allele and Val/Val genotype and the risk of breast cancer ( p = 2.5 × 10 –15 ; OR = 2.40; p = 6.5 × 10 –13 ; OR = 3.03, respectively). Stratified analysis with age and family history of cancer revealed an association between the Val/Val genotype and younger patients <40 years ( p = .003; OR = 2.03). Among those patients having a family history of cancer, 68% had a Val/Val genotype ( p = .02; OR = 1.82). In the family study, an analyse of pedigrees revealed that the majority of families showed the development of breast cancer at a young age. Moreover, all patients diagnosed with early‐onset breast cancer had a Val/Val genotype. Our results lead us to propose that this polymorphism may be an inherited genetic biomarker contributing to an increased breast cancer risk in Tunisian women.