Volume 119, Issue 7 pp. 460-467

Genetic polymorphisms of TP53-binding protein 1 (TP53BP1) gene and association with breast cancer risk

RAKESH NAIDU

RAKESH NAIDU

School of Medicine and Health Sciences, Monash University Sunway Campus, Jalan Lagoon Selatan, Selangor Darul Ehsan

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YIP CHENG HAR

YIP CHENG HAR

Department of Surgery, Faculty of Medicine, University of Malaya, Kuala Lumpur

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NUR AISHAH MOHD TAIB

NUR AISHAH MOHD TAIB

University Malaya Medical Center, University of Malaya, Kuala Lumpur, Malaysia

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First published: 17 April 2011
Citations: 4
Rakesh Naidu, School of Medicine and Health Sciences, Monash University Sunway Campus, Jalan Lagoon Selatan, 46150 Bandar Sunway, Selangor Darul Ehsan, Malaysia. e-mail: [email protected]

Abstract

Naidu R, Har YC, Taib NAM. Genetic polymorphisms of TP53-binding protein 1 (TP53BP1) gene and association with breast cancer risk. APMIS 2011; 119: 460–67.

In the present study, we evaluated the association between the TP53BP1 Glu353Asp and T-885G polymorphisms and breast cancer risk as well as with the clinicopathological characteristics of the patients. Genotyping of these polymorphisms was performed on 387 breast cancer patients and 252 normal and healthy women who had no history of any malignancy using PCR-RFLP method in a hospital-based Malaysian population. Breast cancer risk was not observed among women who were heterozygous (ORadj = 0.887; 95% CI, 0.632–1.245) or homozygous (ORadj = 1.083; 95% CI, 0.595–1.969) for Asp allele, and those carriers of Asp allele (ORadj = 0.979; 95% CI, 0.771–1.243). Similarly, women who were TG heterozygotes (ORadj = 1.181; 95% CI, 0.842–1.658) or GG homozygotes (ORadj = 1.362; 95% CI, 0.746–2.486) and carriers of G allele (ORadj = 1.147; 95% CI, 0.903–1.458) were not associated with increased risk of breast cancer. Asp allele genotype was significantly associated with ER negativity (p = 0.0015) and poorly differentiated tumours (p = 0.008), but G allele genotype was not associated with the clinicopathological characteristics. In conclusion, Glu353Asp and T-885G polymorphic variants might not have an influence on breast cancer risk, thus might not be potential candidates for cancer susceptibility. Glu353Asp variant might be associated with tumour aggressiveness as defined by its association with ER negativity and poorly differentiated tumours.

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