Contribution of epigenetic alteration of BRCA1 and BRCA2 genes in breast carcinomas in Tunisian patients

被引:19
作者
Ben Gacem, R. [1 ]
Hachana, M. [1 ]
Ziadi, S. [1 ]
Amara, K. [1 ]
Ksia, F. [1 ]
Mokni, M. [1 ]
Trimeche, M. [1 ]
机构
[1] Farhat Hached Hosp, Dept Pathol, Sousse 4000, Tunisia
关键词
Breast cancer; BRCA1; BRCA2; Methylation; Tunisia; MAMMARY EPITHELIAL-CELLS; DNA-REPAIR DEFECT; SPORADIC BREAST; PROMOTER METHYLATION; OVARIAN-CANCER; CHROMOSOME; 13Q12-Q13; HEREDITARY BREAST; ESTROGEN-RECEPTOR; TUMORS; HYPERMETHYLATION;
D O I
10.1016/j.canep.2011.09.001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: The aim of this study was to evaluate the contribution of the BRCA1 and BRCA2 promoter methylation in the pathogenesis of sporadic breast cancer in Tunisian patients. Methods: Breast carcinoma tissues (n = 117) and available paired normal breast tissues (n = 65) from Tunisian women who had no family history were investigated for the methylation status of BRCA1 and BRCA2 promoters using methylation-specific PCR. Breast specimens from women without carcinoma (16 fibroadenomas and 5 mastopathies) were used as control. Results: Hypermethylation of BRCA1 and BRCA2 promoters was detected respectively in 60.7% and 69.2% of the carcinoma tissues, and in only 7.7% and 4.6% of the paired normal breast tissues. None of the fibroadenomas and mastopathies showed hypermethylation. Correlations were found between BRCA1 and BRCA2 hypermethylation and decrease in their mRNA expression (p = 0.02 and p = 0.009, respectively). Moreover, BRCA1 methylation correlates with patients age (p = 0.01) and triple negative (ER-, PR-, HER2-) tumors (p = 0.01). Patients with methylated BRCA1 and/or BRCA2 had a significant prolonged survivals compared to those with unmethylated tumors (p = 0.002). Conclusion: Our results suggest an important role of BRCA1 and BRCA2 promoter methylation in breast cancer development in the Tunisian population. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:190 / 197
页数:8
相关论文
共 63 条
[1]   Hereditary breast cancer: a review [J].
Arver, B ;
Du, Q ;
Chen, JD ;
Luo, LP ;
Lindblom, A .
SEMINARS IN CANCER BIOLOGY, 2000, 10 (04) :271-288
[2]   Functional significance of concomitant inactivation of hMLH1 and hMSH6 in tumor cells of the microsatellite mutator phenotype [J].
Baranovskaya, S ;
Soto, JL ;
Perucho, M ;
Malkhosyan, SR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (26) :15107-15112
[3]   DNA hypermethylation in tumorigenesis - epigenetics joins genetics [J].
Baylin, SB ;
Herman, JG .
TRENDS IN GENETICS, 2000, 16 (04) :168-174
[4]  
Ben Ahmed S, 2004, SANTE PUBLIQUE, V14, P231
[5]   Overexpression of BRCA2 gene in sporadic breast tumours [J].
Bièche, I ;
Noguès, C ;
Lidereau, R .
ONCOGENE, 1999, 18 (37) :5232-5238
[6]   Prognostic value of loss of heterozygosity at BRCA2 in human breast carcinoma [J].
Bieche, I ;
Nogues, C ;
Rivoilan, S ;
Khodja, A ;
Latil, A ;
Lidereau, R .
BRITISH JOURNAL OF CANCER, 1997, 76 (11) :1416-1418
[7]   Epigenetic silencing and deletion of the BRCA1 gene in sporadic breast cancer [J].
Birgisdottir, Valgerdur ;
Stefansson, Olafur A. ;
Bodvarsdottir, Sigridur K. ;
Hilmarsdottir, Holmfridur ;
Jonasson, Jon G. ;
Eyfjord, Jorunn E. .
BREAST CANCER RESEARCH, 2006, 8 (04)
[8]   Epigenetic inactivation of BRCA1 is associated with aberrant expression of CTCF and DNA methyltransferase (DNMT3B) in some sporadic breast tumours [J].
Butcher, Darci T. ;
Rodenhiser, David I. .
EUROPEAN JOURNAL OF CANCER, 2007, 43 (01) :210-219
[9]   BRCA1 methylation: a significant role in tumour development? [J].
Catteau, A ;
Morris, JR .
SEMINARS IN CANCER BIOLOGY, 2002, 12 (05) :359-371
[10]   Loss of heterozygosity at the BRCA1 locus in Tunisian women with sporadic breast cancer [J].
Charef-Hamza, S ;
Trimeche, M ;
Ziadi, S ;
Amara, K ;
Gaddas, N ;
Mokni, M ;
Sriha, B ;
Yacoubi, T ;
Korbi, S .
CANCER LETTERS, 2005, 224 (02) :185-191