Aberrant promoter hypermethylation of p21 (WAF1/CIP1) gene and its impact on expression and role of polymorphism in the risk of breast cancer

被引:20
作者
Askari, Marjan [1 ]
Sobti, Ranbir Chander [1 ]
Nikbakht, Mohsen [2 ]
Sharma, Suresh C. [3 ]
机构
[1] Panjab Univ, Dept Biotechnol, Chandigarh 160014, India
[2] Univ Tehran Med Sci, Hematol Oncol & Stem Cell Transplantat Res Ctr, Tehran, Iran
[3] Post Grad Inst Med Educ & Res, Dept Radiotherapy & Oncol, Chandigarh, India
关键词
p21 (Waf-1); Breast cancer; Hypermethylation; Expression; Polymorphism; P53; POLYMORPHISMS; SOLID TUMORS; G(1) ARREST; P21(WAF1/CIP1); CODON-31; ASSOCIATION; INHIBITOR; CARCINOMA; WAF1; P16(INK4A);
D O I
10.1007/s11010-013-1696-5
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
p21 (Waf-1) is a cyclin-dependent kinase inhibitor that plays essential roles in cell growth arrest, terminal differentiation, and apoptosis. Statistically significant difference in the level of methylation of p21/CIP1 (p < 0. 05) between the patients with breast cancer and the healthy controls was observed. Risk of breast cancer was increased in patients with hypermethylated p21/CIP1 promoter by 2.31-fold (OR = 2.31, 95 % CI 1.95-2.74). The downregulation of p21/CIP1 mRNA expression was statistically significant in patients with methylated promoter (p < 0.00) in comparison to patients with unmethylated genes. Downregulation of mRNA expression of p21/CIP1 was up to 79 % due to promoter hypermethylation. We examined several p21/CIP1 genotypes in the patients with breast cancer and found that there is no significant association of these p21/CIP1 genotypes with the risk of developing breast cancer. However, a significant 2.21-fold increase in the chance of developing breast cancer was observed in the candidates carrying at least one allele Arg mutant in p21/CIP1 genotype (i.e., Ser/Arg + Arg/Arg) with age > 50 (OR = 2.21; 95 % CI 1.03-4.79).
引用
收藏
页码:19 / 26
页数:8
相关论文
共 48 条
[1]   Loss of p21WAF1/CIP1 accelerates Ras oncogenesis in a transgenic/knockout mammary cancer model [J].
Adnane, J ;
Jackson, RJ ;
Nicosia, SV ;
Cantor, AB ;
Pledger, WJ ;
Sebti, SM .
ONCOGENE, 2000, 19 (47) :5338-5347
[2]  
BAE IS, 1995, CANCER RES, V55, P2387
[3]   The codon 31 polymorphism of the p53-inducible gene p21 shows distinct differences between major ethnic groups [J].
Birgander, R ;
Sjalander, A ;
Saha, N ;
Spitsyn, V ;
Beckman, L ;
Beckman, G .
HUMAN HEREDITY, 1996, 46 (03) :148-154
[4]  
Boestein D, 2003, NATURE GENET S, V3, P228
[5]  
Caffo O, 1996, CLIN CANCER RES, V2, P1591
[6]   Gene expression profiling for the prediction of therapeutic response to docetaxel in patients with breast cancer [J].
Chang, JC ;
Wooten, EC ;
Tsimelzon, A ;
Hilsenbeck, SG ;
Gutierrez, MC ;
Elledge, R ;
Mohsin, S ;
Osborne, CK ;
Chamness, GC ;
Allred, DC ;
O'Connell, P .
LANCET, 2003, 362 (9381) :362-369
[7]  
CHEDID M, 1994, ONCOGENE, V9, P3021
[8]  
CHEN YQ, 1995, CANCER RES, V55, P4536
[9]   The role of TP53 and p21 gene polymorphisms in breast cancer biology in a well specified and characterized German cohort [J].
Ebner, Florian ;
Schremmer-Danninger, Elisabeth ;
Rehbock, Joachim .
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 2010, 136 (09) :1369-1375
[10]  
ELDEIRY WS, 1994, CANCER RES, V54, P1169