Cytotoxic T lymphocyte antigen-4 promoter variants in breast cancer

被引:80
作者
Erfani, N
Razmkhah, M
Talei, AR
Pezeshki, AM
Doroudchi, M
Monabati, A
Ghaderi, A [1 ]
机构
[1] Shiraz Univ Med Sci, Dept Immunol, Shiraz, Iran
[2] Shiraz Univ Med Sci, Shiraz Inst Canc Res, Shiraz, Iran
[3] Shiraz Univ Med Sci, Dept Surg, Shiraz, Iran
[4] Shiraz Univ Med Sci, Dept Pathol, Shiraz, Iran
关键词
D O I
10.1016/j.cancergencyto.2005.07.020
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
CTLA4 is a coinhibitory molecule expressed mainly oil activated T lymphocytes. To test the putative involvement of CTLA-4 in inhibitory state of immunity to breast cancer, we genotyped 283 patients and 245 health control subjects for -1722 T/C, -1661 A/G, and -318 C/T single nucleotide polymorphisms in the promoter region of the CTLA4 gene. There were no significant differences in genotype, allele, or haplotype frequencies in all three loci between patients and healthy controls. Moreover, the incidence of the most frequent haplotype combination (TAC/TAC, T -1722, A -1661 C -318) was only slightly higher among healthy controls than patients (68.4 vs. 64.8%, P = 0.2). This haplotype combination was associated with lower stages of the disease (P = 0.0007), however, and higher estrogen receptor (ER) expression in patients (P = 0.006). Association with tumor prognostic or predictive factors was also observed with certain genotypes: the -1661 AA genotype was associated with lesser lymph node (LN) involvement (P = 0.017) and higher ER expression (P = 0.004), and the -318 CC genotype with lesser LN involvement (P = 0.007). These results suggest that CTLA4 promoter variants participate in the progression of breast cancer rather than in its initial development. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:114 / 120
页数:7
相关论文
共 41 条
[1]   CTLA-4 promoter variants in patients with Graves' disease and Hashimoto's thyroiditis [J].
Braun, J ;
Donner, H ;
Siegmund, T ;
Walfish, PG ;
Usadel, KH ;
Badenhoop, K .
TISSUE ANTIGENS, 1998, 51 (05) :563-566
[2]   COSTIMULATION OF ANTITUMOR IMMUNITY BY THE B7 COUNTERRECEPTOR FOR THE LYMPHOCYTE-T MOLECULES CD28 AND CTLA-4 [J].
CHEN, LP ;
ASHE, S ;
BRADY, WA ;
HELLSTROM, I ;
HELLSTROM, KE ;
LEDBETTER, JA ;
MCGOWAN, P ;
LINSLEY, PS .
CELL, 1992, 71 (07) :1093-1102
[3]   Co-inhibitory molecules of the B7-CD28 family in the control of T-cell immunity [J].
Chen, LP .
NATURE REVIEWS IMMUNOLOGY, 2004, 4 (05) :336-347
[4]   Engagement of cytotoxic T lymphocyte-associated antigen 4 (CTLA-4) induces transforming growth factor β (TGF-β) production by murine CD4+ T cells [J].
Chen, WJ ;
Jin, WW ;
Wahl, SM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (10) :1849-1857
[5]   An Mse I RFLP in the human CTLA4 promotor [J].
Deichmann, K ;
Heinzmann, A ;
Bruggenolte, E ;
Forster, J ;
Kuehr, J .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 225 (03) :817-818
[6]  
Di Girolamo V, 2000, J EXP CLIN CANC RES, V19, P155
[7]   CTLA4 alanine-17 confers genetic susceptibility to Graves' disease and to type 1 diabetes mellitus [J].
Donner, H ;
Rau, H ;
Walfish, PG ;
Braun, J ;
Siegmund, T ;
Finke, R ;
Herwig, J ;
Usadel, KH ;
Badenhoop, K .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1997, 82 (01) :143-146
[8]   A CTLA-4 polymorphism associated with susceptibility to systemic lupus erythematosus [J].
Fernandez-Blanco, L ;
Perez-Pampin, E ;
Gomez-Reino, JJ ;
Gonzalez, A .
ARTHRITIS AND RHEUMATISM, 2004, 50 (01) :328-329
[9]   The human PD-1 gene: complete cDNA, genomic organization, and developmentally regulated expression in B cell progenitors [J].
Finger, LR ;
Pu, JY ;
Wasserman, R ;
Vibhakar, R ;
Louie, E ;
Hardy, RR ;
Burrows, PD ;
Billips, LG .
GENE, 1997, 197 (1-2) :177-187
[10]   Cytotoxic T lymphocyte antigen-4 gene in breast cancer [J].
Ghaderi, A ;
Yeganeh, F ;
Kalantari, T ;
Talei, AR ;
Pezeshki, AM ;
Doroudchi, M ;
Dehaghani, AS .
BREAST CANCER RESEARCH AND TREATMENT, 2004, 86 (01) :1-7