Association between TP53 Arg72Pro polymorphism and leukemia risk: a meta-analysis of 14 case-control studies

被引:19
作者
Tian, Xin [1 ]
Dai, Shundong [2 ,3 ,4 ]
Sun, Jing [5 ]
Jiang, Shenyi [6 ]
Jiang, Youhong [1 ]
机构
[1] China Med Univ, Affiliated Hosp 1, Canc Res Inst, Mol Oncol Lab, Shenyang 110001, Peoples R China
[2] China Med Univ, Affiliated Hosp 1, Dept Pathol, Shenyang 110001, Peoples R China
[3] China Med Univ, Coll Basic Med Sci, Shenyang 110001, Peoples R China
[4] Inst Pathol & Pathophysiol, Shenyang 110001, Peoples R China
[5] Liaoning Canc Hosp & Inst, Dept Immunol & Biotherapy, Shenyang 110042, Peoples R China
[6] China Med Univ, Affiliated Hosp 1, Dept Rheumatol, Shenyang 110001, Peoples R China
基金
中国国家自然科学基金;
关键词
ACUTE LYMPHOBLASTIC-LEUKEMIA; RING-FINGER DOMAIN; MDM2; SNP309; CODON-72; POLYMORPHISM; GENETIC-VARIATIONS; P53; VARIANTS; BIAS;
D O I
10.1038/srep24097
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The relationship between the TP53 Arg72Pro polymorphism (rs1042522) and the risk of leukemia remains controversial. Consequently, we performed a meta-analysis to accurately evaluate the association between TP53 Arg72Pro polymorphism and leukemia risk. A comprehensive search was conducted to find all eligible studies of TP53 Arg72Pro polymorphism and leukemia risk. Fourteen casecontrol studies, with 2,506 cases and 4,386 controls, were selected for analysis. The overall data failed to indicate a significant association between TP53 Arg72Pro polymorphism and the risk of leukemia (C vs. G: OR = 1.09, 95% CI = 0.93-1.26; CC vs. GC + GG: OR = 1.23, 95% CI = 0.96-1.57). In a subgroup analysis of clinical types, an increased risk was observed in the acute lymphocytic leukemia (ALL) subgroup (CC vs. GC + GG: OR = 1.73; 95% CI = 1.07-2.81) but not in the acute myeloid leukemia (AML) subgroup. In the subgroup analysis, no significant associations with ethnicity and the source of the controls were observed. In conclusion, the results suggest that there is no association between TP53 Arg72Pro polymorphism and the risk of leukemia, but the CC genotype may increase the risk of ALL TP53 Arg72Pro polymorphism CC genotype may increase the risk of ALL but is not associated with AML. Further large-scale, well-designed studies are needed to confirm our results.
引用
收藏
页数:6
相关论文
共 36 条
[1]  
Bergamaschi G, 2004, HAEMATOLOGICA, V89, P868
[2]   An intact HDM2 RING-finger domain is required for nuclear exclusion of p53 [J].
Boyd, SD ;
Tsai, KY ;
Jacks, T .
NATURE CELL BIOLOGY, 2000, 2 (09) :563-568
[3]   High order interactions of xenobiotic metabolizing genes and P53 codon 72 polymorphisms in acute leukemia [J].
Chauhan, Pradeep Singh ;
Ihsan, Rakhshan ;
Mishra, Ashwani Kumar ;
Yadav, Dhirendra Singh ;
Saluja, Sumita ;
Mittal, Vishakha ;
Saxena, Sunita ;
Kapur, Sujala .
ENVIRONMENTAL AND MOLECULAR MUTAGENESIS, 2012, 53 (08) :619-630
[4]   Association of Glutathione S-Transferase, EPHX, and p53 codon 72 Gene Polymorphisms with Adult Acute Myeloid Leukemia [J].
Chauhan, Pradeep Singh ;
Ihsan, Rakhshan ;
Yadav, Dhirendra Singh ;
Mishra, Ashwani Kumar ;
Bhushan, Bharat ;
Soni, Abha ;
Kaushal, Mishi ;
Devi, Thoudam Regina ;
Saluja, Sumita ;
Gupta, Dipendra Kumar ;
Mittal, Vishakha ;
Saxena, Sunita ;
Kapur, Sujala .
DNA AND CELL BIOLOGY, 2011, 30 (01) :39-46
[5]   Genetic Variations in MDM2 and P53 Genes Confer Risk for Adult Acute Lymphoblastic Leukemia in a Chinese Population [J].
Chen, Jialu ;
Zhu, Bo ;
Chen, Jingwei ;
Li, Yongjian .
DNA AND CELL BIOLOGY, 2013, 32 (07) :414-419
[6]   METAANALYSIS IN CLINICAL-TRIALS [J].
DERSIMONIAN, R ;
LAIRD, N .
CONTROLLED CLINICAL TRIALS, 1986, 7 (03) :177-188
[7]   A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia [J].
Di Bernardo, Maria Chiara ;
Crowther-Swanepoel, Dalemari ;
Broderick, Peter ;
Webb, Emily ;
Sellick, Gabrielle ;
Wild, Ruth ;
Sullivan, Kate ;
Vijayakrishnan, Jayaram ;
Wang, Yufei ;
Pittman, Alan M. ;
Sunter, Nicola J. ;
Hall, Andrew G. ;
Dyer, Martin J. S. ;
Matutes, Estella ;
Dearden, Claire ;
Mainou-Fowler, Tryfonia ;
Jackson, Graham H. ;
Summerfield, Geoffrey ;
Harris, Robert J. ;
Pettitt, Andrew R. ;
Hillmen, Peter ;
Allsup, David J. ;
Bailey, James R. ;
Pratt, Guy ;
Pepper, Chris ;
Fegan, Chris ;
Allan, James M. ;
Catovsky, Daniel ;
Houlston, Richard S. .
NATURE GENETICS, 2008, 40 (10) :1204-1210
[8]   TP53 R72P and MDM2 SNP309 polymorphisms in modification of childhood acute lymphoblastic leukemia susceptibility [J].
Do, Thuy N. ;
Ucisik-Akkaya, Esma ;
Davis, Charronne F. ;
Morrison, Brittany A. ;
Dorak, M. Tevfik .
CANCER GENETICS AND CYTOGENETICS, 2009, 195 (01) :31-36
[9]   MICE DEFICIENT FOR P53 ARE DEVELOPMENTALLY NORMAL BUT SUSCEPTIBLE TO SPONTANEOUS TUMORS [J].
DONEHOWER, LA ;
HARVEY, M ;
SLAGLE, BL ;
MCARTHUR, MJ ;
MONTGOMERY, CA ;
BUTEL, JS ;
BRADLEY, A .
NATURE, 1992, 356 (6366) :215-221
[10]   Examination of gender effect in birth weight and miscarriage associations with childhood cancer (United Kingdom) [J].
Dorak, M. Tevfik ;
Pearce, Mark S. ;
Hammal, Donna M. ;
McNally, Richard J. Q. ;
Parker, Louise .
CANCER CAUSES & CONTROL, 2007, 18 (02) :219-228