Association of genetic polymorphisms in the telomerase reverse transcriptase gene with prostate cancer aggressiveness

被引:15
作者
Wu, Dapeng [1 ]
Yu, Hongjie [2 ]
Sun, Jielin [3 ]
Qi, Jun [1 ]
Liu, Qiang [1 ]
Li, Ruipeng [1 ]
Zheng, Siqun Lily [3 ]
Xu, Jianfeng [2 ,4 ]
Kang, Jian [1 ]
机构
[1] Shanghai Jiao Tong Univ, Xinhua Hosp, Dept Urol, Sch Med, Shanghai 200092, Peoples R China
[2] Fudan Univ, Sch Life Sci, State Key Lab Genet Engn, Shanghai 200433, Peoples R China
[3] Wake Forest Univ, Bowman Gray Sch Med, Ctr Canc Genom, Winston Salem, NC 27157 USA
[4] Fudan Univ, Fudan Inst Urol, Huashan Hosp, Shanghai 200040, Peoples R China
基金
中国国家自然科学基金;
关键词
prostate cancer; aggressiveness; telomerase reverse transcriptase; single nucleotide polymorphism; Chinese; RISK; VARIANTS; TERT; RECURRENCE; PROGNOSIS; DISEASE; LENGTH;
D O I
10.3892/mmr.2015.3410
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Telomerase reverse transcriptase (TERT), encoded by the TERT gene, is an essential component of telomerase, essential for the maintenance of telomere DNA length, chromosomal stability and cellular immortality. The aim of the present study was to evaluate the association between common genetic variations across the TERT gene region and prostate cancer (PCa) aggressiveness in a Chinese population. A total of 12 TERT tagging single-nucleotide polymorphisms (SNPs) were genotyped on the Sequenom Mass-ARRAY iPLEX((R)) platform in a case-case study with 1,210 Chinese patients with PCa. Unconditional logistic regression was used to investigate the association of genotypes with PCa aggressiveness, Gleason grade and risk of developing early-onset PCa. It was observed that the C allele of the TERT intron 2 SNP (rs2736100) was significantly associated with reduced risk of PCa aggressiveness [odds ratio (OR)=0.81; 95% confidence interval (CI): 0.66-0.99; P=0.037]. This allele was also significantly correlated with a reduced risk of developing a tumor with a high Gleason score (>7; OR=0.83; 95% CI: 0.70-0.99; P=0.039). The T allele of the intron 4 SNP (rs10069690) was found to be significantly associated with a decreased risk for an aggressive form of PCa (OR=0.76; 95% CI: 0.59-0.97; P=0.030). In addition, the A allele of rs10078761 located at the 3 end of the TERT gene exhibited a statistically significant association with the reduced risk of developing a higher grade disease (OR=0.48; 95% CI: 0.28-0.81; P=0.006). However, no association between TERT polymorphisms and age at diagnosis was observed in the present study. The present findings demonstrated for the first time, to the best of our knowledge, that genetic variations across the TERT gene are associated with PCa aggressiveness in a Chinese Han population.
引用
收藏
页码:489 / 497
页数:9
相关论文
共 30 条
  • [1] Variation at the TERT locus and predisposition for cancer
    Baird, Duncan M.
    [J]. EXPERT REVIEWS IN MOLECULAR MEDICINE, 2010, 12
  • [2] Genetic polymorphism and prostate cancer aggressiveness: A case-only study of 1,536 GWAS and candidate SNPs in African-Americans and European-Americans
    Bensen, Jeannette T.
    Xu, Zongli
    Smith, Gary J.
    Mohler, James L.
    Fontham, Elizabeth T. H.
    Taylor, Jack A.
    [J]. PROSTATE, 2013, 73 (01) : 11 - 22
  • [3] Prostate Cancer Susceptibility Variants Confer Increased Risk of Disease Progression
    Cheng, Iona
    Plummer, Sarah J.
    Neslund-Dudas, Christine
    Klein, Eric A.
    Casey, Graham
    Rybicki, Benjamin A.
    Witte, John S.
    [J]. CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2010, 19 (09) : 2124 - 2132
  • [4] Biochemical outcome after radical prostatectomy, external beam radiation therapy, or interstitial radiation therapy for clinically localized prostate cancer
    D'Amico, AV
    Whittington, R
    Malkowicz, SB
    Schultz, D
    Blank, K
    Broderick, GA
    Tomaszewski, JE
    Renshaw, AA
    Kaplan, I
    Beard, CJ
    Wein, A
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1998, 280 (11): : 969 - 974
  • [5] Dong Jin, 2011, Nan Fang Yi Ke Da Xue Xue Bao, V31, P49
  • [6] Opinion - Telomere dysfunction and the initiation of genome instability
    Feldser, DM
    Hackett, JA
    Greider, CW
    [J]. NATURE REVIEWS CANCER, 2003, 3 (08) : 623 - 627
  • [7] Genome-wide Association Study Identifies a Genetic Variant Associated with Risk for More Aggressive Prostate Cancer
    FitzGerald, Liesel M.
    Kwon, Erika M.
    Conomos, Matthew P.
    Kolb, Suzanne
    Holt, Sarah K.
    Levine, David
    Feng, Ziding
    Ostrander, Elaine A.
    Stanford, Janet L.
    [J]. CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2011, 20 (06) : 1196 - 1203
  • [8] PREDICTION OF PROGNOSIS FOR PROSTATIC ADENOCARCINOMA BY COMBINED HISTOLOGICAL GRADING AND CLINICAL STAGING
    GLEASON, DF
    MELLINGE.GT
    [J]. JOURNAL OF UROLOGY, 1974, 111 (01) : 58 - 64
  • [9] Telomerase and cancer therapeutics
    Harley, Calvin B.
    [J]. NATURE REVIEWS CANCER, 2008, 8 (03) : 167 - 179
  • [10] Overdetection, overtreatment and costs in prostate-specific antigen screening for prostate cancer
    Heijnsdijk, E. A. M.
    der Kinderen, A.
    Wever, E. M.
    Draisma, G.
    Roobol, M. J.
    de Koning, H. J.
    [J]. BRITISH JOURNAL OF CANCER, 2009, 101 (11) : 1833 - 1838