Association of MnSOD AA Genotype with the Progression of Prostate Cancer.
Association of MnSOD AA Genotype with the Progression of Prostate Cancer.
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DOI:
10.1371/journal.pone.0131325
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发表时间:
2015
期刊:
影响因子:
3.7
通讯作者:
Haas GP
中科院分区:
文献类型:
--
作者:
Iguchi T;Wang CY;Delongchamps NB;Kato M;Tamada S;Yamasaki T;de la Roza G;Nakatani T;Haas GP
To investigate whether manganese superoxide dismutase (MnSOD) genetic polymorphism is associated with the clinical significance of prostate cancer. Prostates were obtained from 194 deceased men 45 years or older who did not have a history of prostate cancer. Serial sections and histological examinations of the prostate were performed. The MnSOD genotypes of the specimens were determined by polymerase chain reaction restriction fragment length polymorphism analysis. Of the 194 men, 31 and 26 had clinically insignificant and significant prostate cancer. Clinically significant cancer comprised 29% and 58% of the cancers in men <70 and >70 years old, respectively. The age-specific proportion of significant cancer significantly increased with the advance of age (p<0.001). MnSOD AA, as compared with the other genotypes (VA and VV together), was associated with significant prostate cancer across all ages, odds ratio (OR) 2.34, 95% confidence interval (CI) 0.99-5.49, and in men older than 69 years (OR 4.89, 95% CI 1.51-15.8), but not in men younger than 70 years. The genotype was not associated with clinically insignificant cancer regardless of age. The comparison between significant and insignificant cancer, the OR (95% CI) for MnSOD AA was 5.04 (1.05-24.2) (sensitivity 0.57, specificity 0.78, positive predictive value 0.78) in men older than 69 years. MnSOD polymorphism is strongly associated with the clinical significance of prostate cancer in men older than 69 years, but not in men younger than 70 years suggesting that oxidative stress may be involved in the progression of the disease. MnSOD may be a clinically useful marker to predict the potential of progression of prostate cancer.
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影响因子:
254.7
作者:
Siegel, Rebecca;Ma, Jiemin;Jemal, Ahmedin
通讯作者:
Jemal, Ahmedin
DOI:
10.1007/s00432-009-0742-x
发表时间:
2010-07-01
影响因子:
3.6
作者:
Mao, Chen;Qiu, Li-Xin;Chen, Qing
通讯作者:
Chen, Qing
DOI:
10.1097/00008571-200303000-00004
发表时间:
2003-03-01
期刊:
PHARMACOGENETICS
影响因子:
--
作者:
Sutton, A;Khoury, H;Degoul, F
通讯作者:
Degoul, F
DOI:
10.1093/jnci/93.23.1818
发表时间:
2001-12-05
期刊:
JOURNAL OF THE NATIONAL CANCER INSTITUTE
影响因子:
--
作者:
Wang, LI;Miller, DP;Christiani, DC
通讯作者:
Christiani, DC
影响因子:
120.7
作者:
EPSTEIN, JI;WALSH, PC;BRENDLER, CB
通讯作者:
BRENDLER, CB