Effect of DNA Methylation on Identification of Aggressive Prostate Cancer

被引:45
作者
Alumkal, Josh J.
Zhang, Zhe
Humphreys, Elizabeth B.
Bennett, Christina
Mangold, Leslie A.
Carducci, Michael A.
Partin, Alan W.
Garrett-Mayer, Elizabeth
DeMarzo, Angelo M.
Herman, James G.
机构
[1] Oregon Hlth & Sci Univ, Div Hematol & Med Oncol, Portland, OR 97201 USA
[2] Johns Hopkins Med Inst, Div Oncol Biostat, Prostate Canc Program, Baltimore, MD 21231 USA
[3] Johns Hopkins Med Inst, Sidney Kimmel Comprehens Canc Ctr, Div Tumor Biol, James Buchanan Brady Urol Inst, Baltimore, MD 21231 USA
[4] Johns Hopkins Med Inst, Dept Pathol, Baltimore, MD 21231 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/j.urology.2007.12.060
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVES Biochemical (prostate-specific antigen) recurrence of prostate cancer after radical prostatectomy remains a major problem. Better biomarkers are needed to identify high-risk patients. DNA methylation of promoter regions leads to gene silencing in many cancers. In this study, we assessed the effect of DNA methylation on the identification of recurrent prostate cancer. METHODS We studied the methylation status of 15 pre-specified genes using methylation-specific polymerase chain reaction on tissue samples from 151 patients with localized prostate cancer and at least 5 years of follow-up after prostatectomy. RESULTS On multivariate logistic regression analysis, a high Gleason score and involvement of the capsule, lymph nodes, seminal vesicles, or Surgical margin were associated with an increased risk of biochemical recurrence. Methylation of CDH13 by itself (odds ratio 5.50, 95% confidence interval [CI] 1.34 to 22.67; P = 0.02) or combined with methylation of ASC (odds ratio 5.64, 95% CI 1.47 to 21.7; P = 0.01) was also associated with an increased risk of biochemical recurrence. The presence of methylation of ASC and/or CDH13 yielded a sensitivity of 72.3% (95% CI 57% to 84.4%) and necative predictive value of 79% (95% CI 66.8% to 88.3%), similar to the weighted risk of recurrence (determined from the lymph node status, seminal vesicle status, surgical margin status, and postoperative Gleason score), a powerful clinicopathologic prognostic score. However, 34% (95% CI 21% to 49%) of the patients with recurrence were identified by the methylation profile of ASC and CDH13 rather than the weighted risk of recurrence. CONCLUSIONS The results Of Our study have shown that methylation of CDH13 alone or combined with methylation of ASC is independently associated with an increased risk of biochemical recurrence after radical prostatectomy even considering the weighted risk of recurrence score. These findings should be validated in an independent, larger cohort of patients with prostate cancer who have undergone radical prostatectomy. UROLOGY 72: 1234-1239, 2008. (C) 2008 Elsevier Inc.
引用
收藏
页码:1234 / 1239
页数:6
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