Prostate tumor DNA methylation is associated with cigarette smoking and adverse prostate cancer outcomes. Issue 14 (3rd May 2016)

• Record Type: Journal Article
• Authors: Shui, Irene M.; Wong, Chao‐Jen; Zhao, Shanshan; Kolb, Suzanne; Ebot, Ericka M.; Geybels, Milan S.; Rubicz, Rohina; Wright, Jonathan L.; Lin, Daniel W.; Klotzle, Brandy; Bibikova, Marina; Fan, Jian‐Bing; Ostrander, Elaine A.; Feng, Ziding; Stanford, Janet L.
• Is Part Of: Cancer. Volume 122:Issue 14(2016)
• Page Start: 2168
• Page End: 2177
• Publication Date: 2016-05-03
• Subjects: DNA methylation -- epigenetics -- prostate cancer -- prostate cancer outcomes -- smoking; Cancer -- Periodicals; Cancer -- Cytopathology -- Periodicals; 616.99405
• DOI: 10.1002/cncr.30045
• Languages: English
• ISSNs: 0008-543X

Abstract

Abstract : BACKGROUND: DNA methylation has been hypothesized as a mechanism for explaining the association between smoking and adverse prostate cancer (PCa) outcomes. This study was aimed at assessing whether smoking is associated with prostate tumor DNA methylation and whether these alterations may explain in part the association of smoking with PCa recurrence and mortality. METHODS: A total of 523 men had radical prostatectomy as their primary treatment, detailed smoking history data, long‐term follow‐up for PCa outcomes, and tumor tissue profiled for DNA methylation. Ninety percent of the men also had matched tumor gene expression data. A methylome‐wide analysis was conducted to identify differentially methylated regions (DMRs) by smoking status. To select potential functionally relevant DMRs, their correlation with the messenger RNA (mRNA) expression of corresponding genes was evaluated. Finally, a smoking‐related methylation score based on the top‐ranked DMRs was created to assess its association with PCa outcomes. RESULTS: Forty DMRs were associated with smoking status, and 10 of these were strongly correlated with mRNA expression (aldehyde oxidase 1 [ AOX1 ], claudin 5 [ CLDN5 ], early B‐cell factor 1 [ EBF1 ], homeobox A7 [ HOXA7 ], lectin galactoside‐binding soluble 3 [ LGALS3 ], microtubule‐associated protein τ [ MAPT ], protocadherin γ A [ PCDHGA ]/protocadherin γ B [ PCDHGB ], paraoxonase 3 [ PON3 ], synaptonemal complex protein 2 like [ SYCP2L ], and zinc finger and SCAN domain containing 12 [ ZSCAN12 ]). Men who were in the highest tertile for the smoking‐methylation score derived from these DMRs had a higher risk of recurrence (odds ratio [OR], 2.29; 95% confidence interval [CI], 1.42‐3.72) and lethal disease (OR, 4.21; 95% CI, 1.65‐11.78) in comparison with men in the lower 2 tertiles. CONCLUSIONS: This integrative molecular epidemiology study supports the hypothesis that smoking‐associated tumor DNA methylation changes may explain at least part of the association between smoking and adverse PCa outcomes. Future studies are warranted to confirm these findings and understand the implications for improving patient outcomes. Cancer 2016;122:2168–77 . © 2016 American Cancer Society . Abstract : This unique analysis integrates smoking status, tumor DNA methylation, tumor gene expression, and long‐term follow‐up for prostate cancer outcomes. The results support the hypothesis that smoking‐associated tumor DNA methylation changes may explain at least part of the association between smoking and adverse prostate cancer outcomes.