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Prognostic value of CpG island hypermethylation at PTGS2, RAR-beta, EDNRB, and other gene loci in patients undergoing radical prostatectomy
被引:65
作者:
Bastian, Patrick J.
Ellinger, Joerg
Heukamp, Lukas C.
Kahl, Philip
Mueller, Stefan C.
von Ruecker, Alexander
机构:
[1] Univ Klinikum Bonn, Klin & Poliklin Urol, D-53105 Bonn, Germany
[2] Univ Klinikum Bonn, Inst Pathol, D-53105 Bonn, Germany
关键词:
CpG island;
hypermethylation;
prostate cancer;
PTGS2;
EDNRB;
RAR-beta;
PSA recurrence;
D O I:
10.1016/j.eururo.2006.08.008
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: To evaluate CpG island hypermethylation in a set of candidate genes in prostate cancer (pCA) and its relationship to clinicopathologic parameters and a nomogram predicting prostate-specific antigen (PSA) recurrence after radical prostatectomy. Materials and methods: Tissues of 78 prostate carcinomas, 32 benign prostate hyperplasias (BPHs), and prostate cell lines (LNCaP, DU145, PC3, BPH-1) were examined with MethyLight polymerase chain reaction at 13 gene loci (APC, CDC6, CTNNB1, E-Cadherin, EDNRB, FGFR2, GSTP1, NAB2, PKCmu, PTGS2, RAR-beta, RASL11A, WWOX). Results: APC, RAR-beta, PTGS2, GSTP1, EDNRB, and CTNNB1 (83%,71%,65%,33%,14%, 9%, respectively) were methylated in pCA but rarely or not methylated in BPH. NAB2 and CDC6 were hypermethylated frequently in pCA (92%, 67%, respectively) and in BPH (91%, 59%, respectively). FGFR2, WWOX, E-Cadherin, PKCmu, and RASLL1A did not display noteworthy methylation in pCA (0-1%) or in BPH. CpG island hypermethylation at APC, retinoic acid receptor beta (RAR-beta), and PTGS2 discriminated with a sensitivity of 65-83% and a specificity of 97-100% between BPH and pCA. The combination of various genes increased the diagnostic expressiveness. PTGS2 hypermethylation correlated with seminal vesicle infiltration (p = 0.047), capsular penetration (p = 0.004), and pT stage (p = 0.014). RAR-beta methylation was accompanied by a higher cumulative Gleason score (p = 0.042). The probability of PSA-freesurvival calculated with a Kattan nomogram correlated inversely with CpG island hypermethylation at EDNRB, RAR-beta, and PTGS2. All prostate cancer cell lines displayed a varying degree of demethylation after 5-aza-2'deoxycytidine treatment. Conclusions: CpG island hypermethylation at various gene loci is frequent in prostate cancer and can distinguish between neoplastic and noncancerous tissue. Furthermore, hypermethylation at PTGS2, RAR-beta, and EDNRB inversely correlated with PSA- free -survival according to a Kattan nomogram and has potential prognostic value. (c) 2006 European Association of Urology. Published by Elsevier B.V. All rights reserved.
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页码:665 / 674
页数:10
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