Comprehensive Genome Methylation Analysis in Bladder Cancer: Identification and Validation of Novel Methylated Genes and Application of These as Urinary Tumor Markers

被引:162
作者
Reinert, Thomas [1 ]
Modin, Charlotte [1 ]
Castano, Francisco M. [1 ]
Lamy, Philippe [1 ]
Wojdacz, Tomasz K. [4 ]
Hansen, Lise Lotte [4 ]
Wiuf, Carsten [3 ]
Borre, Michael [2 ]
Dyrskjot, Lars [1 ]
Orntoft, Torben F. [1 ]
机构
[1] Aarhus Univ Hosp, Dept Mol Med, DK-8200 Aarhus N, Denmark
[2] Aarhus Univ Hosp, Dept Urol, DK-8200 Aarhus N, Denmark
[3] Univ Aarhus, Bioinformat Res Ctr BiRC, Aarhus C, Denmark
[4] Univ Aarhus, Inst Human Genet, Aarhus C, Denmark
关键词
DNA METHYLATION; PROMOTER HYPERMETHYLATION; EPIGENETIC INACTIVATION; MULTIPLE GENES; CPG-ISLANDS; PROGRESSION; ASSOCIATION; EXPRESSION; GRADE; RISK;
D O I
10.1158/1078-0432.CCR-10-2659
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Epigenetic alterations are common and can now be addressed in a parallel fashion. We investigated the methylation in bladder cancer with respect to location in genome, consistency, variation in metachronous tumors, impact on transcripts, chromosomal location, and usefulness as urinary markers. Experimental Design: A microarray assay was utilized to analyze methylation in 56 samples. Independent validation was conducted in 63 samples by a PCR-based method and bisulfite sequencing. The methylation levels in 174 urine specimens were quantified. Transcript levels were analyzed using expression microarrays and pathways were analyzed using dedicated software. Results: Global methylation patterns were established within and outside CpG islands. We validated methylation of the eight tumor markers genes ZNF154 (P < 0.0001), HOXA9 (P < 0.0001), POU4F2 (P < 0.0001), EOMES (P = 0.0005), ACOT11 (P = 0.0001), PCDHGA12 (P = 0.0001), CA3 (P = 0.0002), and PTGDR (P = 0.0110), the candidate marker of disease progression TBX4 (P < 0.04), and other genes with stage-specific methylation. The methylation of metachronous tumors was stable and targeted to certain pathways. The correlation to expression was not stringent. Chromosome 21 showed most differential methylation (P < 0.0001) and specifically hypomethylation of keratins, which together with keratin-like proteins were epigenetically regulated. In DNA from voided urine, we detected differential methylation of ZNF154 (P < 0.0001), POU4F2 (P < 0.0001), HOXA9 (P < 0.0001), and EOMES (P < 0.0001), achieving 84% sensitivity and 96% specificity. Conclusions: We initiated a detailed mapping of the methylome in metachronous bladder cancer. Novel genes with tumor, chromosome, as well as pathway-specific differential methylation in bladder cancer were identified. The methylated genes were promising cancer markers for early detection of bladder cancer. Clin Cancer Res; 17(17); 5582-92. (C)2011 AACR.
引用
收藏
页码:5582 / 5592
页数:11
相关论文
共 49 条
  • [1] Identification of DNA hypermethylation of SOX9 in association with bladder cancer progression using CpG microarrays
    Aleman, A.
    Adrien, L.
    Lopez-Serra, L.
    Cordon-Cardo, C.
    Esteller, M.
    Belbin, T. J.
    Sanchez-Carbayo, M.
    [J]. BRITISH JOURNAL OF CANCER, 2008, 98 (02) : 466 - 473
  • [2] Identification of PMF1 Methylation in Association with Bladder Cancer Progression
    Aleman, Ainel
    Cebrian, Virginia
    Alvarez, Miguel
    Lopez, Virginia
    Orenes, Esteban
    Lopez-Serra, Lidia
    Algaba, Ferran
    Bellmunt, Joaquin
    Lopez-Beltran, Antonio
    Gonzalez-Peramato, Pilar
    Cordon-Cardo, Carlos
    Garcia, Javier
    Garcia del Muro, Javier
    Esteller, Mane
    Sanchez-Carbayo, Marta
    [J]. CLINICAL CANCER RESEARCH, 2008, 14 (24) : 8236 - 8243
  • [3] Myopodin Methylation is Associated With Clinical Outcome in Patients With T1G3 Bladder Cancer
    Alvarez-Mugica, Miguel
    Cebrian, Virginia
    Fernandez-Gomez, Jesus M.
    Fresno, Florentino
    Escaf, Safwan
    Sanchez-Carbayo, Marta
    [J]. JOURNAL OF UROLOGY, 2010, 184 (04) : 1507 - 1513
  • [4] [Anonymous], 1996, EPIGENETIC MECH GENE
  • [5] Aberrant promoter methylation of multiple genes during pathogenesis of bladder cancer
    Brait, Mariana
    Begum, Shahnaz
    Carvalho, Andre L.
    Dasgupta, Santanu
    Vettore, Andre L.
    Czemiak, Bogdan
    Caballero, Otavia L.
    Westra, William H.
    Sidransky, David
    Hoque, Mohammad Obaidul
    [J]. CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2008, 17 (10) : 2786 - 2794
  • [6] The Brn-3b POU family transcription factor represses expression of the BRCA-1 anti-oncogene in breast cancer cells
    Budhram-Mahadeo, V
    Ndisang, D
    Ward, T
    Weber, BL
    Latchman, DS
    [J]. ONCOGENE, 1999, 18 (48) : 6684 - 6691
  • [7] Brn-3b enhances the pro-apoptotic effects of p53 but not its induction of cell cycle arrest by cooperating in trans-activation of bax expression
    Budhram-Mahadeo, Vishwanie S.
    Bowen, Samantha
    Lee, Sonia
    Perez-Sanchez, Christina
    Ensor, Elizabeth
    Morris, Peter J.
    Latchman, David S.
    [J]. NUCLEIC ACIDS RESEARCH, 2006, 34 (22) : 6640 - 6652
  • [8] Gene methylation and early detection of genitourinary cancer: the road ahead
    Cairns, Paul
    [J]. NATURE REVIEWS CANCER, 2007, 7 (07) : 531 - 543
  • [9] Promoter hypermethylation is associated with tumor location, stage, and subsequent progression in transitional cell carcinoma
    Catto, JWF
    Azzouzi, AR
    Rehman, I
    Feeley, KM
    Cross, SS
    Amira, N
    Fromont, G
    Sibony, M
    Cussenot, O
    Meuth, M
    Hamdy, FC
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (13) : 2903 - 2910
  • [10] Discovery of myopodin methylation in bladder cancer
    Cebrian, V.
    Alvarez, M.
    Aleman, A.
    Palou, J.
    Bellmunt, J.
    Gonzalez-Peramato, P.
    Cordon-Cardo, C.
    Garcia, J.
    Piulats, J. M.
    Sanchez-Carbayo, M.
    [J]. JOURNAL OF PATHOLOGY, 2008, 216 (01) : 111 - 119