Increase sensitivity in detecting superficial, low grade bladder cancer by combination analysis of hypermethylation of E-cadherin, p16, p14, RASSF1A genes in urine

被引:51
作者
Lin, Hui-Hui [1 ,3 ]
Ke, Hung-Lung [2 ,3 ]
Huang, Shu-Pin [2 ,4 ]
Wu, Wen-Jeng [2 ,4 ]
Chen, Yu-Kuei [3 ]
Chang, Lin-Li [1 ,3 ]
机构
[1] Kaohsiung Med Univ, Dept Microbiol, Kaohsiung, Taiwan
[2] Kaohsiung Med Univ, Dept Urol, Chung Ho Mem Hosp, Kaohsiung, Taiwan
[3] Kaohsiung Med Univ, Grad Inst Med, Coll Med, Kaohsiung, Taiwan
[4] Kaohsiung Med Univ, Dept Urol, Coll Med, Kaohsiung, Taiwan
关键词
Bladder cancer; E-cadherin; Methylation; p14; RASSF1A; Urine; PROMOTER HYPERMETHYLATION; PLASMA DNA; METHYLATION; PROGRESSION; RECURRENCE; NEOPLASMS; CARCINOMA; SEDIMENTS; RISK;
D O I
10.1016/j.urolonc.2008.12.008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives: To identify a better set of DNA methylation markers to detect superficial, low grade cancer cell in urine sediment for improving cancer treatment, morbidity, and mortality. Materials and Methods: Methylation-specific PCR (MSP) assay was used to detect promoter hypermethylation in 4 genes (E-cadherin, p16, p14, and RASSF1A) to identify reliable biomarkers for bladder cancer diagnosis in primary tumor DNA and urine sediment DNA from 57 bladder cancer patients. Urine DNA was compared with 20 healthy controls. Results: Fifty-one (90%) tumor DNA and 47 urine DNA (83%) samples from bladder cancer patients revealed hypermethylation in at least I of the 4 analyzed genes, whereas all urine samples from normal controls were negative. The sensitivity of MSP assay for detecting E-cadherin, p16, p14 and RASSF1A in tumor cells in voided urine was 35%, 35%, 33%, and 65%, respectively. Diagnostic sensitivity was 75% for combining RASSF1A and p14. And 83% for RASSF1A, p14 and E-cadherin. Urine cytology, however, detect only 13 (28%) cases of cancer or suspicious cancer. For detecting superficial and invasive bladder tumor, urine cytology revealed a sensitivity of 23% (6/26) and 35% (7/20), respectively. In contrast, MSP detected hypermethylation in the urine of 80% (37/46) bladder cancer patients. Moreover, hypermethylation analysis of E-cadherin, p14 or RASSF1A genes in urine sediment DNA detected in 85% (22/26) of superficial, 85% (11/13) of low grade, 75% (15/20) of invasive and 79% (26/33) of high grade bladder cancers. Importantly, hypermethylation was detected ! in the urine DNA of 90% (18/20) superficial tumors with negative or atypia cytology. Conclusions: Hypermethylation of E-cadherin, p14 or RASSF1A in urine sediment DNA is a potential biomarker for detecting superficial, low grade cancer. Besides, hypermethylation of these 3 genes is a valuable adjunct diagnostic marker to urine cytology, which can enhance the diagnostic accuracy and follow-up treatment of bladder cancer patients. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:597 / 602
页数:6
相关论文
共 30 条
[1]   Detection of circulating tumour DNA in the blood (plasma/serum) of cancer patients [J].
Anker, P ;
Mulcahy, H ;
Chen, XQ ;
Stroun, M .
CANCER AND METASTASIS REVIEWS, 1999, 18 (01) :65-73
[2]  
[Anonymous], 2012, Molecular Cloning: A Laboratory Manual
[3]  
Battagli C, 2003, CANCER RES, V63, P8695
[4]   THE ESSENTIALS OF DNA METHYLATION [J].
BIRD, A .
CELL, 1992, 70 (01) :5-8
[5]   Promoter hypermethylation is associated with tumor location, stage, and subsequent progression in transitional cell carcinoma [J].
Catto, JWF ;
Azzouzi, AR ;
Rehman, I ;
Feeley, KM ;
Cross, SS ;
Amira, N ;
Fromont, G ;
Sibony, M ;
Cussenot, O ;
Meuth, M ;
Hamdy, FC .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (13) :2903-2910
[6]  
Chan MWY, 2002, CLIN CANCER RES, V8, P464
[7]   Genetic alterations of P16INK4A and P14ARF genes in human bladder cancer [J].
Chang, LL ;
Yeh, WT ;
Yang, SY ;
Wu, WJ ;
Huang, CH .
JOURNAL OF UROLOGY, 2003, 170 (02) :595-600
[8]  
CHEN CJ, 1985, CANCER RES, V45, P5895
[9]  
Chen XQ, 1996, NAT MED, V2, P1033
[10]  
Domínguez G, 2002, CLIN CANCER RES, V8, P980