Quantitative RARβ2 hypermethylation:: A promising prostate cancer marker

被引:99
作者
Jerónimo, C
Henrique, R
Hoque, MO
Ribeiro, FR
Oliveira, J
Fonseca, D
Teixeira, MR
Lopes, C
Sidransky, D
机构
[1] Johns Hopkins Univ, Sch Med, Head & Neck Canc Res Div, Dept Otolaryngol Head & Neck Surg, Baltimore, MD 21205 USA
[2] Portuguese Oncol Inst Porto, Dept Genet, Oporto, Portugal
[3] Portuguese Oncol Inst Porto, Dept Pathol, Oporto, Portugal
[4] Portuguese Oncol Inst Porto, Dept Urol, Oporto, Portugal
[5] Portuguese Oncol Inst Porto, Dept Radiol, Oporto, Portugal
关键词
D O I
10.1158/1078-0432.CCR-03-0643
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Retinoic acid receptor beta2 (RARbeta2) is a tumor suppressor gene frequently hypermethylated in several human neoplasms. To further characterize this epigenetic alteration in prostate cancer progression, we examined tumor tissue from 118 patients with prostate carcinoma (PCa), 38 paired high-grade prostatic intraepithelial neoplasias (HGPIN), and nonneoplastic prostate tissue from 30 patients with benign prostate hyperplasia (BPH), using quantitative methylation-specific PCR. We found RARbeta2 hypermethylation in 97.5% of PCa, 94.7% of HGPIN, and 23.3% of BPH. Methylation levels were significantly higher in PCa compared with HGPIN and BPH (P < 0.00001). By establishing an empiric cutoff value, we were able to discriminate between neoplastic and non-neoplastic tissue, with 94.9% sensitivity and 100% specificity. Moreover, RARbeta2 methylation levels correlated with higher pathological stage (r = 0.30, P = 0.0009). This quantitative assay represents a novel and promising molecular marker that may augment current approaches for prostate cancer detection.
引用
收藏
页码:4010 / 4014
页数:5
相关论文
共 32 条
[1]
Molecular detection of tumor cells in bronchoalveolar lavage fluid from patients with early stage lung cancer [J].
Ahrendt, SA ;
Chow, JT ;
Xu, LH ;
Yang, SC ;
Eisenberger, CF ;
Esteller, M ;
Herman, JG ;
Wu, L ;
Decker, PA ;
Jen, J ;
Sidransky, D .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1999, 91 (04) :332-339
[2]
Prostatic intraepithelial neoplasia does not appear to raise serum prostate-specific antigen concentration [J].
Alexander, EE ;
Qian, JQ ;
Wollan, PC ;
Myers, RP ;
Bostwick, DG .
UROLOGY, 1996, 47 (05) :693-698
[3]
Cote S, 1997, ANTI-CANCER DRUG, V8, P56
[4]
Phase II study of all-trans retinoic acid administered intermittently for hormone refractory prostate cancer [J].
Culine, S ;
Kramar, A ;
Droz, JP ;
Théodore, C .
JOURNAL OF UROLOGY, 1999, 161 (01) :173-175
[5]
Pathological and molecular aspects of prostate cancer [J].
DeMarzo, AM ;
Nelson, WG ;
Isaacs, WB ;
Epstein, JI .
LANCET, 2003, 361 (9361) :955-964
[6]
EPSTEIN JI, 1995, PROSTATE BIOPSY INTE, P37
[7]
LNCaP prostatic adenocarcinoma cells derived from low and high passage numbers display divergent responses not only to androgens but also to retinoids [J].
Esquenet, M ;
Swinnen, JV ;
Heyns, W ;
Verhoeven, G .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1997, 62 (5-6) :391-399
[8]
A GENOMIC SEQUENCING PROTOCOL THAT YIELDS A POSITIVE DISPLAY OF 5-METHYLCYTOSINE RESIDUES IN INDIVIDUAL DNA STRANDS [J].
FROMMER, M ;
MCDONALD, LE ;
MILLAR, DS ;
COLLIS, CM ;
WATT, F ;
GRIGG, GW ;
MOLLOY, PL ;
PAUL, CL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (05) :1827-1831
[9]
Prediction of prognosis for prostatic adenocarcinoma by combined histological grading and clinical staging (Reprinted from J Urol, vol 111, pg 58-64, 1974) [J].
Gleason, DF ;
Mellinger, GT .
JOURNAL OF UROLOGY, 2002, 167 (02) :953-958
[10]
Cancer statistics, 2000 [J].
Greenlee, RT ;
Murray, T ;
Bolden, S ;
Wingo, PA .
CA-A CANCER JOURNAL FOR CLINICIANS, 2000, 50 (01) :7-33