作者: Carmen Jerónimo , Rui Henrique , Mohammad O. Hoque , Elizabeth Mambo , Franclim R. Ribeiro
DOI: 10.1158/1078-0432.CCR-04-0894
关键词: Cancer research 、 GSTP1 、 Adenocarcinoma 、 Prostate cancer 、 DNA methylation 、 CDKN2A 、 Biology 、 PCA3 、 Prostate 、 Methylation
摘要: Purpose: Promoter hypermethylation is an alternative pathway for gene silencing in neoplastic cells and a promising cancer detection marker. Although quantitative methylation-specific PCR (QMSP) of the GSTP1 promoter has demonstrated near perfect specificity prostate biopsies, we postulated that identification characterization additional methylation markers might further improve its high (80–90%) sensitivity. Experimental Design: We surveyed nine promoters ( , MGMT p14 / ARF p16 CDKN2A RASSF1A APC TIMP3 S100A2 CRBP1 ) by QMSP tissue DNA from 118 carcinomas, 38 paired high-grade prostatic intraepithelial neoplasias (HGPIN), 30 benign hyperplasias (BPH). The levels were calculated correlated with clinical pathologic indicators. Results: Only frequencies significantly higher carcinoma compared BPH P differed between HGPIN, and/or HGPIN or theoretical sensitivity 98.3% carcinoma, 100% specificity. Methylation found to correlate tumor grade stage ). Conclusions: Our data demonstrate existence progressive increase several cancer-related genes carcinogenesis, providing augment molecular carcinoma. Because are associated advanced stage, indicators currently used predict aggressiveness.