Expression signatures that correlated with Gleason score and relapse in prostate cancer

被引:78
作者
Bibikova, Marina
Chudin, Eugene
Arsanjani, Amir
Zhou, Lixin
Garcia, Eliza Wickham
Modder, Joshua
Kostelec, Monica
Barker, David
Downs, Tracy
Fan, Jian-Bing
Wang-Rodriguez, Jessica
机构
[1] Illumina Inc, San Diego, CA 92121 USA
[2] Univ Calif San Diego, Dept Surg, Div Urol, San Diego, CA 92161 USA
[3] Univ Calif San Diego, VA San Diego Healthcare Syst, San Diego, CA 92161 USA
[4] Univ Calif San Diego, Dept Pathol, San Diego, CA 92161 USA
关键词
gene expression; DASL; prostate cancer; prognosis; relapse; FFPE; bead array; biomarker;
D O I
10.1016/j.ygeno.2007.02.005
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Predicting prognosis in prostate carcinoma remains a challenge when using clinical and pathologic criteria only. We used an array-based DASL assay to identify molecular signatures for predicting prostate cancer relapse in formalin-fixed, paraffin-embedded (FFPE) prostate cancers, through gene expression profiling of 512 prioritized genes. Of the 71 patients that we analyzed, all but 3 had no evidence of residual tumor (defined as negative surgical margins) following radical prostatectomy and no patient received adjuvant therapy following surgery. All of the 71 patients had an undetectable serum PSA following radical prostatectomy. Follow-up period was 44 +/- 15 months. Highly reproducible gene expression patterns were obtained with these samples (average R-2=0.99). We identified a panel of 11 genes that correlated positively and 5 genes that correlated negatively with Gleason grade. A gene expression score (GEX) was derived from the expression levels of the 16 genes. We assessed the prognostic value of these genes and found the GEX significantly correlated with disease relapse (p=0.007). These results suggest that the approach we used is effective for expression profiling in heterogeneous FFPE tissues for cancer diagnosis/prognosis biomarker discovery and validation. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:666 / 672
页数:7
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