Expression of Androgen and Estrogen Signaling Components and Stem Cell Markers to Predict Cancer Progression and Cancer-Specific Survival in Patients with Metastatic Prostate Cancer

被引:34
作者
Fujimura, Tetsuya [1 ]
Takahashi, Satou [2 ]
Urano, Tomohiko [3 ,4 ]
Takayama, Kenichi [3 ,4 ]
Sugihara, Toru [1 ]
Obinata, Daisuke [2 ]
Yamada, Yuta [1 ]
Kumagai, Jimpei [1 ]
Kume, Haruki [1 ]
Ouchi, Yasuyoshi [3 ]
Inoue, Satoshi [3 ,4 ]
Homma, Yukio [1 ]
机构
[1] Univ Tokyo, Grad Sch Med, Dept Urol, Tokyo 1138655, Japan
[2] Nihon Univ, Grad Sch Med, Dept Urol, Tokyo, Japan
[3] Univ Tokyo, Grad Sch Med, Dept Geriatr Med, Tokyo 1138655, Japan
[4] Univ Tokyo, Grad Sch Med, Dept Antiaging Med, Tokyo 1138655, Japan
基金
日本学术振兴会;
关键词
BREAST-CANCER; DEPRIVATION; GENE; CASTRATION; CARCINOMA; CHROMATIN; THERAPY; PROTEIN; GROWTH; RNA;
D O I
10.1158/1078-0432.CCR-13-1105
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Genes of androgen and estrogen signaling cells and stem cell-like cells play crucial roles in prostate cancer. This study aimed to predict clinical failure by identifying these prostate cancer-related genes. Experimental Design: We developed models to predict clinical failure using biopsy samples from a training set of 46 and an independent validation set of 30 patients with treatment-naive prostate cancer with bone metastasis. Cancerous and stromal tissues were separately collected by laser-captured microdissection. We analyzed the association between clinical failure andmRNAexpression of the following genes androgen receptor (AR) and its related genes (APP, FOX family, TRIM 36, Oct1, and ACSL 3), stem cell-like molecules (Klf4, c-Myc, Oct 3/4, and Sox2), estrogen receptor (ER), Her2, PSA, and CRP. Results: Logistic analyses to predict prostate-specific antigen (PSA) recurrence showed an area under the curve (AUC) of 1.0 in both sets for Sox2, Her2, and CRP expression in cancer cells, AR and ERa expression in stromal cells, and clinical parameters. We identified 10 prognostic factors for cancer-specific survival (CSS): Oct1, TRIM36, Sox2, and c-Myc expression in cancer cells; AR, Klf4, and ERa expression in stromal cells; and PSA, Gleason score, and extent of disease. Onthe basis of these factors, patients were divided into favorable-, intermediate-, and poor-risk groups according to the number of factors present. Five-year CSS rates for the 3 groups were 90%, 32%, and12% in the training set and 75%, 48%, and0% in the validation set, respectively. Conclusions: Expression levels of androgen-and estrogen signaling components and stem cell markers are powerful prognostic tools. (C) 2014 AACR.
引用
收藏
页码:4625 / 4635
页数:11
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