Myc-driven murine prostate cancer shares molecular features with human prostate tumors

被引:615
作者
Ellwood-Yen, K
Graeber, TG
Wongvipat, J
Iruela-Arispe, ML
Zhang, JF
Matusik, R
Thomas, GV [1 ]
Sawyers, CL
机构
[1] Univ Calif Los Angeles, Dept Med, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Dept Urol, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Dept Mol & Med Pharmacol, Los Angeles, CA 90095 USA
[4] Univ Calif Los Angeles, Dept Pathol, Los Angeles, CA 90095 USA
[5] Univ Calif Los Angeles, DOE Inst Genom & Proteom, Los Angeles, CA 90095 USA
[6] Univ Calif Los Angeles, David Geffen Sch Med, Jonsson Comprehens Canc Ctr, Los Angeles, CA 90095 USA
[7] Univ Calif Los Angeles, Howard Hughes Med Inst, Los Angeles, CA 90095 USA
[8] Univ Calif Los Angeles, Dept Mol Cell & Dev Biol, Los Angeles, CA 90095 USA
[9] Vanderbilt Univ, Sch Med, Dept Urol, Nashville, TN 37232 USA
[10] Univ Alabama Birmingham, Dept Dermatol, Birmingham, AL 35294 USA
关键词
D O I
10.1016/S1535-6108(03)00197-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Increased Myc gene copy number is observed in human prostate cancer. To define Myc's functional role, we generated transgenic mice expressing human c-Myc in the mouse prostate. All mice developed murine prostatic intraepithelial neoplasia followed by invasive adenocarcinoma. Microarray-based expression profiling identified a Myc prostate cancer expression signature, which included the putative human tumor suppressor NXK3.1. Human prostate tumor databases revealed modules of human genes that varied in concert with the Myc prostate cancer signature. This module includes the Pim-1 kinase, a gene known to cooperate with Myc in tumorigenesis, and defines a subset of human, "Myc-like" human cancers. This approach illustrates how genomic technologies can be applied to mouse cancer models to guide evaluation of human tumor databases.
引用
收藏
页码:223 / 238
页数:16
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