Selective capture of prostatic basal cells and secretory epithelial cells for proteomic and genomic analysis

被引:13
作者
Diaz, JI
Cazares, LH
Corica, A
Semmes, OJ [1 ]
机构
[1] Eastern Virginia Med Sch, Dept Microbiol, Norfolk, VA 23501 USA
[2] Eastern Virginia Med Sch, Dept Mol Cell Biol, Norfolk, VA 23501 USA
[3] Eastern Virginia Med Sch, Dept Anat & Pathol, Norfolk, VA 23501 USA
[4] Eastern Virginia Med Sch, Virginia Prostate Ctr, Norfolk, VA 23501 USA
关键词
laser capture microdissection; prostate cancer; proteomics;
D O I
10.1016/j.urolonc.2004.04.010
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Basal cells play an undefined role in signaling the growth and differentiation of normal secretory epithelial cells in the human prostate. Because basal cells disappear during malignant transformation, we hypothesize that loss of basal cell function may have a permissive role in progression of prostate intraepithelial neoplasia into invasive carcinoma. We describe an immuno-laser capture microdissection approach to selectively capture basal cells. Using surface-enhanced laser desorption/ionization time-of-flight mass spectrometry, we identified several protein candidates selectively expressed in microdissected basal cells. We also demonstrate that the RNA derived form this technique is an excellent source for gene-array studies. Thus, we provide evidence that proteomic and microgenomic techniques can be successfully applied to investigate the expression profiles of basal and secretory cells after immuno-capture. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:329 / 336
页数:8
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