激光捕获显微切割
显微解剖
基质
上皮
生物
前列腺
雄激素受体
实时聚合酶链反应
孕酮受体
基因表达
雌激素受体
增生
分子生物学
雌激素受体
病理
基因
内分泌学
前列腺癌
免疫组织化学
医学
遗传学
免疫学
癌症
乳腺癌
作者
Kazuhiro Suzuki,Hiroshi Matsui,Masaru Hasumi,Yoshihiro Ono,Haruki Nakazato,Hidekazu Koike,Kazuto Ito,Yoshitatsu Fukabori,Kohei Kurokawa,Hidetoshi Yamanaka
出处
期刊:PubMed
日期:2002-03-26
卷期号:21 (6A): 3861-4
被引量:13
摘要
Human benign prostatic hyperplasia (BPH) nodules consist of epithelium and stroma that have different properties functionally as well as morphologically. To investigate the molecular profiles of the prostate gland, separate examination of these components are necessary. Laser-capture microdissection (LCM) is a newly-developed device which enables one to dissect interesting parts of tissues under the microscope. In the current work we studied the gene expression profiles of prostatic epithelium and stroma using LCM. Androgen receptor (AR), estrogen receptor alpha and beta (ER alpha and ER beta), progesterone receptor (PR) and 5-alpha reductase type I and type II (5alphaR I and 5alphaR II) gene expressions were studied by RT-PCR. All of these genes were expressed both in the epithelium and stroma. Furthermore, AR transcript was quantified by quantitative real-time PCR. AR transcript ranged from 302 to 1440 copies per 10(5) GAPDH copies and from 257 to 3223 copies per 10(5) GAPDH copies in the epithelium and stroma, respectively. Thus, LCM and quantitative real-time PCR are powerful tools for molecular analysis of heterogeneous tissues including prostate gland.
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