Expression of protein C inhibitor (PCI) in benign and malignant prostatic tissues

被引:32
作者
Cao, Y
Becker, C
Lundwall, Å
Christensson, A
Gadaleanu, V
Lilja, H
Bjartell, A [1 ]
机构
[1] Lund Univ, Malmo Univ Hosp, Dept Urol, SE-20502 Malmo, Sweden
[2] Lund Univ, Malmo Univ Hosp, Dept Clin Chem, SE-20502 Malmo, Sweden
[3] Lund Univ, Malmo Univ Hosp, Dept Nephrol & Transplantat, SE-20502 Malmo, Sweden
[4] Lund Univ, Malmo Univ Hosp, Dept Pathol, SE-20502 Malmo, Sweden
[5] Mem Sloan Kettering Canc Ctr, Dept Clin Labs Urol & Med, New York, NY 10021 USA
关键词
serpin; prostate-specific antigen; prostate cancer; human glandular kallikrein-2; tissue microarray; cell lines;
D O I
10.1002/pros.10296
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND. Protein C inhibitor (PCI) occurs at high concentration in seminal plasma, and inhibits human glandular kallikrein-2 and, less readily, prostate-specific antigen. Previous studies have localized PCI in the male genital tract. Here we have performed a detailed investigation of PCI expression in the prostatic tissues, metastases, and cell lines. METHODS. Immunohistochemistry, in situ hybridization, and Western blotting were used to study prostatic tissues, metastases, and PC-3, DU-145, and LNCaP cells. RESULTS. PCI was immunolocalized in tissue microarray spots with BPH epithelium (detection rate 100%), PIN lesions (100%), tumors (96%), metastases (88%), and in all cell lines. ISH and WB supported the findings. CONCLUSIONS. PCI is widely expressed in benign prostatic epithelium, and may act as a local regulator of enzymatic activity in seminal fluid, of importance for normal sperm function. Lack of PCI expression in a subpopulation of high-grade tumor cells in combination with maintained protease expression may facilitate invasive growth patterns. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:196 / 204
页数:9
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