E-cadherin expression and PSA secretion in human prostate epithelial cells

被引:6
作者
Krill, D
Thomas, A
Wu, SP
Dhir, R
Becich, MJ
机构
[1] Univ Pittsburgh, Presbyterian Univ Hosp C920, Sch Med, Pittsburgh, PA 15261 USA
[2] Univ Pittsburgh, Sch Med, Dept Pathol, Pittsburgh, PA 15261 USA
来源
UROLOGICAL RESEARCH | 2001年 / 29卷 / 04期
关键词
PSA; E-cadherin; prostate; human; cell culture;
D O I
10.1007/s002400100188
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Prostate-specific antigen (PSA) is the most widely used marker for the diagnosis of prostate cancer and is an independent predictor of prostatic capsular invasion. A number of studies have identified E-cadherin, a cell adhesion protein, as a potential invasion suppressor which is decreased in prostate adenocarcinoma. Our goal in the present study was to evaluate E-cadherin expression in primary cultures and determine the relationship between E-cadherin expression and PSA secretion in both primary cultures and the prostate tumor cell line, LNCaP. Immunohistochemical studies and Western blot analysis confirmed greater expression of E-cadherin in normal epithelial cells than tumor-derived prostate cells. This is the first report that the incubation of normal prostate epithelial cells with E-cadherin antibody increases the amount of PSA detected in the media of normal cells as well as in LNCaP. Since E-cadherin may function as an invasion suppressor, an understanding of the decreased expression of this adhesion factor and the impact on PSA secretion may aid in understanding epithelial tumorigenesis.
引用
收藏
页码:287 / 292
页数:6
相关论文
共 36 条
[31]   V-src kinase shifts the cadherin-based cell adhesion from the strong to the weak state and beta catenin is not required for the shift [J].
Takeda, H ;
Nagafuchi, A ;
Yonemura, S ;
Tsukita, S ;
Behrens, J ;
Birchmeier, W ;
Tsukita, S .
JOURNAL OF CELL BIOLOGY, 1995, 131 (06) :1839-1847
[32]  
UMBAS R, 1994, CANCER RES, V49, P2128
[33]  
VIEMINCKX K, 1991, CELL, V66, P107
[34]   HUMAN PROSTATE-SPECIFIC ANTIGEN - STRUCTURAL AND FUNCTIONAL SIMILARITY WITH SERINE PROTEASES [J].
WATT, KWK ;
LEE, PJ ;
MTIMKULU, T ;
CHAN, WP ;
LOOR, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (10) :3166-3170
[35]  
Webber MM, 1995, CLIN CANCER RES, V1, P1089
[36]   The morphogenetic role of cadherin cell adhesion molecules in human cancer: A thematic review [J].
Yap, AS .
CANCER INVESTIGATION, 1998, 16 (04) :252-261