Inhibition of mitogenic signaling and induction of apoptosis in human bladder smooth muscle cells treated with doxazosin

被引:11
作者
Austin, PF
Cook, BL
Niederhoff, RA
Manson, SR
Coplen, DE
Weintraub, SJ
机构
[1] Washington Univ, Sch Med, Div Urol, St Louis, MO USA
[2] Washington Univ, Sch Med, Dept Cell Biol & Physiol, St Louis, MO 63110 USA
关键词
bladder; adrenergic alpha-antagonists; cell division; apoptosis;
D O I
10.1097/01.ju.0000138524.18870.af
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 [临床医学]; 100201 [内科学];
摘要
Purpose: The alpha1 antagonist doxazosin is used to treat lower urinary tract symptoms and is believed to function primarily as a smooth muscle relaxant. However, doxazosin has been shown to inhibit proliferation and induce apoptosis in nonbladder smooth muscle. Consequently, we examined the effects of doxazosin on human bladder smooth muscle cell (SMC) proliferation and apoptosis. Materials and Methods: Primary human bladder SMCs were cultured in M199 with 10% fetal bovine serum (FBS) until they reached 65% confluency and then they were made quiescent by serum starvation in M199 with 0.4% FBS for 24 hours. The quiescent bladder SMCs were pretreated for 30 minutes with doxazosin or vehicle (dimethyl sulfoxide) and then stimulated with 10% FBS for 24 hours. Measurement of 5'-bromo-2'-deoxyuridine (BrdU) uptake by flow cytometry was used to determine the effect of doxazosin on cell cycle progression. Western immunoblot was used to examine cell cycle protein expression and phosphorylation of the retinoblastoma protein (Rb) and cyclin A, both of which regulate cell cycle progression. Results: Cellular proliferation was inhibited in a dose dependent manner by doxazosin. There was nearly a 50% decrease in BrdU uptake at 10 muM doxazosin and an approximately 90% decrease in BrdU at 25 muM doxazosin. Notably, doxazosin inhibited phosphorylation of Rb and expression of cyclin A, both of which are necessary for cell cycle progression. At concentrations of 25 muM doxazosin or greater apoptosis was induced in the bladder SMCs, as indicated by an increase in subG1 DNA content. Conclusions: Our study demonstrates that doxazosin inhibits mitogen induced proliferation of human bladder SMC by blocking cell cycle progression at the of G1/S border. Doxazosin induced cell cycle inhibition appears to be at least in part due to an inhibition of mitogen induced Rb phosphorylation and cyclin A expression. At higher concentrations doxazosin induces apoptosis in human bladder SMCs.
引用
收藏
页码:1662 / 1665
页数:4
相关论文
共 20 条
[1]
Novel E2F decoy oligodeoxynucleotides inhibit in vitro vascular smooth muscle cell proliferation and in vivo neointimal hyperplasia [J].
Ahn, JD ;
Morishita, R ;
Kaneda, Y ;
Kim, HS ;
Chang, YC ;
Lee, KU ;
Park, JY ;
Lee, HW ;
Kim, YH ;
Lee, IK .
GENE THERAPY, 2002, 9 (24) :1682-1692
[2]
Review -: Induction of prostate apoptosis by α1-adrenoceptor antagonists:: mechanistic significance of the quinazoline component [J].
Anglin, IE ;
Glassman, DT ;
Kyprianou, N .
PROSTATE CANCER AND PROSTATIC DISEASES, 2002, 5 (02) :88-95
[3]
Lipopolysaccharide and inflammatory cytokines cause an inducible nitric oxide synthase-dependent bladder smooth muscle fibrotic response [J].
Austin, PF ;
Casale, AJ ;
Cain, MP ;
Rink, RC ;
Weintraub, SJ .
JOURNAL OF UROLOGY, 2003, 170 (02) :645-648
[4]
α1-adrenoceptor antagonists terazosin and doxazosin induce prostate apoptosis without affecting cell proliferation in patients with benign prostatic hyperplasia [J].
Chon, JK ;
Borkowski, A ;
Partin, AW ;
Isaacs, JT ;
Jacobs, SC ;
Kyprianou, N .
JOURNAL OF UROLOGY, 1999, 161 (06) :2002-2008
[5]
The genetics of the E2F family of transcription factors: shared functions and unique roles [J].
DeGregori, J .
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 2002, 1602 (02) :131-150
[6]
Doxazosin induces apoptosis in cardiomyocytes cultured in vitro by a mechanism that is independent of α1-adrenergic blockade [J].
González-Juanatey, JR ;
Iglesias, MJ ;
Alcaide, C ;
Piñeiro, R ;
Lago, F .
CIRCULATION, 2003, 107 (01) :127-131
[7]
Cytometric analyses to distinguish death processes [J].
Gorczyca, W .
ENDOCRINE-RELATED CANCER, 1999, 6 (01) :17-19
[8]
Doxazosin inhibits proliferation and migration of human vascular smooth-muscle cells independent of α1-adrenergic receptor antagonism [J].
Hu, ZW ;
Shi, XY ;
Hoffman, BB .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1998, 31 (06) :833-839
[9]
Hu ZW, 1999, J PHARMACOL EXP THER, V290, P28
[10]
Doxazosin inhibits retinoblastoma protein phosphorylation and G1→S transition in human coronary smooth muscle cells [J].
Kintscher, U ;
Wakino, S ;
Kim, S ;
Jackson, SM ;
Fleck, E ;
Hsueh, WA ;
Law, RE .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2000, 20 (05) :1216-1224