Literature DB >> 9352686

Alpha adrenoceptor blockade in the treatment of benign prostatic hyperplasia: past, present and future.

R S Kirby1, J L Pool.   

Abstract

The treatment of BPH by alpha blockade is built upon a sound anatomical, physiological and pharmacological rationale. The theory is borne out in clinical practice; alpha adrenoceptor antagonists have been shown in placebo-controlled studies to improve symptoms of BPH and increase urinary flow rate. In hypertensive patients, there is a clinically significant reduction in blood pressure, with little or no effect on the blood pressure of normotensive patients with BPH. The development of selective alpha-1 adrenoceptor antagonists with a gradual onset and long duration of action has improved the tolerability and makes this class of drug a valuable alternative to surgery in many cases. Further refinements in the selectivity of alpha-1 adrenoceptor antagonists may enable even better targeted alpha blockade for BPH in the future by specific antagonism of the alpha-1 A adrenoceptor, although this hypothesis has yet to be confirmed clinically.

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Year:  1997        PMID: 9352686     DOI: 10.1046/j.1464-410x.1997.00247.x

Source DB:  PubMed          Journal:  Br J Urol        ISSN: 0007-1331


  9 in total

Review 1.  Induction of apoptosis in the prostate by alpha1-adrenoceptor antagonists: a novel effect of "old" drugs.

Authors:  N Kyprianou; S C Jacobs
Journal:  Curr Urol Rep       Date:  2000-08       Impact factor: 3.092

Review 2.  Clinical significance of alpha1-adrenoceptor selectivity in the management of benign prostatic hyperplasia.

Authors:  J L Pool; R S Kirby
Journal:  Int Urol Nephrol       Date:  2001       Impact factor: 2.370

3.  Doxazosin induces apoptosis of benign and malignant prostate cells via a death receptor-mediated pathway.

Authors:  Jason B Garrison; Natasha Kyprianou
Journal:  Cancer Res       Date:  2006-01-01       Impact factor: 12.701

Review 4.  What is the pathologist saying? Interpretation of the prostate pathology report.

Authors:  Omar Hameed
Journal:  Curr Urol Rep       Date:  2009-05       Impact factor: 3.092

Review 5.  Growth factor signalling in prostatic growth: significance in tumour development and therapeutic targeting.

Authors:  Arich Ryan Reynolds; Natasha Kyprianou
Journal:  Br J Pharmacol       Date:  2006-02       Impact factor: 8.739

6.  Novel quinazoline-based compounds impair prostate tumorigenesis by targeting tumor vascularity.

Authors:  Jason B Garrison; Yeng-Jeng Shaw; Ching-Shih Chen; Natasha Kyprianou
Journal:  Cancer Res       Date:  2007-12-01       Impact factor: 12.701

Review 7.  Alpha adrenergic blockers in the treatment of benign hyperplasia of the prostate.

Authors:  V L Kumar; S Dewan
Journal:  Int Urol Nephrol       Date:  2000       Impact factor: 2.266

8.  The antihypertension drug doxazosin inhibits tumor growth and angiogenesis by decreasing VEGFR-2/Akt/mTOR signaling and VEGF and HIF-1α expression.

Authors:  Mi Sun Park; Boh-Ram Kim; Seung Myung Dong; Seung-Hoon Lee; Dae-Yong Kim; Seung Bae Rho
Journal:  Oncotarget       Date:  2014-07-15

9.  The antihypertension drug doxazosin suppresses JAK/STATs phosphorylation and enhances the effects of IFN-α/γ-induced apoptosis.

Authors:  Mi Sun Park; Boh-Ram Kim; Sokbom Kang; Dae-Yong Kim; Seung Bae Rho
Journal:  Genes Cancer       Date:  2014-11
  9 in total

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