Literature DB >> 23984804

Agonists of luteinizing hormone-releasing hormone in prostate cancer.

Ferenc G Rick1, Norman L Block, Andrew V Schally.   

Abstract

INTRODUCTION: Androgen deprivation therapy (ADT) has been the first-line standard of care for treating patients with hormone-sensitive advanced prostate cancer (PCa) for many decades. The agonists of luteinizing hormone-releasing hormone (LHRH), also called gonadotropin-releasing hormone, are still the most frequently used form of medical ADT. AREAS COVERED: This article reviews the available data and most recent information concerning the use of LHRH agonists in advanced PCa. This article also reviews the discovery and development of LHRH agonists and summarizes the clinical evidence for their efficacy in PCa. EXPERT OPINION: The introduction and application of agonists of LHRH has modernized and improved the treatment of advanced PCa. The life-saving benefits of LHRH agonists are well established, yet underestimated. Despite their efficacy, agonists of LHRH have several disadvantages or drawbacks including disease flare. The approach to ADT has been recently further refined with the development of the LHRH antagonist degarelix. Degarelix, a highly clinically effective third-generation LHRH antagonist, is currently available in most countries for therapy of advanced PCa. This new drug offers attractive alternatives to LHRH agonists for treatment of advanced PCa. A therapy for castration-resistant PCa based on a targeted cytotoxic analog of LHRH, AEZS-108, is also emerging.

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Year:  2013        PMID: 23984804     DOI: 10.1517/14656566.2013.834328

Source DB:  PubMed          Journal:  Expert Opin Pharmacother        ISSN: 1465-6566            Impact factor:   3.889


  8 in total

Review 1.  Pharmacotherapeutic Targeting of G Protein-Coupled Receptors in Oncology: Examples of Approved Therapies and Emerging Concepts.

Authors:  Rosamaria Lappano; Marcello Maggiolini
Journal:  Drugs       Date:  2017-06       Impact factor: 9.546

2.  Preclinical efficacy of growth hormone-releasing hormone antagonists for androgen-dependent and castration-resistant human prostate cancer.

Authors:  Cale D Fahrenholtz; Ferenc G Rick; Maria I Garcia; Marta Zarandi; Ren-Zhi Cai; Norman L Block; Andrew V Schally; Kerry L Burnstein
Journal:  Proc Natl Acad Sci U S A       Date:  2014-01-06       Impact factor: 11.205

3.  Potentiating effects of GHRH analogs on the response to chemotherapy.

Authors:  Andrew V Schally; Roberto Perez; Norman L Block; Ferenc G Rick
Journal:  Cell Cycle       Date:  2015       Impact factor: 4.534

4.  New therapies for relapsed castration-resistant prostate cancer based on peptide analogs of hypothalamic hormones.

Authors:  Andrew V Schally; Norman L Block; Ferenc G Rick
Journal:  Asian J Androl       Date:  2015 Nov-Dec       Impact factor: 3.285

5.  Targeted cytotoxic analog of luteinizing hormone-releasing hormone (LHRH), AEZS-108 (AN-152), inhibits the growth of DU-145 human castration-resistant prostate cancer in vivo and in vitro through elevating p21 and ROS levels.

Authors:  Petra Popovics; Andrew V Schally; Luca Szalontay; Norman L Block; Ferenc G Rick
Journal:  Oncotarget       Date:  2014-06-30

Review 6.  Heroes in endocrinology: Nobel Prizes.

Authors:  Wouter W de Herder
Journal:  Endocr Connect       Date:  2014-07-23       Impact factor: 3.335

7.  Accuracy of serum luteinizing hormone and serum testosterone measurements to assess the efficacy of medical castration in prostate cancer patients.

Authors:  Juan Morote; Imma Comas; Roser Ferrer; Jacques Planas; Anna Celma; Lucas Regis
Journal:  J Biomed Sci       Date:  2017-10-22       Impact factor: 8.410

Review 8.  Progress in Clinical Research on Gonadotropin-Releasing Hormone Receptor Antagonists for the Treatment of Prostate Cancer.

Authors:  Yi-Fu Liu; Sheng-Qiang Fu; Yu-Chang Yan; Bin-Bin Gong; Wen-Jie Xie; Xiao-Rong Yang; Ting Sun; Ming Ma
Journal:  Drug Des Devel Ther       Date:  2021-02-16       Impact factor: 4.162

  8 in total

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