MAIN MOLECULAR TARGETS FOR PROSTATE CANCER THERAPY

Androgenic pathway plays a pivotal role in the development of benign and malignant prostate tumors. Most of the prostate neoplasms are hormone-dependent at the time of diagnosis. Therapeutic interventions aimed at reducing the level of testosterone in the blood allow to stop progression of the disea...

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Main Authors: G. S. Krasnov, A. A. Dmitriev, N. N. Volchenko, T. V. Danilova, A. F. Sadritdinova, A. V. Snezhkina, N. V. Melnikova, M. S. Fedorova, V. A. Lakunina, A. A. Belova, B. Y. Alekseev, A. D. Kaprin, A. V. Kudryavtseva
Format: Article
Language:Russian
Published: Russian Academy of Sciences, Tomsk National Research Medical Center 2016-02-01
Series:Сибирский онкологический журнал
Subjects:
Online Access:https://www.siboncoj.ru/jour/article/view/286
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author G. S. Krasnov
A. A. Dmitriev
N. N. Volchenko
T. V. Danilova
A. F. Sadritdinova
A. V. Snezhkina
N. V. Melnikova
M. S. Fedorova
V. A. Lakunina
A. A. Belova
B. Y. Alekseev
A. D. Kaprin
A. V. Kudryavtseva
author_facet G. S. Krasnov
A. A. Dmitriev
N. N. Volchenko
T. V. Danilova
A. F. Sadritdinova
A. V. Snezhkina
N. V. Melnikova
M. S. Fedorova
V. A. Lakunina
A. A. Belova
B. Y. Alekseev
A. D. Kaprin
A. V. Kudryavtseva
author_sort G. S. Krasnov
collection DOAJ
description Androgenic pathway plays a pivotal role in the development of benign and malignant prostate tumors. Most of the prostate neoplasms are hormone-dependent at the time of diagnosis. Therapeutic interventions aimed at reducing the level of testosterone in the blood allow to stop progression of the disease. But over time, the tumor almost inevitably starts to progress, moving in the castration-resistant state (CRPC), representing a serious problem of oncourology. In recent years, the possibility of CRRPC therapy increased significantly – there was developed a number of new drugs that effectively inhibit the development of castration-resistant tumors and significantly push back the start of chemotherapy. This review describes the major drug targets and mechanisms of action of abiraterone, enzalutamide, galeterone, VT-464 and other approved and promising CRPC therapies.
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spelling doaj.art-aed37ab4fd6d4f0bbd5f2ace0d68794b2025-03-02T11:16:06ZrusRussian Academy of Sciences, Tomsk National Research Medical CenterСибирский онкологический журнал1814-48612312-31682016-02-01064553286MAIN MOLECULAR TARGETS FOR PROSTATE CANCER THERAPYG. S. Krasnov0A. A. Dmitriev1N. N. Volchenko2T. V. Danilova3A. F. Sadritdinova4A. V. Snezhkina5N. V. Melnikova6M. S. Fedorova7V. A. Lakunina8A. A. Belova9B. Y. Alekseev10A. D. Kaprin11A. V. Kudryavtseva12Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow P.A. Herzen Moscow Cancer Research Institute, Ministry of Healthcare of the Russian Federation, Moscow V. N. Orekhovich Institute of Biomedical Chemistry of the Russian Academy of Medical Sciences, MoscowP.A. Herzen Moscow Cancer Research Institute, Ministry of Healthcare of the Russian Federation, Moscow V. N. Orekhovich Institute of Biomedical Chemistry of the Russian Academy of Medical Sciences, MoscowV. N. Orekhovich Institute of Biomedical Chemistry of the Russian Academy of Medical Sciences, MoscowV. N. Orekhovich Institute of Biomedical Chemistry of the Russian Academy of Medical Sciences, MoscowEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, MoscowEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, MoscowEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, MoscowEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, MoscowEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, MoscowEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, MoscowP.A. Herzen Moscow Cancer Research Institute, Ministry of Healthcare of the Russian Federation, MoscowP.A. Herzen Moscow Cancer Research Institute, Ministry of Healthcare of the Russian Federation, MoscowEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow P.A. Herzen Moscow Cancer Research Institute, Ministry of Healthcare of the Russian Federation, MoscowAndrogenic pathway plays a pivotal role in the development of benign and malignant prostate tumors. Most of the prostate neoplasms are hormone-dependent at the time of diagnosis. Therapeutic interventions aimed at reducing the level of testosterone in the blood allow to stop progression of the disease. But over time, the tumor almost inevitably starts to progress, moving in the castration-resistant state (CRPC), representing a serious problem of oncourology. In recent years, the possibility of CRRPC therapy increased significantly – there was developed a number of new drugs that effectively inhibit the development of castration-resistant tumors and significantly push back the start of chemotherapy. This review describes the major drug targets and mechanisms of action of abiraterone, enzalutamide, galeterone, VT-464 and other approved and promising CRPC therapies.https://www.siboncoj.ru/jour/article/view/286castrate resistant prostate cancerandrogen receptorabirateroneenzalutamidemv3100galeteronevt-464cyp17а1
spellingShingle G. S. Krasnov
A. A. Dmitriev
N. N. Volchenko
T. V. Danilova
A. F. Sadritdinova
A. V. Snezhkina
N. V. Melnikova
M. S. Fedorova
V. A. Lakunina
A. A. Belova
B. Y. Alekseev
A. D. Kaprin
A. V. Kudryavtseva
MAIN MOLECULAR TARGETS FOR PROSTATE CANCER THERAPY
Сибирский онкологический журнал
castrate resistant prostate cancer
androgen receptor
abiraterone
enzalutamide
mv3100
galeterone
vt-464
cyp17а1
title MAIN MOLECULAR TARGETS FOR PROSTATE CANCER THERAPY
title_full MAIN MOLECULAR TARGETS FOR PROSTATE CANCER THERAPY
title_fullStr MAIN MOLECULAR TARGETS FOR PROSTATE CANCER THERAPY
title_full_unstemmed MAIN MOLECULAR TARGETS FOR PROSTATE CANCER THERAPY
title_short MAIN MOLECULAR TARGETS FOR PROSTATE CANCER THERAPY
title_sort main molecular targets for prostate cancer therapy
topic castrate resistant prostate cancer
androgen receptor
abiraterone
enzalutamide
mv3100
galeterone
vt-464
cyp17а1
url https://www.siboncoj.ru/jour/article/view/286
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