<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.3 20210610//EN" "JATS-journalpublishing1-3.dtd">
<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">safetyrisk</journal-id><journal-title-group><journal-title xml:lang="ru">Безопасность и риск фармакотерапии</journal-title><trans-title-group xml:lang="en"><trans-title>Safety and Risk of Pharmacotherapy</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2312-7821</issn><issn pub-type="epub">2619-1164</issn><publisher><publisher-name>Federal State Budgetary Institution ‘Scientific Centre for Expert Evaluation of Medicinal Products’ of the Ministry of Health of the Russian Federation (FSBI ‘SCEEMP’)</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.30895/2312-7821-2026-14-1-78-89</article-id><article-id custom-type="elpub" pub-id-type="custom">safetyrisk-522</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ГЛАВНАЯ ТЕМА: ЭВОЛЮЦИЯ ФАРМАКОНАДЗОРА: ИНТЕГРАЦИЯ НОВЫХ ИСТОЧНИКОВ ДАННЫХ, ПОПУЛЯЦИОННЫХ ИCСЛЕДОВАНИЙ И ПРЕДИКТИВНЫХ ТЕХНОЛОГИЙ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>MAIN TOPIC: EVOLUTION OF PHARMACOVIGILANCE: INTEGRATING NEW DATA SOURCES,  POPULATION STUDIES AND PREDICTIVE TECHNOLOGIES</subject></subj-group></article-categories><title-group><article-title>Гонадотропин-рилизинг-гормон и органы мочевыделительной системы: анализ противоречивых данных исследований эффективности и безопасности (обзор)</article-title><trans-title-group xml:lang="en"><trans-title>Gonadotropin-Releasing Hormone and the Urinary System: Analyzing Contradictory Findings of Efficacy and Safety Studies (Review)</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-8182-5084</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Майбородин</surname><given-names>И. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Maiborodin</surname><given-names>I. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Майбородин Игорь Валентинович, д-р мед. наук, профессор</p><p>пр-т Академика Лаврентьева, д. 8, г. Новосибирск, 630090;ул. Николаева, д. 12/3, г. Новосибирск, 630090</p></bio><bio xml:lang="en"><p>Igor V. Maiborodin, Dr. Sci. (Med.), Professor</p><p>8 Academician Lavrentyev Ave, Novosibirsk 630090; 12/3 Nikolaev St., Novosibirsk 630090</p></bio><email xlink:type="simple">imai@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0009-0008-4140-3531</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Шеплев</surname><given-names>Б. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Sheplev</surname><given-names>B. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Шеплев Борис Валентинович, д-р мед. наук</p><p>ул. Николаева, д. 12/3, г. Новосибирск, 630090</p></bio><bio xml:lang="en"><p>Boris V. Sheplev, Dr. Sci. (Med.)</p><p>12/3 Nikolaev St., Novosibirsk 630090</p></bio><email xlink:type="simple">shepa@icloud.com</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-2161-6061</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Черноморцева</surname><given-names>Е. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Chernomortseva</surname><given-names>E. S.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Черноморцева Елена Станиславовна, д-р мед. наук, профессор</p><p>ул. Александра Невского, д. 14, г. Калининград, 236016</p></bio><bio xml:lang="en"><p>Elena S. Chernomortseva, Dr. Sci. (Med.), Professor</p><p>14 Alexander Nevsky St., Kaliningrad 236016</p></bio><email xlink:type="simple">cheses11@rambler.ru</email><xref ref-type="aff" rid="aff-3"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0009-0001-8366-2346</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Федина</surname><given-names>И. Ю.</given-names></name><name name-style="western" xml:lang="en"><surname>Fedina</surname><given-names>I. Yu.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Федина Инна Юрьевна, канд. мед. наук, доцент</p><p>пр-т Ленина, д. 40, г. Барнаул, 656038</p></bio><bio xml:lang="en"><p>Inna Yu. Fedina, Cand. Sci. (Med.), Associate Professor</p><p>40 Lenin Ave, Barnaul 656038</p></bio><email xlink:type="simple">infedina@yandex.ru</email><xref ref-type="aff" rid="aff-4"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-5169-6373</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Майбородина</surname><given-names>В. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Maiborodina</surname><given-names>V. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Майбородина Виталина Игоревна, д-р мед. наук</p><p>пр-т Академика Лаврентьева, д. 8, г. Новосибирск, 630090</p></bio><bio xml:lang="en"><p>Vitalina I. Maiborodina, Dr. Sci. (Med.)</p><p>8 Academician Lavrentyev Ave, Novosibirsk 630090</p></bio><email xlink:type="simple">mai_@mail.ru</email><xref ref-type="aff" rid="aff-5"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Федеральное государственное бюджетное учреждение науки «Институт химической биологии и фундаментальной медицины» Сибирского отделения Российской академии наук;&#13;
Частное образовательное учреждение высшего образования «Новосибирский медико-стоматологический институт Дентмастер»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences;&#13;
Novosibirsk Medical and Dental Institute Dentmaster</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Частное образовательное учреждение высшего образования «Новосибирский медико-стоматологический институт Дентмастер»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Novosibirsk Medical and Dental Institute Dentmaster</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-3"><aff xml:lang="ru"><institution>Федеральное государственное автономное образовательное учреждение высшего образования «Балтийский федеральный университет имени Иммануила Канта»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Immanuel Kant Baltic Federal University</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-4"><aff xml:lang="ru"><institution>Федеральное государственное бюджетное учреждение высшего образования «Алтайский государственный медицинский университет» Министерства здравоохранения Российской Федерации</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Altay State Medical University</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-5"><aff xml:lang="ru"><institution>Федеральное государственное бюджетное учреждение науки «Институт химической биологии и фундаментальной медицины» Сибирского отделения Российской академии наук</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2026</year></pub-date><pub-date pub-type="epub"><day>31</day><month>03</month><year>2026</year></pub-date><volume>14</volume><issue>1</issue><fpage>78</fpage><lpage>89</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Майбородин И.В., Шеплев Б.В., Черноморцева Е.С., Федина И.Ю., Майбородина В.И., 2026</copyright-statement><copyright-year>2026</copyright-year><copyright-holder xml:lang="ru">Майбородин И.В., Шеплев Б.В., Черноморцева Е.С., Федина И.Ю., Майбородина В.И.</copyright-holder><copyright-holder xml:lang="en">Maiborodin I.V., Sheplev B.V., Chernomortseva E.S., Fedina I.Y., Maiborodina V.I.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://www.risksafety.ru/jour/article/view/522">https://www.risksafety.ru/jour/article/view/522</self-uri><abstract><sec><title>ВВЕДЕНИЕ</title><p>ВВЕДЕНИЕ. Препараты гонадотропин-рилизинг-гормона (ГнРГ) применяют при заболеваниях органов репродукции, как женских (вызывают временную медикаментозную менопаузу), так и мужских (с целью супрессии функций при доброкачественных и злокачественных заболеваниях). Половая и мочевыделительная системы тесно связаны в онто- и филогенезе. Обобщение и критический анализ имеющихся данных о влиянии препаратов ГнРГ на органы мочевыделительной системы позволит оценить имеющуюся информацию и определить направления дальнейших исследований.</p></sec><sec><title>ЦЕЛЬ</title><p>ЦЕЛЬ. Систематизация имеющихся данных о пользе и рисках терапии ГнРГ в отношении мочевыделительной системы для планирования дальнейших исследований и разработки стратегий терапии.</p></sec><sec><title>ОБСУЖДЕНИЕ</title><p>ОБСУЖДЕНИЕ. Анализ результатов доклинических и клинических исследований показал, что ГнРГ и его метаболиты выводятся из организма преимущественно через почки. Препараты ГнРГ негативно влияют на функции и структуру почек: возможно развитие нефролитиаза вследствие нарушений кальциевого обмена, описаны случаи острого поражения почек вплоть до острой недостаточности. Структуры мочевого пузыря содержат рецепторы ГнРГ, что определяет высокий уровень связывания ГнРГ с его клетками. Высокие уровни ГнРГ и рецепторов ГнРГ при раке мочевого пузыря ассоциированы с повышением общей выживаемости у мужчин и ее снижением у женщин. Высокая экспрессия рецепторов ГнРГ на клеточных элементах рака определяет успешность применения препаратов ГнРГ для терапии новообразований мочевого пузыря. Аналоги ГнРГ оказывают положительный клинический эффект у женщин с возрастной менопаузальной инконтиненцией, непосредственно влияя на ткани мочевого пузыря, в том числе его сфинктерную систему, и уретру. Однако данные в некоторых рассмотренных статьях недостаточно обоснованы и статистически не подтверждены. В ряде работ сообщалось об отсутствии влияния препаратов ГнРГ на функции почек, уретры, а также на исходы опухолей мочевого пузыря.</p></sec><sec><title>ВЫВОДЫ</title><p>ВЫВОДЫ. Явная недостаточность данных и противоречивость публикаций по каждому из аспектов действия ГнРГ на органы мочевыделительной системы свидетельствует о малой изученности этого вопроса. Необходимо продолжение прикладных и фундаментальных исследований влияния ГнРГ на мочевыводящие пути для оценки соотношения пользы и риска, создания новых, менее токсичных противораковых средств, эффективной профилактики и коррекции нежелательных реакций при гормонотерапии различных заболеваний.</p></sec></abstract><trans-abstract xml:lang="en"><sec><title>INTRODUCTION</title><p>INTRODUCTION. Gonadotropin-releasing hormone (GnRH) products are used to treat reproductive system disorders both in females (for temporary medically induced menopause) and males (in order to suppress certain functions in benign and malignant diseases). The urinary and reproductive systems are closely linked in their ontogenesis and phylogenesis. A summary and critical analysis of the existing data will allow us to assess the effects of GnRH products on the urinary system and identify areas for further research.</p></sec><sec><title>AIM</title><p>AIM. This study aimed to identify benefits and risks of GnRH therapy for the urinary system in order to optimize hormone therapy in various conditions.</p></sec><sec><title>DISCUSSION</title><p>DISCUSSION. Analysed preclinical and clinical studies showed that GnRH and its metabolites are primarily excreted by the kidneys. GnRH therapy affects the renal system: nephrolithiasis may develop due to calcium olism disorders; cases of acute kidney injury, including acute renal failure, have been reported as well. Bladder structures include GnRH receptors, resulting in high GnRH binding to bladder cells and effective GnRH therapy. However, there are sex-specific differences; high GnRH and its receptors in bladder cancer are associated with better overall survival in men. High expression of GnRH receptors on cancer cells determines the success of GnRH therapy in the bladder tumours. GnRH analogues show a positive clinical effect in women with age-related menopausal incontinence, directly influencing bladder tissue, the sphincter system, and urethra. However, the data in some of the reviewed articles were insufficiently substantiated and lacked statistical validation. A number of studies reported no effect of GnRH therapy on renal and urethral function, or on bladder tumour outcomes.</p></sec><sec><title>CONCLUSIONS</title><p>CONCLUSIONS. The apparent lack of data and inconsistent publications on each aspect of GnRH influencing the urinary system indicate a paucity of research for this issue. Further applied and fundamental research of GnRH effects on the urinary tract is warranted to assess the benefit-risk ratio, develop less toxic anticancer agents, and effectively prevent and treat adverse reactions during hormone therapy for various diseases.</p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>гонадотропин-рилизинг-гормон</kwd><kwd>мочевыделительная система</kwd><kwd>почки</kwd><kwd>мочевой пузырь</kwd><kwd>уретра</kwd><kwd>острое поражение почек</kwd><kwd>новообразования мочевого пузыря</kwd><kwd>мочекаменная болезнь</kwd><kwd>нарушения&#13;
кальциевого обмена</kwd><kwd>недержание мочи</kwd><kwd>менопауза</kwd><kwd>нарративный обзор</kwd></kwd-group><kwd-group xml:lang="en"><kwd>gonadotropin-releasing hormone</kwd><kwd>GnRH</kwd><kwd>urinary system</kwd><kwd>kidneys</kwd><kwd>bladder</kwd><kwd>urethra</kwd><kwd>acute kidney injury</kwd><kwd>urinary bladder neoplasms</kwd><kwd>nephrolithiasis</kwd><kwd>calcium metabolism disorders</kwd><kwd>urinary incontinence</kwd><kwd>menopause</kwd><kwd>narrative review</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Исследование поддержано в рамках государственного задания ФГБУН ИХБФМ СО РАН «Фундаментальные основы сохранения здоровья нации» № FWGN-2025-0019. Финансовой поддержки со стороны компаний — производителей оборудования, реактивов и лекарственных препаратов авторы не получали</funding-statement><funding-statement xml:lang="en">The study was supported by the publicly funded research project by Institute of chemical biology and fundamental medicine (No. FWGN-2025-0019). The authors did not receive any financial support from companies manufacturing equipment, reagents, and medicinal products</funding-statement></funding-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Tsutsui K, Ubuka T. How to contribute to the progress of neuroendocrinology: Discovery of GnIH and progress of GnIH research. Front Endocrinol (Lausanne). 2018;9:662. https://doi.org/10.3389/fendo.2018.00662</mixed-citation><mixed-citation xml:lang="en">Tsutsui K, Ubuka T. How to contribute to the progress of neuroendocrinology: Discovery of GnIH and progress of GnIH research. Front Endocrinol (Lausanne). 2018;9:662. https://doi.org/10.3389/fendo.2018.00662</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Schally AV, Guillemin R. Isolation and chemical characterization of a beta-CRF from pig posterior pituitary glands. Proc Soc Exp Biol Med. 1963;112:1014–7. https://doi.org/10.3181/00379727-112-28238</mixed-citation><mixed-citation xml:lang="en">Schally AV, Guillemin R. Isolation and chemical characterization of a beta-CRF from pig posterior pituitary glands. Proc Soc Exp Biol Med. 1963;112:1014–7. https://doi.org/10.3181/00379727-112-28238</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Stamatiades GA, Toufaily C, Kim HK, et al. Deletion of Gαq/11 or Gαs proteins in gonadotropes differentially affects gonadotropin production and secretion in mice. Endocrinology. 2022;163(2):bqab247. https://doi.org/10.1210/endocr/bqab247</mixed-citation><mixed-citation xml:lang="en">Stamatiades GA, Toufaily C, Kim HK, et al. Deletion of Gαq/11 or Gαs proteins in gonadotropes differentially affects gonadotropin production and secretion in mice. Endocrinology. 2022;163(2):bqab247. https://doi.org/10.1210/endocr/bqab247</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Schally AV, Coy DH, Arimura A. LH-RH agonists and antagonists. Int J Gynaecol Obstet. 1980;18(5):318–24. https://doi.org/10.1002/j.1879-3479.1980.tb00507.x</mixed-citation><mixed-citation xml:lang="en">Schally AV, Coy DH, Arimura A. LH-RH agonists and antagonists. Int J Gynaecol Obstet. 1980;18(5):318–24. https://doi.org/10.1002/j.1879-3479.1980.tb00507.x</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Sandow J. Clinical applications of LHRH and its analogues. Clin Endocrinol (Oxf). 1983;18(6):571–92. https://doi.org/10.1111/j.1365-2265.1983.tb00595.x</mixed-citation><mixed-citation xml:lang="en">Sandow J. Clinical applications of LHRH and its analogues. Clin Endocrinol (Oxf). 1983;18(6):571–92. https://doi.org/10.1111/j.1365-2265.1983.tb00595.x</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Furr BJ. Pharmacology of the luteinising hormone-releasing hormone (LHRH) analogue. Zoladex Horm Res. 1989;32 Suppl 1:86–92. https://doi.org/10.1159/000181318</mixed-citation><mixed-citation xml:lang="en">Furr BJ. Pharmacology of the luteinising hormone-releasing hormone (LHRH) analogue. Zoladex Horm Res. 1989;32 Suppl 1:86–92. https://doi.org/10.1159/000181318</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Maiborodin IV, Pichigina AK, Maiborodina VI, Lushnikova EL. Physiological aspects of the application of gonadotropin-releasing hormone agonists in obstetric-gynecological clinic and experiment. J Evol Biochem Phys. 2022;58(6):1865–78. https://doi.org/10.1134/S0022093022060163</mixed-citation><mixed-citation xml:lang="en">Maiborodin IV, Pichigina AK, Maiborodina VI, Lushnikova EL. Physiological aspects of the application of gonadotropin-releasing hormone agonists in obstetric-gynecological clinic and experiment. J Evol Biochem Phys. 2022;58(6):1865–78. https://doi.org/10.1134/S0022093022060163</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Майбородин ИВ, Шеплев БВ. Андрологические аспекты эффектов агонистов гонадотропин-рилизинг-гормона в эксперименте и клинике. Acta Biomedica Scientifica. 2024;9(6):85–99. https://doi.org/10.29413/ABS.2024-9.6.9</mixed-citation><mixed-citation xml:lang="en">Maiborodin IV, Sheplev BV. Andrological aspects of the effects of gonadotropin-releasing hormone agonists in experiment and clinic. Acta Biomedica Scientifica. 2024;9(6):85–99 (In Russ.). https://doi.org/10.29413/ABS.2024-9.6.9</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Hao D, Sun L, Hu X, Hao X. 99mTc-LHRH in tumor receptor imaging. Oncol Lett. 2017;14(1):569–78. https://doi.org/10.3892/ol.2017.6246</mixed-citation><mixed-citation xml:lang="en">Hao D, Sun L, Hu X, Hao X. 99mTc-LHRH in tumor receptor imaging. Oncol Lett. 2017;14(1):569–78. https://doi.org/10.3892/ol.2017.6246</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Cardwell AM, Maleki F, Sadeghzadeh N, et al. Evaluation of a New 99mTc-labeled GnRH analogue as a possible imaging agent for prostate cancer detection. Anticancer Agents Med Chem. 2020;20(14):1695–703. https://doi.org/10.2174/1871520620666200619175352</mixed-citation><mixed-citation xml:lang="en">Cardwell AM, Maleki F, Sadeghzadeh N, et al. Evaluation of a New 99mTc-labeled GnRH analogue as a possible imaging agent for prostate cancer detection. Anticancer Agents Med Chem. 2020;20(14):1695–703. https://doi.org/10.2174/1871520620666200619175352</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Farahani AM, Maleki F, Sadeghzadeh N, et al. 99mTc-(EDDA/tricine)-HYNIC-GnRH analogue as a potential imaging probe for diagnosis of prostate cancer. Chem Biol Drug Des. 2020;96(2):850–60. https://doi.org/10.1111/cbdd.13693</mixed-citation><mixed-citation xml:lang="en">Farahani AM, Maleki F, Sadeghzadeh N, et al. 99mTc-(EDDA/tricine)-HYNIC-GnRH analogue as a potential imaging probe for diagnosis of prostate cancer. Chem Biol Drug Des. 2020;96(2):850–60. https://doi.org/10.1111/cbdd.13693</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Zvereva I, Dudko G, Dikunets M. Determination of GnRH and its synthetic analogues’ abuse in doping control: Small bioactive peptide UPLC-MS/MS method extension by addition of in vitro and in vivo metabolism data; evaluation of LH and steroid profile parameter fluctuations as suitable biomarkers. Drug Test Anal. 2018;10(4):711–22. https://doi.org/10.1002/dta.2256</mixed-citation><mixed-citation xml:lang="en">Zvereva I, Dudko G, Dikunets M. Determination of GnRH and its synthetic analogues’ abuse in doping control: Small bioactive peptide UPLC-MS/MS method extension by addition of in vitro and in vivo metabolism data; evaluation of LH and steroid profile parameter fluctuations as suitable biomarkers. Drug Test Anal. 2018;10(4):711–22. https://doi.org/10.1002/dta.2256</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Jyrkäs J, Lassila T, Tolonen A. Extrahepatic in vitro metabolism of peptides; comparison of human kidney and intestinal S9 fraction, human plasma and proximal tubule cells, using cyclosporine A, leuprorelin, and cetrorelix as model compounds. J Pharm Biomed Anal. 2023;225:115219. https://doi.org/10.1016/j.jpba.2022.115219</mixed-citation><mixed-citation xml:lang="en">Jyrkäs J, Lassila T, Tolonen A. Extrahepatic in vitro metabolism of peptides; comparison of human kidney and intestinal S9 fraction, human plasma and proximal tubule cells, using cyclosporine A, leuprorelin, and cetrorelix as model compounds. J Pharm Biomed Anal. 2023;225:115219. https://doi.org/10.1016/j.jpba.2022.115219</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Yu Z, Yang J, Huang WJ, et al. Follicle stimulating hormone promotes production of renin through its receptor in juxtaglomerular cells of kidney. Diabetol Metab Syndr. 2022;14:65. https://doi.org/10.1186/s13098-022-00816-x</mixed-citation><mixed-citation xml:lang="en">Yu Z, Yang J, Huang WJ, et al. Follicle stimulating hormone promotes production of renin through its receptor in juxtaglomerular cells of kidney. Diabetol Metab Syndr. 2022;14:65. https://doi.org/10.1186/s13098-022-00816-x</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Teoh JY, Tian XY, Wong CY, et al. Endothelial dysfunction after androgen deprivation therapy and the possible underlying mechanisms. Prostate. 2022;82(1):13–25. https://doi.org/10.1002/pros.24244</mixed-citation><mixed-citation xml:lang="en">Teoh JY, Tian XY, Wong CY, et al. Endothelial dysfunction after androgen deprivation therapy and the possible underlying mechanisms. Prostate. 2022;82(1):13–25. https://doi.org/10.1002/pros.24244</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Busby ER, Sherwood NM. Gonadotropin-releasing hormone receptor (Gnrhr) gene knock out: Normal growth and development of sensory, motor and spatial orientation behavior but altered metabolism in neonatal and prepubertal mice. PLoS One. 2017;12(3):e0174452. https://doi.org/10.1371/journal.pone.0174452</mixed-citation><mixed-citation xml:lang="en">Busby ER, Sherwood NM. Gonadotropin-releasing hormone receptor (Gnrhr) gene knock out: Normal growth and development of sensory, motor and spatial orientation behavior but altered metabolism in neonatal and prepubertal mice. PLoS One. 2017;12(3):e0174452. https://doi.org/10.1371/journal.pone.0174452</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Díaz Convalía EJ, Cano-García MDC, Miján-Ortiz JL, et al. Androgen deprivation therapy in prostate cancer and risk of developing renal calculi: Results of a case-control study. Med Clin (Barc). 2017;148(11):495–7. https://doi.org/10.1016/j.medcli.2017.01.021</mixed-citation><mixed-citation xml:lang="en">Díaz Convalía EJ, Cano-García MDC, Miján-Ortiz JL, et al. Androgen deprivation therapy in prostate cancer and risk of developing renal calculi: Results of a case-control study. Med Clin (Barc). 2017;148(11):495–7. https://doi.org/10.1016/j.medcli.2017.01.021</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Mayrhofer G, Wegner D, Voß T. Urolithiasis bei der langzeitherapie mit GnRH-agonisten bei paraphilien — 3 Fallberichte. Aktuelle Urol. 2016;47(6):487–90 (In German). https://doi.org/10.1055/s-0042-112999</mixed-citation><mixed-citation xml:lang="en">Mayrhofer G, Wegner D, Voß T. Urolithiasis bei der langzeitherapie mit GnRH-agonisten bei paraphilien — 3 Fallberichte. Aktuelle Urol. 2016;47(6):487–90 (In German). https://doi.org/10.1055/s-0042-112999</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Diaz-Convalia E, Arrabal-Polo MA, Cano-Garcia MDC, et al. Risk of renal stone formation in patients treated with luteinising hormone-releasing hormone analogues for prostate cancer: Importance of bone metabolism and urine calcium. Int Urol Nephrol. 2018;50(3):419–25. https://doi.org/10.1007/s11255-018-1793-1</mixed-citation><mixed-citation xml:lang="en">Diaz-Convalia E, Arrabal-Polo MA, Cano-Garcia MDC, et al. Risk of renal stone formation in patients treated with luteinising hormone-releasing hormone analogues for prostate cancer: Importance of bone metabolism and urine calcium. Int Urol Nephrol. 2018;50(3):419–25. https://doi.org/10.1007/s11255-018-1793-1</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Cardwell CR, O’Sullivan JM, Jain S, et al. Hormone therapy use and the risk of acute kidney injury in patients with prostate cancer: A population-based cohort study. Prostate Cancer Prostatic Dis. 2021;24(4):1055–62. https://doi.org/10.1038/s41391-021-00348-x</mixed-citation><mixed-citation xml:lang="en">Cardwell CR, O’Sullivan JM, Jain S, et al. Hormone therapy use and the risk of acute kidney injury in patients with prostate cancer: A population-based cohort study. Prostate Cancer Prostatic Dis. 2021;24(4):1055–62. https://doi.org/10.1038/s41391-021-00348-x</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Cirkel U, Schweppe KW, Ochs H, Schneider HP. Metabolische effekte und allgemeine nebenwirkungen bei endometriosebehandlung mit einem LHRH-Agonisten. Geburtshilfe Frauenheilkd. 1987;47(3):154–7 (In German). https://doi.org/10.1055/s-2008-1035798</mixed-citation><mixed-citation xml:lang="en">Cirkel U, Schweppe KW, Ochs H, Schneider HP. Metabolische effekte und allgemeine nebenwirkungen bei endometriosebehandlung mit einem LHRH-Agonisten. Geburtshilfe Frauenheilkd. 1987;47(3):154–7 (In German). https://doi.org/10.1055/s-2008-1035798</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Cirkel U, Schweppe KW, Ochs H, et al. LH-RH agonist (buserelin): Treatment of endometriosis. Clinical, laparoscopic, endocrine and metabolic evaluation. Arch Gynecol Obstet. 1989;246(3):139–51. https://doi.org/10.1007/BF00934075</mixed-citation><mixed-citation xml:lang="en">Cirkel U, Schweppe KW, Ochs H, et al. LH-RH agonist (buserelin): Treatment of endometriosis. Clinical, laparoscopic, endocrine and metabolic evaluation. Arch Gynecol Obstet. 1989;246(3):139–51. https://doi.org/10.1007/BF00934075</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Raitz von Frentz M, Schweppe KW. Ovarielle suppression durch das GnRH-analogon Buserelin zur behandlung der endometriose. Klinische, biochemische und pelviskopische untersuchungen. -Geburtshilfe Frauenheilkd. 1990;50(8):634–9 (In German). https://doi.org/10.1055/s-2008-1026515</mixed-citation><mixed-citation xml:lang="en">Raitz von Frentz M, Schweppe KW. Ovarielle suppression durch das GnRH-analogon Buserelin zur behandlung der endometriose. Klinische, biochemische und pelviskopische untersuchungen. -Geburtshilfe Frauenheilkd. 1990;50(8):634–9 (In German). https://doi.org/10.1055/s-2008-1026515</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Chen SC, Ng HT, Tzeng CR, et al. Buserelin treatment of endometriosis in Chinese women. Zhonghua Yi Xue Za Zhi (Taipei). 1991;47(1):1–6. https://pubmed.ncbi.nlm.nih.gov/1848456</mixed-citation><mixed-citation xml:lang="en">Chen SC, Ng HT, Tzeng CR, et al. Buserelin treatment of endometriosis in Chinese women. Zhonghua Yi Xue Za Zhi (Taipei). 1991;47(1):1–6. https://pubmed.ncbi.nlm.nih.gov/1848456</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Barrington JW, Roberts A. Acute renal failure precipitated by luteinizing-hormone releasing hormone analogue for the treatment of endometriosis. Br J Urol. 1994;74(5):672. https://doi.org/10.1111/j.1464-410x.1994.tb09206.x</mixed-citation><mixed-citation xml:lang="en">Barrington JW, Roberts A. Acute renal failure precipitated by luteinizing-hormone releasing hormone analogue for the treatment of endometriosis. Br J Urol. 1994;74(5):672. https://doi.org/10.1111/j.1464-410x.1994.tb09206.x</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Khalil MA, Ghazni MS, Tan J, et al. Spontaneous bacterial peritonitis and anasarca in a female patient with ovarian hyperstimulation syndrome complicated by respiratory and kidney failure. Case Rep Gastroenterol. 2016;10(2):423–30. https://doi.org/10.1159/000446766</mixed-citation><mixed-citation xml:lang="en">Khalil MA, Ghazni MS, Tan J, et al. Spontaneous bacterial peritonitis and anasarca in a female patient with ovarian hyperstimulation syndrome complicated by respiratory and kidney failure. Case Rep Gastroenterol. 2016;10(2):423–30. https://doi.org/10.1159/000446766</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Pereira N, Lekovich JP, Kligman I, Rosenwaks Z. Severe ovarian hyperstimulation syndrome after combined GnRH-agonist and low-dose human chorionic gonadotropin trigger in a patient with a single kidney. Gynecol Endocrinol. 2017;33(8):593–7. https://doi.org/10.1080/09513590.2017.1318372</mixed-citation><mixed-citation xml:lang="en">Pereira N, Lekovich JP, Kligman I, Rosenwaks Z. Severe ovarian hyperstimulation syndrome after combined GnRH-agonist and low-dose human chorionic gonadotropin trigger in a patient with a single kidney. Gynecol Endocrinol. 2017;33(8):593–7. https://doi.org/10.1080/09513590.2017.1318372</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Bakhtiani P, Srivastava R, Geffner M. Puberty today, gone tomorrow: Transient refractory central precocious puberty in a toddler with end-stage kidney disease. Horm Res Paediatr. 2024;97(1):109–15. https://doi.org/10.1159/000536323</mixed-citation><mixed-citation xml:lang="en">Bakhtiani P, Srivastava R, Geffner M. Puberty today, gone tomorrow: Transient refractory central precocious puberty in a toddler with end-stage kidney disease. Horm Res Paediatr. 2024;97(1):109–15. https://doi.org/10.1159/000536323</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Shanehsazzadeh S, Lahooti A, Sadeghi HR, Jalilian AR. Estimation of human effective absorbed dose of 67Ga-cDTPA-gonadorelin based on biodistribution rat data. Nucl Med Commun. 2011;32(1):37–43. https://doi.org/10.1097/MNM.0b013e328340b916</mixed-citation><mixed-citation xml:lang="en">Shanehsazzadeh S, Lahooti A, Sadeghi HR, Jalilian AR. Estimation of human effective absorbed dose of 67Ga-cDTPA-gonadorelin based on biodistribution rat data. Nucl Med Commun. 2011;32(1):37–43. https://doi.org/10.1097/MNM.0b013e328340b916</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Coit VA, Dowell FJ, Evans NP. Neutering affects mRNA expression levels for the LH- and GnRH-receptors in the canine urinary bladder. Theriogenology. 2009;71(2):239–47. https://doi.org/10.1016/j.theriogenology.2008.06.093</mixed-citation><mixed-citation xml:lang="en">Coit VA, Dowell FJ, Evans NP. Neutering affects mRNA expression levels for the LH- and GnRH-receptors in the canine urinary bladder. Theriogenology. 2009;71(2):239–47. https://doi.org/10.1016/j.theriogenology.2008.06.093</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Russo A, Castiglione F, Salonia A, et al. Effects of the gonadotropin-releasing hormone antagonist ganirelix on normal micturition and prostaglandin E(2)-induced detrusor overactivity in conscious female rats. Eur Urol. 2011;59(5):868–74. https://doi.org/10.1016/j.eururo.2010.12.007</mixed-citation><mixed-citation xml:lang="en">Russo A, Castiglione F, Salonia A, et al. Effects of the gonadotropin-releasing hormone antagonist ganirelix on normal micturition and prostaglandin E(2)-induced detrusor overactivity in conscious female rats. Eur Urol. 2011;59(5):868–74. https://doi.org/10.1016/j.eururo.2010.12.007</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Medina-Aguiñaga D, Munoz A, Luna M, et al. Administration of leuprolide acetate, a GnRH agonist, improves urodynamic parameters in ovariectomized rats. Neurourol Urodyn. 2018;37(5):1574–82. https://doi.org/10.1002/nau.23505</mixed-citation><mixed-citation xml:lang="en">Medina-Aguiñaga D, Munoz A, Luna M, et al. Administration of leuprolide acetate, a GnRH agonist, improves urodynamic parameters in ovariectomized rats. Neurourol Urodyn. 2018;37(5):1574–82. https://doi.org/10.1002/nau.23505</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Bujok J, Wincewicz E, Czerski A, Zawadzki W. Influence of ovariohysterectomy and deslorelin acetate on the spontaneous activity of the rabbit urinary bladder in vitro. Theriogenology. 2016;85(3):441–6. https://doi.org/10.1016/j.theriogenology.2015.09.018</mixed-citation><mixed-citation xml:lang="en">Bujok J, Wincewicz E, Czerski A, Zawadzki W. Influence of ovariohysterectomy and deslorelin acetate on the spontaneous activity of the rabbit urinary bladder in vitro. Theriogenology. 2016;85(3):441–6. https://doi.org/10.1016/j.theriogenology.2015.09.018</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Reichler IM, Hubler M, Jöchle W, et al. The effect of GnRH analogs on urinary incontinence after ablation of the ovaries in dogs. Theriogenology. 2003;60(7):1207–16. https://doi.org/10.1016/s0093-691x(02)01368-7</mixed-citation><mixed-citation xml:lang="en">Reichler IM, Hubler M, Jöchle W, et al. The effect of GnRH analogs on urinary incontinence after ablation of the ovaries in dogs. Theriogenology. 2003;60(7):1207–16. https://doi.org/10.1016/s0093-691x(02)01368-7</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Reichler IM, Barth A, Piché CA, et al. Urodynamic parameters and plasma LH/FSH in spayed Beagle bitches before and 8 weeks after GnRH depot analogue treatment. Theriogenology. 2006;66(9):2127–36. https://doi.org/10.1016/j.theriogenology.2006.06.009</mixed-citation><mixed-citation xml:lang="en">Reichler IM, Barth A, Piché CA, et al. Urodynamic parameters and plasma LH/FSH in spayed Beagle bitches before and 8 weeks after GnRH depot analogue treatment. Theriogenology. 2006;66(9):2127–36. https://doi.org/10.1016/j.theriogenology.2006.06.009</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Liang W, Afshar K, Stothers L, Laher I. The influence of ovariectomy and estrogen replacement on voiding patterns and detrusor muscarinic receptor affinity in the rat. Life Sci. 2002;71(3):351–62. https://doi.org/10.1016/s0024-3205(02)01645-4</mixed-citation><mixed-citation xml:lang="en">Liang W, Afshar K, Stothers L, Laher I. The influence of ovariectomy and estrogen replacement on voiding patterns and detrusor muscarinic receptor affinity in the rat. Life Sci. 2002;71(3):351–62. https://doi.org/10.1016/s0024-3205(02)01645-4</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Palacios JL, Luquin S, Quintanar JL, Munoz A. Continuous administration of leuprolide acetate improves urinary function in male rats with severe thoracic spinal cord injury. Life Sci. 2022;310:121113. https://doi.org/10.1016/j.lfs.2022.121113</mixed-citation><mixed-citation xml:lang="en">Palacios JL, Luquin S, Quintanar JL, Munoz A. Continuous administration of leuprolide acetate improves urinary function in male rats with severe thoracic spinal cord injury. Life Sci. 2022;310:121113. https://doi.org/10.1016/j.lfs.2022.121113</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Szabó Z, Dezső B, Fodor K, et al. Expression of luteinizing hormone-releasing hormone (LHRH) and type-I LHRH receptor in transitional cell carcinoma type of human bladder cancer. Molecules. 2021;26(5):1253. https://doi.org/10.3390/molecules26051253</mixed-citation><mixed-citation xml:lang="en">Szabó Z, Dezső B, Fodor K, et al. Expression of luteinizing hormone-releasing hormone (LHRH) and type-I LHRH receptor in transitional cell carcinoma type of human bladder cancer. Molecules. 2021;26(5):1253. https://doi.org/10.3390/molecules26051253</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Szepeshazi K, Schally AV, Keller G, et al. Receptor-targeted therapy of human experimental urinary bladder cancers with cytotoxic LH-RH analog AN-152 [AEZS-108]. Oncotarget. 2012;3(7):686–99. https://doi.org/10.18632/oncotarget.546</mixed-citation><mixed-citation xml:lang="en">Szepeshazi K, Schally AV, Keller G, et al. Receptor-targeted therapy of human experimental urinary bladder cancers with cytotoxic LH-RH analog AN-152 [AEZS-108]. Oncotarget. 2012;3(7):686–99. https://doi.org/10.18632/oncotarget.546</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Engel JB, Tinneberg HR, Rick FG, et al. Targeting of peptide cytotoxins to LHRH receptors for treatment of cancer. Curr Drug Targets. 2016;17(5):488–94. https://doi.org/10.2174/138945011705160303154717</mixed-citation><mixed-citation xml:lang="en">Engel JB, Tinneberg HR, Rick FG, et al. Targeting of peptide cytotoxins to LHRH receptors for treatment of cancer. Curr Drug Targets. 2016;17(5):488–94. https://doi.org/10.2174/138945011705160303154717</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Gründker C, Emons G. The role of gonadotropin-releasing hormone in cancer cell proliferation and metastasis. Front Endocrinol (Lausanne). 2017;8:187. https://doi.org/10.3389/fendo.2017.00187</mixed-citation><mixed-citation xml:lang="en">Gründker C, Emons G. The role of gonadotropin-releasing hormone in cancer cell proliferation and metastasis. Front Endocrinol (Lausanne). 2017;8:187. https://doi.org/10.3389/fendo.2017.00187</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Suo L, Chang X, Xu N, Ji H. The anti-proliferative activity of GnRH through downregulation of the Akt/ERK pathways in pancreatic cancer. Front Endocrinol (Lausanne). 2019;10:370. https://doi.org/10.3389/fendo.2019.00370</mixed-citation><mixed-citation xml:lang="en">Suo L, Chang X, Xu N, Ji H. The anti-proliferative activity of GnRH through downregulation of the Akt/ERK pathways in pancreatic cancer. Front Endocrinol (Lausanne). 2019;10:370. https://doi.org/10.3389/fendo.2019.00370</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Emons G, Gründker C, Günthert AR, et al. GnRH antagonists in the treatment of gynecological and breast cancers. Endocr Relat Cancer. 2003;10(2):291–9. https://doi.org/10.1677/erc.0,0100291</mixed-citation><mixed-citation xml:lang="en">Emons G, Gründker C, Günthert AR, et al. GnRH antagonists in the treatment of gynecological and breast cancers. Endocr Relat Cancer. 2003;10(2):291–9. https://doi.org/10.1677/erc.0,0100291</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">Montagnani Marelli M, Moretti RM, Januszkiewicz-Caulier J, et al. Gonadotropin-releasing hormone (GnRH) receptors in tumors: A new rationale for the therapeutical application of GnRH analogs in cancer patients? Curr Cancer Drug Targets. 2006;6(3):257–69. https://doi.org/10.2174/156800906776842966</mixed-citation><mixed-citation xml:lang="en">Montagnani Marelli M, Moretti RM, Januszkiewicz-Caulier J, et al. Gonadotropin-releasing hormone (GnRH) receptors in tumors: A new rationale for the therapeutical application of GnRH analogs in cancer patients? Curr Cancer Drug Targets. 2006;6(3):257–69. https://doi.org/10.2174/156800906776842966</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">Cheung LW, Wong AS. Gonadotropin-releasing hormone: GnRH receptor signaling in extrapituitary tissues. FEBS J. 2008;275(22):5479–95. https://doi.org/10.1111/j.1742-4658.2008.06677.x</mixed-citation><mixed-citation xml:lang="en">Cheung LW, Wong AS. Gonadotropin-releasing hormone: GnRH receptor signaling in extrapituitary tissues. FEBS J. 2008;275(22):5479–95. https://doi.org/10.1111/j.1742-4658.2008.06677.x</mixed-citation></citation-alternatives></ref><ref id="cit46"><label>46</label><citation-alternatives><mixed-citation xml:lang="ru">So WK, Cheng JC, Poon SL, Leung PC. Gonadotropin-releasing hormone and ovarian cancer: a functional and mechanistic overview. FEBS J. 2008;275(22):5496–511. https://doi.org/10.1111/j.1742-4658.2008.06679.x</mixed-citation><mixed-citation xml:lang="en">So WK, Cheng JC, Poon SL, Leung PC. Gonadotropin-releasing hormone and ovarian cancer: a functional and mechanistic overview. FEBS J. 2008;275(22):5496–511. https://doi.org/10.1111/j.1742-4658.2008.06679.x</mixed-citation></citation-alternatives></ref><ref id="cit47"><label>47</label><citation-alternatives><mixed-citation xml:lang="ru">Wu SC, Kwon D, Jue JS, et al. Androgen suppression therapy is associated with lower recurrence of non-muscle-invasive bladder cancer. Eur Urol Focus. 2021;7(1):142–7. https://doi.org/10.1016/j.euf.2019.04.021</mixed-citation><mixed-citation xml:lang="en">Wu SC, Kwon D, Jue JS, et al. Androgen suppression therapy is associated with lower recurrence of non-muscle-invasive bladder cancer. Eur Urol Focus. 2021;7(1):142–7. https://doi.org/10.1016/j.euf.2019.04.021</mixed-citation></citation-alternatives></ref><ref id="cit48"><label>48</label><citation-alternatives><mixed-citation xml:lang="ru">Kourbanhoussen K, McMartin C, Lodde M, et al. Switching cancers: A systematic review assessing the role of androgen suppressive therapy in bladder cancer. Eur Urol Focus. 2021;7(5):1044–51. https://doi.org/10.1016/j.euf.2020.10.002</mixed-citation><mixed-citation xml:lang="en">Kourbanhoussen K, McMartin C, Lodde M, et al. Switching cancers: A systematic review assessing the role of androgen suppressive therapy in bladder cancer. Eur Urol Focus. 2021;7(5):1044–51. https://doi.org/10.1016/j.euf.2020.10.002</mixed-citation></citation-alternatives></ref><ref id="cit49"><label>49</label><citation-alternatives><mixed-citation xml:lang="ru">Song Y, Qin C, Zhang C, et al. GNRH family genes contributed to gender-specific disparity of bladder cancer prognosis through exerting opposite regulatory roles between males and females. J Cancer Res Clin Oncol. 2023;149(10):6827–40. https://doi.org/10.1007/s00432-023-04640-2</mixed-citation><mixed-citation xml:lang="en">Song Y, Qin C, Zhang C, et al. GNRH family genes contributed to gender-specific disparity of bladder cancer prognosis through exerting opposite regulatory roles between males and females. J Cancer Res Clin Oncol. 2023;149(10):6827–40. https://doi.org/10.1007/s00432-023-04640-2</mixed-citation></citation-alternatives></ref><ref id="cit50"><label>50</label><citation-alternatives><mixed-citation xml:lang="ru">Yikilmaz TN, Ozturk E, Hizli F, et al. Effect of hormonal therapy for volume reduction, lower urinary tract symptom relief and voiding symptoms in prostate cancer: Leuprolide vs goserelin. Urol J. 2019;16(2):157–61. https://doi.org/10.22037/uj.v0i0.4245</mixed-citation><mixed-citation xml:lang="en">Yikilmaz TN, Ozturk E, Hizli F, et al. Effect of hormonal therapy for volume reduction, lower urinary tract symptom relief and voiding symptoms in prostate cancer: Leuprolide vs goserelin. Urol J. 2019;16(2):157–61. https://doi.org/10.22037/uj.v0i0.4245</mixed-citation></citation-alternatives></ref><ref id="cit51"><label>51</label><citation-alternatives><mixed-citation xml:lang="ru">Eriguchi T, Kawamorita N, Hayashi N, et al. High luteinizing hormone weakens urinary continence mechanisms in association with prostaglandin E2 elevation in a postmenopausal rat model. Neurourol Urodyn. 2018;37(4):1294–301. https://doi.org/10.1002/nau.23470</mixed-citation><mixed-citation xml:lang="en">Eriguchi T, Kawamorita N, Hayashi N, et al. High luteinizing hormone weakens urinary continence mechanisms in association with prostaglandin E2 elevation in a postmenopausal rat model. Neurourol Urodyn. 2018;37(4):1294–301. https://doi.org/10.1002/nau.23470</mixed-citation></citation-alternatives></ref><ref id="cit52"><label>52</label><citation-alternatives><mixed-citation xml:lang="ru">Hinerman-Mulroy A, Merrick GS, Butler WM, et al. Androgen deprivation-induced changes in prostate anatomy predict urinary morbidity after permanent interstitial brachytherapy. Int J Radiat Oncol Biol Phys. 2004;59(5):1367–82. https://doi.org/10.1016/j.ijrobp.2004.01.017</mixed-citation><mixed-citation xml:lang="en">Hinerman-Mulroy A, Merrick GS, Butler WM, et al. Androgen deprivation-induced changes in prostate anatomy predict urinary morbidity after permanent interstitial brachytherapy. Int J Radiat Oncol Biol Phys. 2004;59(5):1367–82. https://doi.org/10.1016/j.ijrobp.2004.01.017</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
