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<article article-type="research-article" dtd-version="1.2" xml:lang="ru" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink"><front><journal-meta><journal-id journal-id-type="issn">2658-6533</journal-id><journal-title-group><journal-title>Research Results in Biomedicine</journal-title></journal-title-group><issn pub-type="epub">2658-6533</issn></journal-meta><article-meta><article-id pub-id-type="doi">10.18413/2658-6533-2024-10-2-0-9</article-id><article-id pub-id-type="publisher-id">3426</article-id><article-categories><subj-group subj-group-type="heading"><subject>Medicine (miscellaneous)</subject></subj-group></article-categories><title-group><article-title>&lt;strong&gt;Differential expression of CYP19A1 and lncRNA-CTBP1-AS in the granulosa cells of women with polycystic ovary syndrome&lt;/strong&gt;&lt;br /&gt;
&amp;nbsp;</article-title><trans-title-group xml:lang="en"><trans-title>&lt;strong&gt;Differential expression of CYP19A1 and lncRNA-CTBP1-AS in the granulosa cells of women with polycystic ovary syndrome&lt;/strong&gt;&lt;br /&gt;
&amp;nbsp;</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="ru"><surname>Ali</surname><given-names>Ruba M.</given-names></name><name xml:lang="en"><surname>Ali</surname><given-names>Ruba M.</given-names></name></name-alternatives><email>ruba.m.ali@mail.ru</email></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="ru"><surname>Lomteva</surname><given-names>Svetlana V.</given-names></name><name xml:lang="en"><surname>Lomteva</surname><given-names>Svetlana V.</given-names></name></name-alternatives><email>embryolab61@gmail.com</email></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="ru"><surname>Aleksandrova</surname><given-names>Anzhela A.</given-names></name><name xml:lang="en"><surname>Aleksandrova</surname><given-names>Anzhela A.</given-names></name></name-alternatives><email>aalexsandrova@mail.ru</email></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="ru"><surname>Sagamonova</surname><given-names>Karina Y.</given-names></name><name xml:lang="en"><surname>Sagamonova</surname><given-names>Karina Y.</given-names></name></name-alternatives><email>k.sagamonova@mail.ru</email></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="ru"><surname>Sagamonov</surname><given-names>Artur S.</given-names></name><name xml:lang="en"><surname>Sagamonov</surname><given-names>Artur S.</given-names></name></name-alternatives><email>a.sagamonov@gmail.com</email></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="ru"><surname>Ammar</surname><given-names>Manar N.A.</given-names></name><name xml:lang="en"><surname>Ammar</surname><given-names>Manar N.A.</given-names></name></name-alternatives><email>manarammarnour@gmail.com</email></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="ru"><surname>Shkurat</surname><given-names>Tatiana P.</given-names></name><name xml:lang="en"><surname>Shkurat</surname><given-names>Tatiana P.</given-names></name></name-alternatives><email>tshkurat@yandex.ru</email></contrib></contrib-group><pub-date pub-type="epub"><year>2024</year></pub-date><volume>10</volume><issue>2</issue><fpage>0</fpage><lpage>0</lpage><self-uri content-type="pdf" xlink:href="/media/medicine/2024/2/Биомедицинские_исследования-123-133.pdf" /><abstract xml:lang="ru"><p>Background: Hyperandrogenism is the basic indicator of polycystic ovarian syndrome (PCOS) and a key factor in its pathological processes. Patients with PCOS have higher testosterone levels along with a decline in the estradiol/testosterone ratio, which may indicate an aromatase dysfunction. The aim of the study: Investigating the expression levels of CYP19A1 and lncRNA-CTBP1-AS in the granulosa cells (GCs) of women with and without PCOS. Materials and methods: We compared the expression levels of CYP19A1 and lncRNA-CTBP1-AS in granulosa cells from 16 PCOS patients and 20 controls who underwent assisted reproductive technology (ART) treatment at the Center for Human Reproduction and IVF (Rostov-on-Don, Russia) using quantitative real-time PCR. Results: We observed a significant downregulation of CYP19A1 expression in the GCs of PCOS patients, with expression levels approximately 4.7 times lower compared to the control group. Furthermore, we found a positive correlation between CYP19A1 expression and the E2/T ratio in PCOS patients. Conversely, PCOS patients exhibited a remarkable upregulation of CTBP1-AS expression in their GCs, with levels up to 23 times higher than those in the control group. Importantly, we also identified a significant negative correlation between the expression level of CTBP1-AS and CYP19A1 in the GCs of PCOS patients. Conclusion: Our results indicate a potential regulatory role of CTBP1-AS in CYP19A1 expression and suggest its involvement in the pathogenesis of PCOS</p></abstract><trans-abstract xml:lang="en"><p>Background: Hyperandrogenism is the basic indicator of polycystic ovarian syndrome (PCOS) and a key factor in its pathological processes. Patients with PCOS have higher testosterone levels along with a decline in the estradiol/testosterone ratio, which may indicate an aromatase dysfunction. The aim of the study: Investigating the expression levels of CYP19A1 and lncRNA-CTBP1-AS in the granulosa cells (GCs) of women with and without PCOS. Materials and methods: We compared the expression levels of CYP19A1 and lncRNA-CTBP1-AS in granulosa cells from 16 PCOS patients and 20 controls who underwent assisted reproductive technology (ART) treatment at the Center for Human Reproduction and IVF (Rostov-on-Don, Russia) using quantitative real-time PCR. Results: We observed a significant downregulation of CYP19A1 expression in the GCs of PCOS patients, with expression levels approximately 4.7 times lower compared to the control group. Furthermore, we found a positive correlation between CYP19A1 expression and the E2/T ratio in PCOS patients. Conversely, PCOS patients exhibited a remarkable upregulation of CTBP1-AS expression in their GCs, with levels up to 23 times higher than those in the control group. Importantly, we also identified a significant negative correlation between the expression level of CTBP1-AS and CYP19A1 in the GCs of PCOS patients. Conclusion: Our results indicate a potential regulatory role of CTBP1-AS in CYP19A1 expression and suggest its involvement in the pathogenesis of PCOS</p></trans-abstract><kwd-group xml:lang="ru"><kwd>PCOS</kwd><kwd>Polycystic ovarian Syndrome</kwd><kwd>LncRNA</kwd><kwd>CYP19A1</kwd><kwd>CTBP1-AS</kwd><kwd>gene expression</kwd></kwd-group><kwd-group xml:lang="en"><kwd>PCOS</kwd><kwd>Polycystic ovarian Syndrome</kwd><kwd>LncRNA</kwd><kwd>CYP19A1</kwd><kwd>CTBP1-AS</kwd><kwd>gene expression</kwd></kwd-group></article-meta></front><back><ref-list><title>Список литературы</title><ref id="B1"><mixed-citation>Deswal R, Narwal V, Dang A, et al. The Prevalence of Polycystic Ovary Syndrome: A Brief Systematic Review. Journal of Human Reproductive Sciences. 2020;13(4):261-271. DOI: https://doi.org/10.4103/jhrs.JHRS_95_18</mixed-citation></ref><ref id="B2"><mixed-citation>Coll&amp;eacute;e J, Mawet M, Tebache L, et al. 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