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<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">actabiomedica</journal-id><journal-title-group><journal-title xml:lang="ru">Acta Biomedica Scientifica</journal-title><trans-title-group xml:lang="en"><trans-title>Acta Biomedica Scientifica</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2541-9420</issn><issn pub-type="epub">2587-9596</issn><publisher><publisher-name>Scientific Centre for Family Health and Human Reproduction Problems</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">actabiomedica-869</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>ОБЗОРЫ ЛИТЕРАТУРЫ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>REVIEWS OF LITERATURE</subject></subj-group></article-categories><title-group><article-title>МОЛЕКУЛЯРНЫЕ МЕХАНИЗМЫ КАНЦЕРОГЕНЕЗА ЭНДОМЕТРИЯ</article-title><trans-title-group xml:lang="en"><trans-title>MOLECULAR MECHANISMS OF ENDOMETRIAL CARCINOMA</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Гуляева</surname><given-names>Л. Ф.</given-names></name><name name-style="western" xml:lang="en"><surname>Gulyaeva</surname><given-names>L. F.</given-names></name></name-alternatives><email xlink:type="simple">gulyaeva@soramn.ru,lfgulyaeva@ngs.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Красильников</surname><given-names>С. Э.</given-names></name><name name-style="western" xml:lang="en"><surname>Krasilnikov</surname><given-names>S. E.</given-names></name></name-alternatives><email xlink:type="simple">krasilnikov@ngs.ru</email><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФГБУ Институт молекулярной биологии и биофизики СО РАМН; Новосибирский государственный университет</institution></aff><aff xml:lang="en"><institution>Institute of Molecular Biology and Biophysics, Siberian Branch of Russian Academy of Medical Sciences; Novosibirsk State University</institution></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Новосибирский государственный университет; Областной онкологический диспансер</institution></aff><aff xml:lang="en"><institution>Novosibirsk State University; Novosibirsk Regional Oncological Hospital</institution></aff></aff-alternatives><pub-date pub-type="collection"><year>2012</year></pub-date><pub-date pub-type="epub"><day>28</day><month>05</month><year>2012</year></pub-date><volume>0</volume><issue>3(1)</issue><fpage>110</fpage><lpage>115</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Гуляева Л.Ф., Красильников С.Э., 2012</copyright-statement><copyright-year>2012</copyright-year><copyright-holder xml:lang="ru">Гуляева Л.Ф., Красильников С.Э.</copyright-holder><copyright-holder xml:lang="en">Gulyaeva L.F., Krasilnikov S.E.</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.actabiomedica.ru/jour/article/view/869">https://www.actabiomedica.ru/jour/article/view/869</self-uri><abstract><p>Рассмотрены молекулярно-биологические аспекты канцерогенеза эндометрия с анализом научной литературы и собственных экспериментальных данных. Показано, что в этот процесс вовлечены как классические пути сигнальной трансдукции PI3K, Wnt, Bcl-2-регулируемый апоптоз, так и гормональные пути передачи сигнала от ERα к генам-мишеням. Выявлено почти 6-кратное усиление экспрессии гена ингибитора апоптоза Bcl-2 в злокачественных опухолях эндометрия по сравнению с неопухолевой тканью. Уровень экспрессии гена ERα в половине случаев рака эндометрия был выше в опухолевой ткани по сравнению с нетрансформированной тканью. Матричные металлопротеиназы ММР-3, ММР-9, а также ген ангиогенеза Il-8 экспрессируются, главным образом, в злокачественных тканях эндометрия, но не в доброкачественных, что делает их перспективными кандидатами для характеристики опухолей матки. Таким образом, гены Bcl-2, IL8, ERα и MMPs могут быть маркерами канцерогенеза эндометрия в совокупности с такими белками PI3K- и Wnt- сигнальных путей, как PTEN и β-катенин.</p></abstract><trans-abstract xml:lang="en"><p>Molecular aspects of carcinogenesis of endometrium with analysis of scientific literature and own experimental data are considered. It was shown that in this process are involved as well classical signal transduction pathways like PI3K, Wnt, Bcl-2-regulated apoptosis as hormonal pathways from ERα to target genes. Gene expression of apoptosis inhibitor Bcl-2 was in 6 folds higher in malignant tumors in comparison with non cancer tissue. Expression level of ERα gene was higher in cancer tissue than in adjacent non-tumor endometrium. Matrix metallo-proteinases MMR-3, MMR-9 and angiogenesis gene Il-8 expressed mainly in malignant endometrial tissues, but not in non-cancer tissues that considers these genes as suitable candidates for the characteristic of endometrial carcinoma. Thus, Bcl-2, IL8, ERα and MMPs 2 proteins can be appropriate markers of endometrial carcinoma together with the members of PI3K- and Wnt-signal pathways like PTEN and β-catenin.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>рак эндометрия</kwd><kwd>сигнальная трансдукция</kwd><kwd>молекулярные маркеры</kwd><kwd>гены апоптоза Bcl-2</kwd><kwd>гены ангиогенеза IL8 и MMPs</kwd></kwd-group><kwd-group xml:lang="en"><kwd>ERα</kwd><kwd>BAX</kwd><kwd>cancer of endometrium</kwd><kwd>signal transduction</kwd><kwd>molecular markers</kwd><kwd>ERα</kwd><kwd>apoptosis genes Bcl-2 and BAX</kwd><kwd>angiogenesis genes IL8 and MMPs</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Гуляева Л.Ф., Красильников С.Э. 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