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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">medgen</journal-id><journal-title-group><journal-title xml:lang="ru">Медицинская генетика</journal-title><trans-title-group xml:lang="en"><trans-title>Medical Genetics</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2073-7998</issn><publisher><publisher-name>Publishing House «Genius Media» LLC</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.25557/2073-7998.2020.11.73-75</article-id><article-id custom-type="elpub" pub-id-type="custom">medgen-1804</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>КРАТКИЕ СООБЩЕНИЯ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>BRIEF REPORT</subject></subj-group></article-categories><title-group><article-title>Транскриптомика плацентарной ткани: идентификация молекулярных механизмов и мишеней для таргетной терапии больших акушерских синдромов</article-title><trans-title-group xml:lang="en"><trans-title>Transcriptomics of placental tissue: identification of molecular mechanisms and measures for targeted therapy of grate obstetric syndromes</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>Трифонова</surname><given-names>Е. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Trifonova</surname><given-names>E. A.</given-names></name></name-alternatives><email xlink:type="simple">ekaterina.trifonova@medgenetics.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>Марков</surname><given-names>А. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Markov</surname><given-names>A. V.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.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>Степанов</surname><given-names>И. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Stepanov</surname><given-names>I. A.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Ижойкина</surname><given-names>Е. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Ijoykina</surname><given-names>E. V.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Степанов</surname><given-names>В. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Stepanov</surname><given-names>V. A.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Научно-исследовательский институт медицинской генетики, Томский национальный исследовательский медицинский центр Российской академии наук</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Research Institute of Medical Genetics, Tomsk National Research Medical Center, Russian Academy of Sciences</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>ОГАУЗ «Областной перинатальный центр им им. И.Д.Евтушенко»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Tomsk Regional Perinatal Center</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2020</year></pub-date><pub-date pub-type="epub"><day>02</day><month>02</month><year>2021</year></pub-date><volume>19</volume><issue>11</issue><fpage>73</fpage><lpage>75</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Трифонова Е.А., Марков А.В., Степанов И.А., Ижойкина Е.В., Степанов В.А., 2021</copyright-statement><copyright-year>2021</copyright-year><copyright-holder xml:lang="ru">Трифонова Е.А., Марков А.В., Степанов И.А., Ижойкина Е.В., Степанов В.А.</copyright-holder><copyright-holder xml:lang="en">Trifonova E.A., Markov A.V., Stepanov I.A., Ijoykina E.V., Stepanov V.A.</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.medgen-journal.ru/jour/article/view/1804">https://www.medgen-journal.ru/jour/article/view/1804</self-uri><abstract><p>Многочисленными исследованиями показано, что ключевые патогенетические механизмы больших акушерских синдромов (БАС) связаны с нарушением процессов плацентации. В связи с чем, целью нашей работы являлся поиск новых генетических маркеров этих гестационных осложнений на основе интегративного анализа данных, полученных при полногеномном экспрессионном профилировании плацентарной ткани. Нами выявлено 64 гена, транскрипционная активность которых статистически значимо изменяется как минимум при двух заболеваниях группы БАС. Показана значимая роль нарушения межклеточных взаимодействий и регуляции модификации белков в плацентарной ткани при развитии изученных патологических состояний беременности, идентифицированы мастер-регуляторы, рассматриваемые в качестве потенциальных терапевтических мишеней.</p></abstract><trans-abstract xml:lang="en"><p>It is shown that the key pathogenetic mechanisms of grate obstetric syndromes (GOS) are associated with impaired placentation. The aim of the work was to search for new genetic markers of GOS on the basis of integrative analysis of genome-wide expression profiling data. We found that the transcriptional activity of 64 genes changes in at least two GOS diseases. The significant role of disturbance of intercellular interactions and regulation of protein modification in placental tissue during the development of the pregnancy complications is shown. Master regulators that are potential therapeutic targets have been identified.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>транскриптом</kwd><kwd>плацента</kwd><kwd>мастер-регулятор</kwd><kwd>большие акушерские синдромы</kwd></kwd-group><kwd-group xml:lang="en"><kwd>transcriptome</kwd><kwd>placenta</kwd><kwd>master regulator</kwd><kwd>grate obstetric syndromes</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">Trifonova E.A., Gabidulina T.V., Ershov N.I., Serebrova V.N., Vorozhishcheva A.Y., Stepanov V.A. Analysis of the placental tissue transcriptome of normal and preeclampsia complicated pregnancies. Acta Naturae. 2014;6(2):71-83.</mixed-citation><mixed-citation xml:lang="en">Trifonova E.A., Gabidulina T.V., Ershov N.I., Serebrova V.N., Vorozhishcheva A.Y., Stepanov V.A. Analysis of the placental tissue transcriptome of normal and preeclampsia complicated pregnancies. Acta Naturae. 2014;6(2):71-83.</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>
