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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">mimmun</journal-id><journal-title-group><journal-title xml:lang="ru">Медицинская иммунология</journal-title><trans-title-group xml:lang="en"><trans-title>Medical Immunology (Russia)</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1563-0625</issn><issn pub-type="epub">2313-741X</issn><publisher><publisher-name>SPb RAACI</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.15789/1563-0625-2017-2-185-190</article-id><article-id custom-type="elpub" pub-id-type="custom">mimmun-1221</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>SHORT COMMUNICATIONS</subject></subj-group></article-categories><title-group><article-title>ПОЛИМОРФИЗМ ПРОМОТОРОВ ГЕНОВ РЕЦЕПТОРОВ ФАКТОРА НЕКРОЗА ОПУХОЛИ И ИНТЕРЛЕЙКИНА-1 У БОЛЬНЫХ РАКОМ МОЛОЧНОЙ ЖЕЛЕЗЫ</article-title><trans-title-group xml:lang="en"><trans-title>PROMOTER POLYMORPHISMS OF GENES ENCODING TUMOR NECROSIS FACTOR AND INTERLEUKIN-1 IN BREAST CANCER PATIENTS</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>Силков</surname><given-names>А. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Silkov</surname><given-names>A. N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>ведущий научный сотрудник лаборатории молекулярной иммунологии</p></bio><bio xml:lang="en"><p>PhD, MD (Biology), Leading Research Associate, Laboratory of Molecular Immunology</p></bio><email xlink:type="simple">sennikovsv@gmail.com</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>Чердынцева</surname><given-names>Н. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Cherdyntseva</surname><given-names>N. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>д.б.н., профессор, заместитель директора по научной работе</p></bio><bio xml:lang="en"><p>PhD, MD (Biology), Professor, Deputy Director</p></bio><email xlink:type="simple">sennikovsv@gmail.com</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>Максимов</surname><given-names>В. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Maximov</surname><given-names>V. N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>д.м.н., заведующий лабораторией молекулярно-генетических исследований терапевтических заболеваний</p></bio><bio xml:lang="en"><p>PhD, MD (Medicine), Head, Laboratory of Molecular Genetics Studies of Therapeutic Diseases</p></bio><email xlink:type="simple">sennikovsv@gmail.com</email><xref ref-type="aff" rid="aff-3"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Сенников</surname><given-names>С. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Sennikov</surname><given-names>S. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>д.м.н., профессор, заведующий лабораторией молекулярной иммунологии</p></bio><bio xml:lang="en"><p>PhD, MD (Medicine), Professor, Head Laboratory of Molecular Immunology</p></bio><email xlink:type="simple">sennikovsv@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФГБНУ «Научно-исследовательский институт фундаментальной и клинической иммунологии», г. Новосибирск</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Research Institute of Fundamental and Clinical Immunology, Novosibirsk</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>ФГБНУ «Томский национальный исследовательский медицинский центр Российской академии наук», г. Томск</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Tomsk National Research Medical Center, Russian Academy of Sciences, Tomsk</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-3"><aff xml:lang="ru"><institution>ФГБНУ «Научно-исследовательский институт терапии и профилактической медицины», г. Новосибирск</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Research Institute of Therapy and Preventive Medicine, Novosibirsk</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2017</year></pub-date><pub-date pub-type="epub"><day>06</day><month>05</month><year>2017</year></pub-date><volume>19</volume><issue>2</issue><fpage>185</fpage><lpage>190</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Силков А.Н., Чердынцева Н.В., Максимов В.Н., Сенников С.В., 2017</copyright-statement><copyright-year>2017</copyright-year><copyright-holder xml:lang="ru">Силков А.Н., Чердынцева Н.В., Максимов В.Н., Сенников С.В.</copyright-holder><copyright-holder xml:lang="en">Silkov A.N., Cherdyntseva N.V., Maximov V.N., Sennikov S.V.</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.mimmun.ru/mimmun/article/view/1221">https://www.mimmun.ru/mimmun/article/view/1221</self-uri><abstract><sec><title>Резюме</title><p>Резюме. Поиск молекулярно-генетических маркеров риска и прогноза рака молочной железы является одним из актуальных направлений современных исследований. Множество молекулярных механизмов, вовлеченных в патогенез рака молочной железы, определяет широкий спектр возможных генов-кандидатов. Одними из потенциальных кандидатов являются гены рецепторов провоспалительных цитокинов, например фактора некроза опухолей и интерлейкина-1. Для них показано наличие функциональных аллельных вариантов, ассоциированных с изменением уровня экспрессии растворимых и мембраносвязанных форм рецепторов. Кроме того, они представлены как на иммунокомпетентных клетках, так и на клетках эпителия и эндотелия и регулируют функциональное состояние клеток, активность синтеза ферментов межклеточного матрикса и факторов ангиогнеза, что и определяет вклад этих рецепторных белков в патогенез опухолевого роста. Целью настоящего исследования был сравнительный анализ частот аллельных вариантов генов рецепторов TNF и IL-1 у больных раком молочной железы и здоровых женщин. Проведено генотипирование полиморфизмов rs4149569 TNFRSF1A, rs590368 TNFRSF1B, rs2234650 IL1RI и rs4141134 IL1R2, для которых ранее была установлена ассоциация с уровнем экспрессии рецепторов TNF и IL-1 на иммунокомпетентных клетках. Сравнительный анализ частот генотипов в исследованных выборках показал значимое снижение частоты гомозигот СС полиморфизма rs590368 гена TNFRSF1B и увеличение числа гетерозигот СТ полиморфизма rs2234650 гена IL1R1 в выборке больных раком молочной железы. Генетический полиморфизм, ассоциированный с уровнем экспрессии рецепторов TNF и IL-1 на иммунокомпетентных клетках, может являться одним из факторов, регулирующих участие провоспалительных цитокинов в иммунопатогенезе рака молочной железы.</p></sec><sec><title> </title><p> </p></sec></abstract><trans-abstract xml:lang="en"><p>Search for molecular genetic markers of risk and prognosis of breast cancer is an important prospective of modern research. Many molecular mechanisms are involved in pathogenesis of breast cancer and define a wide range of possible candidate genes. The genes of pro-inflammatory cytokine receptors, such as tumor necrosis factor and interleukin-1, are also among potential candidate genes. Numerous functional allelic variants of these genes have been shown which are associated with changed expression of membranebound and soluble forms of the receptors. In addition, they are expressed both on immunе cells and epithelial and endothelial cells. They regulate functional status of the cells, synthesis and activities of enzymes controlling extracellular matrix and angiogenesis factors. These functions of tumor necrosis factor and interleukin-1 receptor proteins may contribute to pathogenesis of tumor growth. The aim of present study was to compare frequency of functional allelic variants of genes encoding TNF and IL-1 receptors in breast cancer patients and healthy women. We performed genotyping of distinct SNPs (rs4149569 TNFRSF1A, rs590368 TNFRSF1B, rs2234650 IL1RI, and rs4141134 IL1R2) that previously were shown to be associated with expression of TNF and IL-1 receptors on immune cells. Comparative analysis of the genotype frequencies in the samples under study showed a significantly reduced frequency of CC homozygotes for rs590368 polymorphism (TNFRSF1B gene), and increased ratio of CT heterozygotes for rs2234650 polymorphism (IL1R1 gene) among breast cancer patients. Hence, some gene polymorphisms associated with altered expression levels of TNF and IL-1 receptors on immune cells may represent a factor which may determine involvement of proinflammatory cytokines into pathogenesis of breast cancer.</p><p> </p></trans-abstract><kwd-group xml:lang="ru"><kwd>рецепторы цитокинов</kwd><kwd>генетический полиморфизм</kwd><kwd>TNFRSF1A</kwd><kwd>TNFRSF1B</kwd><kwd>IL1RI</kwd><kwd>IL1RII</kwd><kwd>рак молочной железы</kwd></kwd-group><kwd-group xml:lang="en"><kwd>cytokine receptors</kwd><kwd>gene polymorphism</kwd><kwd>TNFRSF1A</kwd><kwd>TNFRSF1B</kwd><kwd>IL1RI</kwd><kwd>IL1RII</kwd><kwd>breast cancer</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">Каприн А.Д., Старинский В.В., Петров Г.В. Состояние онкологической помощи населению России в 2013 году. М.: ФГБУ «МНИОИ им. П.А. Герцена» Минздрава России, 2014. 235 c. 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