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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">ssmu</journal-id><journal-title-group><journal-title xml:lang="ru">Бюллетень сибирской медицины</journal-title><trans-title-group xml:lang="en"><trans-title>Bulletin of Siberian Medicine</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1682-0363</issn><issn pub-type="epub">1819-3684</issn><publisher><publisher-name>Siberian State Medical University, the Ministry of Healthcare of the Russian Federation</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.20538/1682-0363-2018-3-61-69</article-id><article-id custom-type="elpub" pub-id-type="custom">ssmu-1284</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>ОРИГИНАЛЬНЫЕ СТАТЬИ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>ORIGINAL PAPERS</subject></subj-group></article-categories><title-group><article-title>Новые кандидатные маркеры плоскоклеточного рака головы и шеи</article-title><trans-title-group xml:lang="en"><trans-title>Molecular features of head and neck squamous cell carcinoma</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-4506-9429</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Какурина</surname><given-names>Г. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Kakurina</surname><given-names>G. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Какурина Гелена Валерьевна - кандидат медицинских наук, старший научный сотрудник, лаборатория биохимии опухолей.</p><p>634050, Томск, пер. Кооперативный, 2</p></bio><bio xml:lang="en"><p>Kakurina Gelena V. - PhD, Senior Researcher, Laboratory of Tumor Biochemistry.</p><p>5, Kooperativny Str., Tomsk, 634050</p></bio><email xlink:type="simple">kakurinagv@oncology.tomsk.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/0000-0001-9122-3274</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Колегова</surname><given-names>Е. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Kolegova</surname><given-names>E. S.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Колегова Елена Сергеевна - младший научный сотрудник, лаборатория биохимии опухолей,  НИИ онкологии, ТНИМЦ РАН.</p><p>634050, Томск, пер. Кооперативный, 2; 634050, Томск, Московский тракт, 2; 89234407523</p></bio><bio xml:lang="en"><p>Kolegova Elena S. - Junior Researcher, Laboratory of Tumor Biochemistry, Cancer Research Institute, TNRMC RAS.</p><p>5, Kooperativny Str., Tomsk, 634050; 2, Moscow Trakt, Tomsk, 634050</p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-7234-4708</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Черемисина</surname><given-names>О. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Cheremisina</surname><given-names>О. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Черемисина Ольга Владимировна - докторр медицинских наук, зав. ýндоскопическим отделением, НИИ онкологии, ТНИМЦ РАН.</p><p>634050, Томск, пер. Кооперативный, 2</p></bio><bio xml:lang="en"><p>Cheremisina Оlga V. - DM, Head of the Endoscopy Department.</p><p>5, Kooperativny Str., Tomsk, 634050</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-3651-0665</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Чойнзонов</surname><given-names>Е. Л.</given-names></name><name name-style="western" xml:lang="en"><surname>Choinzonov</surname><given-names>Е. L.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Чойнзонов Евгений Лхамацыренович - докторр медицинских наук, профессор, академик РАН,  директор НИИ онкологии, ТНИМЦ РАН; заведующий кафедрой онкологии, СибГМУ.</p><p>634050, Томск, пер. Кооперативный, 2; 634050, Томск, Московский тракт, 2</p></bio><bio xml:lang="en"><p>Choinzonov Еvgeny L. - DM, Professor, Academician of RAS, Director of TNRMC, Cancer Research Institute, TNRMC RAS; SSMU.</p><p>5, Kooperativny Str., Tomsk, 634050; 2, Moscow Trakt, Tomsk, 634050</p></bio><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Научно-исследовательский институт (НИИ) онкологии, Томский национальный исследовательский  медицинский центр (ТНИМЦ) Российской академии наук (РАН)</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Cancer Research Institute, Tomsk National Research Medical Center (TNRМС) of Russian Academy of Science (RAS)</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Научно-исследовательский институт (НИИ) онкологии, Томский национальный исследовательский  медицинский центр (ТНИМЦ) Российской академии наук (РАН); Сибирский государственный медицинский университет (СибГМУ)</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Cancer Research Institute, Tomsk National Research Medical Center (TNRМС) of Russian Academy of Science (RAS); Siberian State Medical University (SSMU)</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2018</year></pub-date><pub-date pub-type="epub"><day>29</day><month>09</month><year>2018</year></pub-date><volume>17</volume><issue>3</issue><fpage>61</fpage><lpage>69</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Какурина Г.В., Колегова Е.С., Черемисина О.В., Чойнзонов Е.Л., 2018</copyright-statement><copyright-year>2018</copyright-year><copyright-holder xml:lang="ru">Какурина Г.В., Колегова Е.С., Черемисина О.В., Чойнзонов Е.Л.</copyright-holder><copyright-holder xml:lang="en">Kakurina G.V., Kolegova E.S., Cheremisina О.V., Choinzonov Е.L.</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://bulletin.ssmu.ru/jour/article/view/1284">https://bulletin.ssmu.ru/jour/article/view/1284</self-uri><abstract><sec><title>Актуальность</title><p>Актуальность. Для выявления новых маркеров ранней диагностики и прогноза течения плоскоклеточного рака головы и шеи (ПРГШ) необходимо изучение молекулярных особенностей этого заболевания. Цель исследования. Сравнительный анализ протеома сыворотки крови больных ПРГШ и здоровых волонтеров, выбор и оценка возможности использования выбранных маркеров для ранней диагностики ПРГШ.</p></sec><sec><title>Материалы и методы</title><p>Материалы и методы. Протеомный анализ сыворотки крови первичных больных ПРГШ с лимфогенными метастазами, без метастазов и здоровых лиц проводили на масс-спектрометре UltraFlexIII TOF/TOF (Bruker, США). Валидация результатов проводилась методом иммуноферментного анализа в сыворотке крови 52 первичных больных ПРГШ (T1-4N0-3M0), 10 пациентов с хроническими гиперпластическими заболеваниями гортани (ХГЗГ) с дисплазией эпителия II−III степени и 10 здоровых лиц. Статистическую обработку проводили с помощью программ Statistica 6.0</p></sec><sec><title>Результаты</title><p>Результаты. Протеом сыворотки крови больных ПРГШ с метастазами, без метастазов и здоровых лиц различен и содержит белки разных классов. Для САР1 был выше, чем полученных результатов выбраны САР1 и у пациентов с ХГЗГ и здоровых лиц почти в два раза (р ≤ 0,05). Уровень сывороточного валидации РРМ1В. Показано, что сывороточный уровень САР1 и РРМ1В различался в группах контроль − ХГЗГ, ХГЗГ − рак (р ≤ 0,05). У больных ПРГШ (T1-N0-M0) уровень сывороточного РРМ1В у больных ХГЗГ и ПРГШ (T1-N0-M0) также был выше контрольного (р ≤ 0,05) и сохранял тенденцию к росту с увеличением стадии. Отмечена положительная связь уровня САР1 в сыворотке крови с наличием метастазов и уровнем РРМ1В.</p></sec></abstract><trans-abstract xml:lang="en"><sec><title>Relevance</title><p>Relevance. To identify new markers of early diagnosis and prognosis of head and neck squamous cell carcinoma (HNSCC) it is necessary to study the molecular features of this disease.</p></sec><sec><title>Purpose</title><p>Purpose. The aim of the study was to analyze blood serum protein spectrum in patients with HNSCC and in healthy volunteers using the methods of mass spectrometry and to evaluate the selected serum protein markers as candidates for early detection of HNSCC.</p></sec><sec><title>Materials and Methods</title><p>Materials and Methods: The blood serum of HNSCC patients before therapy with metastases, without metastases and healthy volunteers was studied by proteomic methods. Validation of the results of proteomic analysis was carried out by ELISA in serum of 52 patients with HNSCC (T1-4N0-3M0), 10 patients with chronic hyperplastic laryngitis, dysplasia DII-DIII and 10 healthy volunteers. The statistical analysis was carried out using Statistica 6.0. Software package.</p></sec><sec><title>Results</title><p>Results. Blood serum proteome of HNSCC patients with metastases, without metastases and healthy volunteers are different and contain proteins of different classes. Adenylyl cyclase-associated protein 1 (CAP1) and protein phosphatase 1B (PPM1B) were selected to validate the obtained results. It was shown that the serum level of CAP1 and PPM1B differed in control and dysplasia groups and dysplasia and cancer groups (p ≤ 0,05). In patients with HNSCC (T1N0M0) the serum CAP1 and PPM1B levels were higher than in patients with dysplasia and healthy individuals (p ≤ 0,05). It was noted the positive correlation of the CAP1 level in the serum with the presence of metastases and the PPM1B level.</p></sec><sec><title>Conclusion</title><p>Conclusion. Candidates for serum markers of HNSCC prognosis were identified. The difference in serum levels of CAP1 and PPM1B depending on the prevalence of primary tumors and the difference in serum level of CAP1 depending on the presence of regional metastases was shown. Determination of CAP1 level in the serum can be useful for early diagnosis and prognosis of HNSCC.</p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>плоскоклеточный рак головы и шеи</kwd><kwd>ранняя диагностика</kwd><kwd>прогноз</kwd><kwd>хронические гиперпластические заболевания гортани</kwd><kwd>дисплазия эпителия</kwd><kwd>протеинфосфатаза 1В</kwd><kwd>аденилил циклаза-ассоциированный протеин 1</kwd></kwd-group><kwd-group xml:lang="en"><kwd>chronic hyperplastic laryngitis and pharyngitis</kwd><kwd>epithelial dysplasia</kwd><kwd>squamous cell carcinoma of head and neck</kwd><kwd>adenylyl cyclase-associated protein 1</kwd><kwd>рrotein phosphatase 1B</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">Плоскоклеточный рак головы и шеи: молекулярные основы патогенеза. 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