<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.3 20210610//EN" "JATS-journalpublishing1-3.dtd">
<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">nogr</journal-id><journal-title-group><journal-title xml:lang="ru">Экспериментальная и клиническая гастроэнтерология</journal-title><trans-title-group xml:lang="en"><trans-title>Experimental and Clinical Gastroenterology</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1682-8658</issn><publisher><publisher-name>«Global Media Technologies»</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.31146/1682-8658-ecg-205-9-190-195</article-id><article-id custom-type="elpub" pub-id-type="custom">nogr-2056</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>ОБЗОР</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>REVIEW</subject></subj-group></article-categories><title-group><article-title>Дисплазии соединительной ткани: онконастороженность</article-title><trans-title-group xml:lang="en"><trans-title>Connective tissue dysplasia: cancer circumspection</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-0601-7044</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Логинова</surname><given-names>Екатерина Николаевна</given-names></name><name name-style="western" xml:lang="en"><surname>Loginova</surname><given-names>E. N.</given-names></name></name-alternatives><email xlink:type="simple">ekaterina.n.loginova@yandex.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>Кирх</surname><given-names>Елизавета Александровна</given-names></name><name name-style="western" xml:lang="en"><surname>Kirkh</surname><given-names>E. A.</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"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-2255-128X</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Нечаева</surname><given-names>Галина Ивановна</given-names></name><name name-style="western" xml:lang="en"><surname>Nechaeva</surname><given-names>G. I.</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"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-4878-0838</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Лялюкова</surname><given-names>Елена Александровна</given-names></name><name name-style="western" xml:lang="en"><surname>Lyalyukova</surname><given-names>E. A.</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"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-6585-131X</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Темерева</surname><given-names>Е. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Temereva</surname><given-names>E. A.</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"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-4016-2023</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Богатырев</surname><given-names>И. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Bogatyrev</surname><given-names>I. 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"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-1375-017X</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Семенова</surname><given-names>Е. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Semenova</surname><given-names>E. V.</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>Федеральное государственное бюджетное образовательное учреждение высшего образования «Омский государственный медицинский университет» Министерства здравоохранения Российской Федерации</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Omsk State Medical University</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2022</year></pub-date><pub-date pub-type="epub"><day>07</day><month>10</month><year>2022</year></pub-date><volume>0</volume><issue>9</issue><fpage>190</fpage><lpage>195</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Логинова Е.Н., Кирх Е.А., Нечаева Г.И., Лялюкова Е.А., Темерева Е.А., Богатырев И.В., Семенова Е.В., 2022</copyright-statement><copyright-year>2022</copyright-year><copyright-holder xml:lang="ru">Логинова Е.Н., Кирх Е.А., Нечаева Г.И., Лялюкова Е.А., Темерева Е.А., Богатырев И.В., Семенова Е.В.</copyright-holder><copyright-holder xml:lang="en">Loginova E.N., Kirkh E.A., Nechaeva G.I., Lyalyukova E.A., Temereva E.A., Bogatyrev I.V., Semenova E.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.nogr.org/jour/article/view/2056">https://www.nogr.org/jour/article/view/2056</self-uri><abstract><p>Особое внимание исследователей во всем мире привлекает патология, обусловленная дисплазиями соединительной ткани, в клинической картине которых ведущими являются кардио-гемодинамические синдромы, невоспалительные структурные сердечно-сосудистые заболевания (расширение корня аорты, пролапсы клапанов сердца и др.). Между тем, в настоящее время появляются данные, свидетельствующие о необходимости онконастороженности у этой когорты пациентов в связи с повышенным риском развития новообразований. Ведущую роль в развитии раковых и предраковых изменений принадлежит трансформирующему фактору роста-β, который может выступать в качестве протоонкогена у пациентов с синдромными формами дисплазий соединительной ткани. При недифференцированых дисплазиях соединительной ткани также отмечен риск развития новообразований различных локализаций. Цель настоящего обзора - систематизация данных, позволяющих оценить - подвержены ли пациенты с дисплазиями соединительной ткани повышенному риску злокачественных новообразований или нет. Коллективом авторов проведен анализ 57 отечественных и зарубежных публикаций, посвященных изучению распространенности и клиническим особенностям злокачественных новообразований у пациентов с дисплазиями соединительной ткани. Обобщение и систематизация современных данных свидетельствуют о том, что пациенты с наследственными нарушениями и недифференцированными дисплазиями соединительной ткани имеют повышенный риск развития опухолей различных локализаций с чертами малигнизации, в том числе вследствие активации сигнального пути трансформирующего фактора роста-β. В связи с этим, активное выявление врачами-специалистами фенотипических признаков наследственных нарушений соединительной ткани и недифференцированных дисплазий соединительной ткани, а также осведомленность о риске развития новообразований у этой когорты пациентов, будет способствовать онконастороженности и проведению активных мероприятий по канцерпревенции.</p></abstract><trans-abstract xml:lang="en"><p>The connective tissue dysplasia attracts the attention of researchers all around the world. Cardio-hemodynamic syndromes, non-inflammatory structural cardiovascular diseases (extension of the aortic root, prolapse of heart valves, etc.) play the leading role in the clinical picture of connective tissue dysplasia. Meanwhile, the cancer circumspection is necessary as well in this cohort of patients due to an increased risk of malignancies. The leading role in the development of cancerous and precancerous changes belongs to the transforming growth factor-β, which can act as a proto-oncogene in patients with syndromic forms of connective tissue dysplasia. In undifferentiated connective tissue dysplasia, there is also a risk of malignancies of various localizations. The aim of this review is to systematize data to assess whether patients with connective tissue dysplasia are at increased risk of malignancies or not. The team of authors analyzed 57 domestic and foreign publications devoted to the study of the prevalence and clinical features of malignancies in patients with connective tissue dysplasia. Systematization of current data suggests that patients with hereditary disorders and undifferentiated connective tissue dysplasia have an increased risk of malignancies of various localizations, including due to dysregulation of TGF-β in various mechanisms of the pathogenesis of connective tissue dysplasia. In this regard, the active identification by medical specialists of the phenotypic signs of hereditary connective tissue disorders and undifferentiated connective tissue dysplasia and awareness of the risk of malignancies developing in this cohort of patients will contribute to cancer circumspection and the implementation of active measures for cancer prevention.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>недифференцированные дисплазии соединительной ткани</kwd><kwd>синдром Марфана</kwd><kwd>онконастороженность</kwd><kwd>трансформирующий фактор роста-β</kwd></kwd-group><kwd-group xml:lang="en"><kwd>undifferentiated connective tissue dysplasia</kwd><kwd>Marfan’s syndrome</kwd><kwd>cancer circumspection</kwd><kwd>transforming growth factor-β</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">Nechaeva G.I., Martynov A. I. Connective tissue dysplasia: cardiovascular changes, modern approaches to diagnosis and treatment. Moscow. LLC “Publishing House “Medical Information Agency”. 2017; 400 p. (In Russ.) @@Нечаева Г. И., Мартынов А. И. Дисплазия соединительной ткани: сердечно-сосудистые изменения, современные подходы к диагностике и лечению. - Москва: ООО «Издательство «Медицинское информационное агентство». 2017; 400 c.</mixed-citation><mixed-citation xml:lang="en">Nechaeva G.I., Martynov A. I. Connective tissue dysplasia: cardiovascular changes, modern approaches to diagnosis and treatment. Moscow. LLC “Publishing House “Medical Information Agency”. 2017; 400 p. (In Russ.) @@Нечаева Г. И., Мартынов А. И. Дисплазия соединительной ткани: сердечно-сосудистые изменения, современные подходы к диагностике и лечению. - Москва: ООО «Издательство «Медицинское информационное агентство». 2017; 400 c.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">National recommendations of the Russian Scientific Medical Society of Therapists on the diagnosis, treatment and rehabilitation of patients with connective tissue dysplasia. Medical Bulletin of the North Caucasus. 2016; 11(1): 2-76. (In Russ.) doi:10.14300/mnnc.2016.11001 @@Национальные рекомендации российского научного медицинского общества терапевтов по диагностике, лечению и реабилитации пациентов с дисплазиями соединительной ткани. Медицинский вестник Северного Кавказа. 2016; 11(1): 2-76. doi:10.14300/mnnc.2016.11001</mixed-citation><mixed-citation xml:lang="en">National recommendations of the Russian Scientific Medical Society of Therapists on the diagnosis, treatment and rehabilitation of patients with connective tissue dysplasia. Medical Bulletin of the North Caucasus. 2016; 11(1): 2-76. (In Russ.) doi:10.14300/mnnc.2016.11001 @@Национальные рекомендации российского научного медицинского общества терапевтов по диагностике, лечению и реабилитации пациентов с дисплазиями соединительной ткани. Медицинский вестник Северного Кавказа. 2016; 11(1): 2-76. doi:10.14300/mnnc.2016.11001</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Hereditary disorders of connective tissue in cardiology. Diagnostics and treatment.Russian Journal of Cardiology. 2013; (1s1):5-32. (In Russ.) doi:10.15829/1560-4071-2013-1s1-5-32 @@Наследственные нарушения соединительной ткани в кардиологии. Диагностика и лечение. Российский кардиологический журнал. 2013; (1s1):5-32. doi:10.15829/1560-4071-2013-1s1-5-32</mixed-citation><mixed-citation xml:lang="en">Hereditary disorders of connective tissue in cardiology. Diagnostics and treatment.Russian Journal of Cardiology. 2013; (1s1):5-32. (In Russ.) doi:10.15829/1560-4071-2013-1s1-5-32 @@Наследственные нарушения соединительной ткани в кардиологии. Диагностика и лечение. Российский кардиологический журнал. 2013; (1s1):5-32. doi:10.15829/1560-4071-2013-1s1-5-32</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Undifferentiated connective tissue dysplasia (draft clinical guidelines). Therapy. 2019; 7:9-42 (In Russ.) doi:10.18565/therapy.2019.7.9-42 @@Недифференцированные дисплазии соединительной ткани (проект клинических рекомендаций). Терапия. 2019; 7:9-42. doi:10.18565/therapy.2019.7.9-42</mixed-citation><mixed-citation xml:lang="en">Undifferentiated connective tissue dysplasia (draft clinical guidelines). Therapy. 2019; 7:9-42 (In Russ.) doi:10.18565/therapy.2019.7.9-42 @@Недифференцированные дисплазии соединительной ткани (проект клинических рекомендаций). Терапия. 2019; 7:9-42. doi:10.18565/therapy.2019.7.9-42</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Hsu C-W., Wang J-C., Liao W-I., et al. Association between malignancies and Marfan syndrome: a population-based, nested case-control study in Taiwan. BMJ Open. 2017; 7: e017243. doi:10.1136/bmjopen-2017-017243</mixed-citation><mixed-citation xml:lang="en">Hsu C-W., Wang J-C., Liao W-I., et al. Association between malignancies and Marfan syndrome: a population-based, nested case-control study in Taiwan. BMJ Open. 2017; 7: e017243. doi:10.1136/bmjopen-2017-017243</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Rudoj A. S., Moskalev A. V., Sbojchakov V. B. The role of transforming growth factor β in the immunopathogenesis of connective tissue diseases. Clinical laboratory diagnostics. 2016;(2): 103-106. (In Russ.) @@Рудой А. С., Москалев А. В., Сбойчаков В. Б. Роль трансформирующего ростового фактора β в иммунопатогенезе заболеваний соединительной ткани. Клиническая лабораторная диагностика. 2016; 2:103-106.</mixed-citation><mixed-citation xml:lang="en">Rudoj A. S., Moskalev A. V., Sbojchakov V. B. The role of transforming growth factor β in the immunopathogenesis of connective tissue diseases. Clinical laboratory diagnostics. 2016;(2): 103-106. (In Russ.) @@Рудой А. С., Москалев А. В., Сбойчаков В. Б. Роль трансформирующего ростового фактора β в иммунопатогенезе заболеваний соединительной ткани. Клиническая лабораторная диагностика. 2016; 2:103-106.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Cherkasov N. S., Lucenko L. A., Ledyaev M. Y. A modern problems of pathogenesis of connective tissue dysplasia in children. Bulletin of VolgSMU. 2020; 4 (76): 16-23. (In Russ.) doi:10.19163/1994-9480-2020-4 (76)-16-23 @@Черкасов Н. С., Луценко Л. А., Ледяев М. Я. Современные проблемы патогенеза дисплазии соединительной ткани у детей. Вестник ВолгГМУ. 2020; 4 (76): 16-23. doi:10.19163/1994-9480-2020-4 (76)-16-23</mixed-citation><mixed-citation xml:lang="en">Cherkasov N. S., Lucenko L. A., Ledyaev M. Y. A modern problems of pathogenesis of connective tissue dysplasia in children. Bulletin of VolgSMU. 2020; 4 (76): 16-23. (In Russ.) doi:10.19163/1994-9480-2020-4 (76)-16-23 @@Черкасов Н. С., Луценко Л. А., Ледяев М. Я. Современные проблемы патогенеза дисплазии соединительной ткани у детей. Вестник ВолгГМУ. 2020; 4 (76): 16-23. doi:10.19163/1994-9480-2020-4 (76)-16-23</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Morikawa M., Derynck R., Miyazono K. TGF-β and the TGF-β Family: Context-Dependent Roles in Cell and Tissue Physiology. Cold Spring Harb Perspect Biol. 2016; 8(5): a021873. doi:10.1086/596254</mixed-citation><mixed-citation xml:lang="en">Morikawa M., Derynck R., Miyazono K. TGF-β and the TGF-β Family: Context-Dependent Roles in Cell and Tissue Physiology. Cold Spring Harb Perspect Biol. 2016; 8(5): a021873. doi:10.1086/596254</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Rudoj A. S. TGF-beta-dependent pathogenesis of Marfan syndrome and related hereditary connective tissue disorders. Arterial hypertension. 2009; 15(2):223-226. (In Russ.) @@Рудой А. С. TGF-beta-зависимый патогенез синдрома Марфана и родственных наследственных нарушений соединительной ткани. Артериальная гипертензия. 2009; 15(2):223-226.</mixed-citation><mixed-citation xml:lang="en">Rudoj A. S. TGF-beta-dependent pathogenesis of Marfan syndrome and related hereditary connective tissue disorders. Arterial hypertension. 2009; 15(2):223-226. (In Russ.) @@Рудой А. С. TGF-beta-зависимый патогенез синдрома Марфана и родственных наследственных нарушений соединительной ткани. Артериальная гипертензия. 2009; 15(2):223-226.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Torshin I.YU., Gromova O. A. Connective tissue dysplasia, cellular biology and molecular mechanisms of magnesium exposure.Rus. med. journal: selected lectures for family doctors. 2008; 16 (4): 8-12. (In Russ.) @@Торшин И. Ю., Громова О. А. Дисплазия соединительной ткани, клеточная биология и молекулярные механизмы воздействия магния. Рус. мед. журнал: избранные лекции для семейных врачей. 2008; 16 (4): 8-12.</mixed-citation><mixed-citation xml:lang="en">Torshin I.YU., Gromova O. A. Connective tissue dysplasia, cellular biology and molecular mechanisms of magnesium exposure.Rus. med. journal: selected lectures for family doctors. 2008; 16 (4): 8-12. (In Russ.) @@Торшин И. Ю., Громова О. А. Дисплазия соединительной ткани, клеточная биология и молекулярные механизмы воздействия магния. Рус. мед. журнал: избранные лекции для семейных врачей. 2008; 16 (4): 8-12.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Kryganova T. A. Specific features of urinary system diseases in children with connective tissue dysplasia.Russian Bulletin of Perinatology and Pediatrics. 2015;60(6):33-37. (In Russ.) @@Крыганова Т. А. Особенности заболеваний органов мочевой системы у детей с дисплазиями соединительной ткани. Российский вестник перинатологии и педиатрии. 2015;60(6):33-37.</mixed-citation><mixed-citation xml:lang="en">Kryganova T. A. Specific features of urinary system diseases in children with connective tissue dysplasia.Russian Bulletin of Perinatology and Pediatrics. 2015;60(6):33-37. (In Russ.) @@Крыганова Т. А. Особенности заболеваний органов мочевой системы у детей с дисплазиями соединительной ткани. Российский вестник перинатологии и педиатрии. 2015;60(6):33-37.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Halushka M. K., Angelini A., Bartoloni G., et al. Consensus statement on surgical pathology of the aorta from the Society for Cardiovascular Pathology and the Association For European Cardiovascular Pathology: II. Noninflammatory degenerative diseases - nomenclature and diagnostic criteria. Cardiovasc Pathol. 2016; 25 (3), 247-57. doi:10.1016/j.carpath.2016.03.002</mixed-citation><mixed-citation xml:lang="en">Halushka M. K., Angelini A., Bartoloni G., et al. Consensus statement on surgical pathology of the aorta from the Society for Cardiovascular Pathology and the Association For European Cardiovascular Pathology: II. Noninflammatory degenerative diseases - nomenclature and diagnostic criteria. Cardiovasc Pathol. 2016; 25 (3), 247-57. doi:10.1016/j.carpath.2016.03.002</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Cook J. R., Carta L., Galatioto J., et al. Cardiovascular manifestations in Marfan syndrome and related diseases; multiple genes causing similar phenotypes. Clin Genet. 2015; 87:11-20. doi:10.1111/cge.12436</mixed-citation><mixed-citation xml:lang="en">Cook J. R., Carta L., Galatioto J., et al. Cardiovascular manifestations in Marfan syndrome and related diseases; multiple genes causing similar phenotypes. Clin Genet. 2015; 87:11-20. doi:10.1111/cge.12436</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">De Cario R., Sticchi E., Lucarini L., et al. Role of TGFBR1 and TGFBR2 genetic variants in Marfan syndrome. Journal of vascular surgery. 2018; 68(1): 225-233.e5. doi:10.1016/j.jvs.2017.04.071</mixed-citation><mixed-citation xml:lang="en">De Cario R., Sticchi E., Lucarini L., et al. Role of TGFBR1 and TGFBR2 genetic variants in Marfan syndrome. Journal of vascular surgery. 2018; 68(1): 225-233.e5. doi:10.1016/j.jvs.2017.04.071</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Rudoj A. S., Letkovskaya T. A., Uryvaev A. M., et al. The role of TGF-ß induction and gastrointestinal myofibroblasts in the pathomorphogenesis of chronic gastritis in patients with Marfan syndrome and Marfan-like conditions. Experimental and clinical gastroenterology. 2016; (6):14-18. (In Russ.) @@Рудой А. С., Летковская Т. А., Урываев А. М. и др. Роль TGFΒ-индукции и гастроинтестинальных миофибробластов в патоморфогенезе хронического гастрита у пациентов с синдромом Марфана и марфаноподобными состояниями. Экспериментальная и клиническая гастроэнтерология. 2016;(6): 14-18.</mixed-citation><mixed-citation xml:lang="en">Rudoj A. S., Letkovskaya T. A., Uryvaev A. M., et al. The role of TGF-ß induction and gastrointestinal myofibroblasts in the pathomorphogenesis of chronic gastritis in patients with Marfan syndrome and Marfan-like conditions. Experimental and clinical gastroenterology. 2016; (6):14-18. (In Russ.) @@Рудой А. С., Летковская Т. А., Урываев А. М. и др. Роль TGFΒ-индукции и гастроинтестинальных миофибробластов в патоморфогенезе хронического гастрита у пациентов с синдромом Марфана и марфаноподобными состояниями. Экспериментальная и клиническая гастроэнтерология. 2016;(6): 14-18.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Somers A. E., Hinton R. B., Pilipenko V., et al. Analysis of TGFBR1*6A variant in individuals evaluated for Marfan syndrome. American journal of medical genetics. Part A/ 2016; 170(7): 1786-1790. doi:10.1002/ajmg.a.37668</mixed-citation><mixed-citation xml:lang="en">Somers A. E., Hinton R. B., Pilipenko V., et al. Analysis of TGFBR1*6A variant in individuals evaluated for Marfan syndrome. American journal of medical genetics. Part A/ 2016; 170(7): 1786-1790. doi:10.1002/ajmg.a.37668</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Morissette R., Schoenhoff F., Xu Z., et al. Transforming growth factor-β and inflammation in vascular (type IV) Ehlers-Danlos syndrome. Circulation. Cardiovascular genetics. 2014; 7(1): 80-88. doi:10.1161/CIRCGENETICS.113.000280</mixed-citation><mixed-citation xml:lang="en">Morissette R., Schoenhoff F., Xu Z., et al. Transforming growth factor-β and inflammation in vascular (type IV) Ehlers-Danlos syndrome. Circulation. Cardiovascular genetics. 2014; 7(1): 80-88. doi:10.1161/CIRCGENETICS.113.000280</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Franken R., den Hartog A. W., de Waard V., et al. Circulating transforming growth factor-β as a prognostic biomarker in Marfan syndrome.International journal of cardiology. 2013; 168(3)2441-2446. Doi: 10.1016/j.ijcard.2013.03.033</mixed-citation><mixed-citation xml:lang="en">Franken R., den Hartog A. W., de Waard V., et al. Circulating transforming growth factor-β as a prognostic biomarker in Marfan syndrome.International journal of cardiology. 2013; 168(3)2441-2446. Doi: 10.1016/j.ijcard.2013.03.033</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Derynck R., Akhurst R. J., Balmain A. TGF-β signaling in tumor suppression and cancer progression. Nat Genet. 2001; 29: 117-129. doi:10.1038/ng1001-117</mixed-citation><mixed-citation xml:lang="en">Derynck R., Akhurst R. J., Balmain A. TGF-β signaling in tumor suppression and cancer progression. Nat Genet. 2001; 29: 117-129. doi:10.1038/ng1001-117</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Kubiczkova L., Sedlarikova L., Hajek R., et al. TGF-β - an excellent servant but a bad master. J Transl Med. 2012; 10:183. doi:10.1186/1479-5876-10-183</mixed-citation><mixed-citation xml:lang="en">Kubiczkova L., Sedlarikova L., Hajek R., et al. TGF-β - an excellent servant but a bad master. J Transl Med. 2012; 10:183. doi:10.1186/1479-5876-10-183</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Syed V. TGF-β Signaling in Cancer. J Cell Biochem. 2016; 117(6):1279-87. doi:10.1002/jcb.25496</mixed-citation><mixed-citation xml:lang="en">Syed V. TGF-β Signaling in Cancer. J Cell Biochem. 2016; 117(6):1279-87. doi:10.1002/jcb.25496</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Tirado-Rodriguez B., Ortega E., Segura-Medina P., et al. TGF- β: an important mediator of allergic disease and a molecule with dual activity in cancer development. J Immunol Res. 2014; 2014:318481. doi:10.1155/2014/318481</mixed-citation><mixed-citation xml:lang="en">Tirado-Rodriguez B., Ortega E., Segura-Medina P., et al. TGF- β: an important mediator of allergic disease and a molecule with dual activity in cancer development. J Immunol Res. 2014; 2014:318481. doi:10.1155/2014/318481</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Katsuno Y., Lamouille S., Derynck R. TGF-β signaling and epithelial-mesenchymal transition in cancer progression. Current opinion in oncology. 2013; 25(1): 76-84. doi:10.1097/CCO.0b013e32835b6371</mixed-citation><mixed-citation xml:lang="en">Katsuno Y., Lamouille S., Derynck R. TGF-β signaling and epithelial-mesenchymal transition in cancer progression. Current opinion in oncology. 2013; 25(1): 76-84. doi:10.1097/CCO.0b013e32835b6371</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Mizuguchi T., Collod-Beroud G., Akiyama T., et al. Heterozygous TGFBR2 mutations in Marfan syndrome. Nature genetics. 2004; 36(8): 855-860. doi:10.1038/ng1392</mixed-citation><mixed-citation xml:lang="en">Mizuguchi T., Collod-Beroud G., Akiyama T., et al. Heterozygous TGFBR2 mutations in Marfan syndrome. Nature genetics. 2004; 36(8): 855-860. doi:10.1038/ng1392</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Liu J. F., Mao L., Bu L. L., et al. C4.4A as a biomarker of head and neck squamous cell carcinoma and correlated with epithelial mesenchymal transition. Am J Cancer Res. 2015; 5:3505-3515. PMID: 26885441.</mixed-citation><mixed-citation xml:lang="en">Liu J. F., Mao L., Bu L. L., et al. C4.4A as a biomarker of head and neck squamous cell carcinoma and correlated with epithelial mesenchymal transition. Am J Cancer Res. 2015; 5:3505-3515. PMID: 26885441.</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Liang Y., Zhu F., Zhang H., et al. Conditional ablation of TGF-β signaling inhibits tumor progression and invasion in an induced mouse bladder cancer model. Scientific reports. 2016; 6 (29479): 1-8. doi:10.1038/srep29479</mixed-citation><mixed-citation xml:lang="en">Liang Y., Zhu F., Zhang H., et al. Conditional ablation of TGF-β signaling inhibits tumor progression and invasion in an induced mouse bladder cancer model. Scientific reports. 2016; 6 (29479): 1-8. doi:10.1038/srep29479</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Korrodi-Gregório L., Silva J. V., Santos-Sousa L., et al. TGF-β cascade regulation by PPP1 and its interactors -impact on prostate cancer development and therapy. Journal of cellular and molecular medicine. 2014; 18(4): 555-567. doi:10.1111/jcmm.12266</mixed-citation><mixed-citation xml:lang="en">Korrodi-Gregório L., Silva J. V., Santos-Sousa L., et al. TGF-β cascade regulation by PPP1 and its interactors -impact on prostate cancer development and therapy. Journal of cellular and molecular medicine. 2014; 18(4): 555-567. doi:10.1111/jcmm.12266</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Ramamoorthi G., Sivalingam N. Molecular mechanism of TGF-β signaling pathway in colon carcinogenesis and status of curcumin as chemopreventive strategy. Tumor biology: the journal of the International Society for Oncodevelopmental Biology and Medicine. 2014; 35(8):7295-7305. doi:10.1007/s13277-014-1840-1</mixed-citation><mixed-citation xml:lang="en">Ramamoorthi G., Sivalingam N. Molecular mechanism of TGF-β signaling pathway in colon carcinogenesis and status of curcumin as chemopreventive strategy. Tumor biology: the journal of the International Society for Oncodevelopmental Biology and Medicine. 2014; 35(8):7295-7305. doi:10.1007/s13277-014-1840-1</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Jeon H. S., Jen J. TGF-beta signaling and the role of inhibitory Smads in non-small cell lung cancer. Journal of thoracic oncology: official publication of the International Association for the Study of Lung Cancer. 2010; 5(4):417-419. doi:10.1097/JTO.0b013e3181ce3afd</mixed-citation><mixed-citation xml:lang="en">Jeon H. S., Jen J. TGF-beta signaling and the role of inhibitory Smads in non-small cell lung cancer. Journal of thoracic oncology: official publication of the International Association for the Study of Lung Cancer. 2010; 5(4):417-419. doi:10.1097/JTO.0b013e3181ce3afd</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Zarzynska J. M. Two faces of TGF-beta1 in breast cancer. Mediators of inflammation. 2014; 141747:1-16. doi:10.1155/2014/141747</mixed-citation><mixed-citation xml:lang="en">Zarzynska J. M. Two faces of TGF-beta1 in breast cancer. Mediators of inflammation. 2014; 141747:1-16. doi:10.1155/2014/141747</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Yoshida K., Murata M., Yamaguchi T., et al. TGF-β/Smad signaling during hepatic fibro-carcinogenesis (review).International journal of oncology. 2014;45(4): 1363-1371. doi:10.3892/ijo.2014.2552</mixed-citation><mixed-citation xml:lang="en">Yoshida K., Murata M., Yamaguchi T., et al. TGF-β/Smad signaling during hepatic fibro-carcinogenesis (review).International journal of oncology. 2014;45(4): 1363-1371. doi:10.3892/ijo.2014.2552</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Boström A. K., Lindgren D., Johansson M. E., et al. Effects of TGF-β signaling in clear cell renal cell carcinoma cells. Biochemical and biophysical research communications. 2013; 435(1): 126-133. doi:10.1016/j.bbrc.2013.04.054</mixed-citation><mixed-citation xml:lang="en">Boström A. K., Lindgren D., Johansson M. E., et al. Effects of TGF-β signaling in clear cell renal cell carcinoma cells. Biochemical and biophysical research communications. 2013; 435(1): 126-133. doi:10.1016/j.bbrc.2013.04.054</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Sitaram R. T., Mallikarjuna P., Landström M., Ljungberg B. Transforming growth factor-β promotes aggressiveness and invasion of clear cell renal cell carcinoma. Oncotarget. 2016; 14;7(24):35917-35931. doi:10.18632/oncotarget.9177</mixed-citation><mixed-citation xml:lang="en">Sitaram R. T., Mallikarjuna P., Landström M., Ljungberg B. Transforming growth factor-β promotes aggressiveness and invasion of clear cell renal cell carcinoma. Oncotarget. 2016; 14;7(24):35917-35931. doi:10.18632/oncotarget.9177</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Winer D. A., Winer S., Rotstein L., et al. Villous papillary thyroid carcinoma: a variant associated with Marfan syndrome. Endocrine pathology. 2012; 23(4): 254-259. doi:10.1007/s12022-012-9219-6</mixed-citation><mixed-citation xml:lang="en">Winer D. A., Winer S., Rotstein L., et al. Villous papillary thyroid carcinoma: a variant associated with Marfan syndrome. Endocrine pathology. 2012; 23(4): 254-259. doi:10.1007/s12022-012-9219-6</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Roopnariane A., Freed R. J., Price S., et al. Osteosarcoma in a Marfan patient with a novel premature termination codon in the FBN1 gene. Connective tissue research. 2011; 52(2): 157-165. doi:10.3109/03008207.2010.500430</mixed-citation><mixed-citation xml:lang="en">Roopnariane A., Freed R. J., Price S., et al. Osteosarcoma in a Marfan patient with a novel premature termination codon in the FBN1 gene. Connective tissue research. 2011; 52(2): 157-165. doi:10.3109/03008207.2010.500430</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Garcia-Rendueles A.R., Rodrigues J. S., Garcia-Rendueles M. E., et al. Rewiring of the apoptotic TGF-β-SMAD/NFκB pathway through an oncogenic function of p27 in human papillary thyroid cancer. Oncogene. 2017;36(5):652-666. doi:10.1038/onc.2016.233</mixed-citation><mixed-citation xml:lang="en">Garcia-Rendueles A.R., Rodrigues J. S., Garcia-Rendueles M. E., et al. Rewiring of the apoptotic TGF-β-SMAD/NFκB pathway through an oncogenic function of p27 in human papillary thyroid cancer. Oncogene. 2017;36(5):652-666. doi:10.1038/onc.2016.233</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Bisconti M., Bisetti A., Bidoli P. Malignant mesothelioma in subjects with Marfan’s syndrome and Ehlers-Danlos syndrome: only an apparent association? Respiration: international review of thoracic diseases. 2000;67(2): 223-228. doi:10.1159/000029493</mixed-citation><mixed-citation xml:lang="en">Bisconti M., Bisetti A., Bidoli P. Malignant mesothelioma in subjects with Marfan’s syndrome and Ehlers-Danlos syndrome: only an apparent association? Respiration: international review of thoracic diseases. 2000;67(2): 223-228. doi:10.1159/000029493</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Rudoj A. S. Uryvaev A. M. Pathogenetic mechanisms of the development of precancerous changes in the stomach in patients with Marfan syndrome. Terapiya. 2020; 6(40): 71-81. (In Russ.) doi:10.18565/therapy.2020.6.71-81 @@Рудой А. С., Урываев А. М. Патогенетические механизмы развития предраковых изменений желудка у пациентов с синдромом Марфана. Терапия. 2020; 6(40): 71-81. doi:10.18565/therapy.2020.6.71-81</mixed-citation><mixed-citation xml:lang="en">Rudoj A. S. Uryvaev A. M. Pathogenetic mechanisms of the development of precancerous changes in the stomach in patients with Marfan syndrome. Terapiya. 2020; 6(40): 71-81. (In Russ.) doi:10.18565/therapy.2020.6.71-81 @@Рудой А. С., Урываев А. М. Патогенетические механизмы развития предраковых изменений желудка у пациентов с синдромом Марфана. Терапия. 2020; 6(40): 71-81. doi:10.18565/therapy.2020.6.71-81</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Milleron O., Arnoult F., Ropers J., et al. Marfan Sartan: a randomized, double-blind, placebo-controlled trial. European heart journal. 2015; 36(32): 2160-2166. doi:10.1093/eurheartj/ehv151</mixed-citation><mixed-citation xml:lang="en">Milleron O., Arnoult F., Ropers J., et al. Marfan Sartan: a randomized, double-blind, placebo-controlled trial. European heart journal. 2015; 36(32): 2160-2166. doi:10.1093/eurheartj/ehv151</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Okada M., Takeuchi E., Mori Y., et al. An autopsy case of angiosarcoma arising around a woven Dacron prosthesis after a Cabrol operation. The Journal of thoracic and cardiovascular surgery. 2004; 127(6):1843-1845. doi:10.1016/j.jtcvs.2004.01.021</mixed-citation><mixed-citation xml:lang="en">Okada M., Takeuchi E., Mori Y., et al. An autopsy case of angiosarcoma arising around a woven Dacron prosthesis after a Cabrol operation. The Journal of thoracic and cardiovascular surgery. 2004; 127(6):1843-1845. doi:10.1016/j.jtcvs.2004.01.021</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Fassbender W. J., Krohn-Grimberghe B., Görtz B., et al. Multiple endocrine neoplasia (MEN) - an overview and case report - patient with sporadic bilateral pheochromocytoma, hyperparathyroidism and marfanoid habitus. Anticancer research. 2000; 20(6C): 4877-4887. PMID: 11205236.</mixed-citation><mixed-citation xml:lang="en">Fassbender W. J., Krohn-Grimberghe B., Görtz B., et al. Multiple endocrine neoplasia (MEN) - an overview and case report - patient with sporadic bilateral pheochromocytoma, hyperparathyroidism and marfanoid habitus. Anticancer research. 2000; 20(6C): 4877-4887. PMID: 11205236.</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Sotos J. G. Abraham Lincoln’s marfanoid mother: the earliest known case of multiple endocrine neoplasia type 2B? Clinical dysmorphology. 2012; 21(3):131-136. doi:10.1097/MCD.0b013e328353ae0c</mixed-citation><mixed-citation xml:lang="en">Sotos J. G. Abraham Lincoln’s marfanoid mother: the earliest known case of multiple endocrine neoplasia type 2B? Clinical dysmorphology. 2012; 21(3):131-136. doi:10.1097/MCD.0b013e328353ae0c</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Rouce R. H., Shaim H., Sekine T., et al. The TGF-β/SMAD pathway is an important mechanism for NK cell immune evasion in childhood B-acute lymphoblastic leukemia. Leukemia. 2016; 30(4): 800-811. doi:10.1038/leu.2015.327</mixed-citation><mixed-citation xml:lang="en">Rouce R. H., Shaim H., Sekine T., et al. The TGF-β/SMAD pathway is an important mechanism for NK cell immune evasion in childhood B-acute lymphoblastic leukemia. Leukemia. 2016; 30(4): 800-811. doi:10.1038/leu.2015.327</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">Nursal A. F., Pehlivan M., Sahin H. H., et al. The Associations of IL-6, IFN-γ, TNF-α, IL-10, and TGF-β1 Functional Variants with Acute Myeloid Leukemia in Turkish Patients. Genetic testing and molecular biomarkers. 2016; 20(9): 544-551. doi:10.1089/gtmb.2016.0036</mixed-citation><mixed-citation xml:lang="en">Nursal A. F., Pehlivan M., Sahin H. H., et al. The Associations of IL-6, IFN-γ, TNF-α, IL-10, and TGF-β1 Functional Variants with Acute Myeloid Leukemia in Turkish Patients. Genetic testing and molecular biomarkers. 2016; 20(9): 544-551. doi:10.1089/gtmb.2016.0036</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">Zhu B., Zhang J., Chen J., et al. Molecular biological characteristics of the recruitment of hematopoietic stem cells from bone marrow niche in chronic myeloid leukemia.Int J Clin Exp Pathol. 2015; 8:12595-607. PMID: 26722450; PMCID: PMC4680395.</mixed-citation><mixed-citation xml:lang="en">Zhu B., Zhang J., Chen J., et al. Molecular biological characteristics of the recruitment of hematopoietic stem cells from bone marrow niche in chronic myeloid leukemia.Int J Clin Exp Pathol. 2015; 8:12595-607. PMID: 26722450; PMCID: PMC4680395.</mixed-citation></citation-alternatives></ref><ref id="cit46"><label>46</label><citation-alternatives><mixed-citation xml:lang="ru">Yoshitake K., Hagiwara Y., Tanae K., et al. Marfan syndrome complicated with CD5+ CD10+ diffuse large B-cell lymphoma. Rinsho Ketsueki. 2010; 51:196-200. PMID: 20379114.</mixed-citation><mixed-citation xml:lang="en">Yoshitake K., Hagiwara Y., Tanae K., et al. Marfan syndrome complicated with CD5+ CD10+ diffuse large B-cell lymphoma. Rinsho Ketsueki. 2010; 51:196-200. PMID: 20379114.</mixed-citation></citation-alternatives></ref><ref id="cit47"><label>47</label><citation-alternatives><mixed-citation xml:lang="ru">Togashi Y., Sakoda H., Sugahara H., et al. Loeys-Dietz syndrome with acute myeloid leukemia. Rinsho Ketsueki. 2008; 49:664-7. PMID: 18800617.</mixed-citation><mixed-citation xml:lang="en">Togashi Y., Sakoda H., Sugahara H., et al. Loeys-Dietz syndrome with acute myeloid leukemia. Rinsho Ketsueki. 2008; 49:664-7. PMID: 18800617.</mixed-citation></citation-alternatives></ref><ref id="cit48"><label>48</label><citation-alternatives><mixed-citation xml:lang="ru">Papadopoulos A., Ntaios G., Kaiafa G., et al. Veno-occlusive disease of the liver during induction therapy for acute lymphoblastic leukemia.International journal of hematology. 2008; 88(4): 441-442. doi:10.1007/s12185-008-0172-6</mixed-citation><mixed-citation xml:lang="en">Papadopoulos A., Ntaios G., Kaiafa G., et al. Veno-occlusive disease of the liver during induction therapy for acute lymphoblastic leukemia.International journal of hematology. 2008; 88(4): 441-442. doi:10.1007/s12185-008-0172-6</mixed-citation></citation-alternatives></ref><ref id="cit49"><label>49</label><citation-alternatives><mixed-citation xml:lang="ru">Bell D., Marshman D. Diffuse large B cell lymphoma in a prosthetic aortic graft. Heart, Lung and Circulation. 2017; 26: e4-e6. doi:10.1016/j.hlc.2016.07.010</mixed-citation><mixed-citation xml:lang="en">Bell D., Marshman D. Diffuse large B cell lymphoma in a prosthetic aortic graft. Heart, Lung and Circulation. 2017; 26: e4-e6. doi:10.1016/j.hlc.2016.07.010</mixed-citation></citation-alternatives></ref><ref id="cit50"><label>50</label><citation-alternatives><mixed-citation xml:lang="ru">Ghosh S., Ghosh S., Kumar Ghosh S. Aortic aneurysm and non- Hodgkin’s lymphoma in Marfan syndrome. Turk J Haematol. 2009; 26:31-33. PMID: 27265107.</mixed-citation><mixed-citation xml:lang="en">Ghosh S., Ghosh S., Kumar Ghosh S. Aortic aneurysm and non- Hodgkin’s lymphoma in Marfan syndrome. Turk J Haematol. 2009; 26:31-33. PMID: 27265107.</mixed-citation></citation-alternatives></ref><ref id="cit51"><label>51</label><citation-alternatives><mixed-citation xml:lang="ru">Kerslake R., Hall M., Vagnarelli P., et al. A pancancer overview of FBN1, asprosin and its cognate receptor OR4M1 with detailed expression profiling in ovarian cancer. Oncol Lett. 2021;22(3):650. doi:10.3892/ol.2021.12911</mixed-citation><mixed-citation xml:lang="en">Kerslake R., Hall M., Vagnarelli P., et al. A pancancer overview of FBN1, asprosin and its cognate receptor OR4M1 with detailed expression profiling in ovarian cancer. Oncol Lett. 2021;22(3):650. doi:10.3892/ol.2021.12911</mixed-citation></citation-alternatives></ref><ref id="cit52"><label>52</label><citation-alternatives><mixed-citation xml:lang="ru">Davis M. R., Andersson R., Severin J. et al. Transcriptional profiling of the human fibrillin/LTBP gene family, key regulators of mesenchymal cell functions. Mol Genet Metab. 2014; 112:73-83. doi:10.1016/j.ymgme.2013.12.006</mixed-citation><mixed-citation xml:lang="en">Davis M. R., Andersson R., Severin J. et al. Transcriptional profiling of the human fibrillin/LTBP gene family, key regulators of mesenchymal cell functions. Mol Genet Metab. 2014; 112:73-83. doi:10.1016/j.ymgme.2013.12.006</mixed-citation></citation-alternatives></ref><ref id="cit53"><label>53</label><citation-alternatives><mixed-citation xml:lang="ru">Kudinova E. G. Carcinogenesis and violation of collagen formation. Medical Bulletin of the North Caucasus. 2016; 11(2): 330-334. (In Russ.) doi:10.14300/mnnc.2016.11069 @@Кудинова Е. Г. Канцерогенез и нарушение коллагенообразования. Медицинский вестник Северного Кавказа. 2016; 11(2): 330-334. doi:10.14300/mnnc.2016.11069</mixed-citation><mixed-citation xml:lang="en">Kudinova E. G. Carcinogenesis and violation of collagen formation. Medical Bulletin of the North Caucasus. 2016; 11(2): 330-334. (In Russ.) doi:10.14300/mnnc.2016.11069 @@Кудинова Е. Г. Канцерогенез и нарушение коллагенообразования. Медицинский вестник Северного Кавказа. 2016; 11(2): 330-334. doi:10.14300/mnnc.2016.11069</mixed-citation></citation-alternatives></ref><ref id="cit54"><label>54</label><citation-alternatives><mixed-citation xml:lang="ru">Kudinova E. G., Momot A. P. Hereditary connective tissue disorders and familial cancer: is there a relationship? Archive of Internal Medicine.2015; 4(24): 25-30. (In Russ.) @@Кудинова Е. Г., Момот А. П. Наследственный нарушения соединительной ткани и семейный рак: есть ли взаимосвязь? Архив внутренней медицины. 2015; 4(24): 25-30.</mixed-citation><mixed-citation xml:lang="en">Kudinova E. G., Momot A. P. Hereditary connective tissue disorders and familial cancer: is there a relationship? Archive of Internal Medicine.2015; 4(24): 25-30. (In Russ.) @@Кудинова Е. Г., Момот А. П. Наследственный нарушения соединительной ткани и семейный рак: есть ли взаимосвязь? Архив внутренней медицины. 2015; 4(24): 25-30.</mixed-citation></citation-alternatives></ref><ref id="cit55"><label>55</label><citation-alternatives><mixed-citation xml:lang="ru">Naumova L. A. General pathological aspects of atrophic lesions of the gastric mucosa: features of clinical and structural-functional manifestations of various morphogenetic variants of the atrophic process. - Moscow: Publishing House “Higher Education and Science”, 2013. 176 p. (In Russ.) @@Наумова JI.A. Общепатологические аспекты атрофического поражения слизистой оболочки желудка: особенности клинических и структурно-функциональных проявлений различных морфогенетических вариантов атрофического процесса. - М.: Издательский Дом «Высшее Образование и Наука», 2013. 176 с.</mixed-citation><mixed-citation xml:lang="en">Naumova L. A. General pathological aspects of atrophic lesions of the gastric mucosa: features of clinical and structural-functional manifestations of various morphogenetic variants of the atrophic process. - Moscow: Publishing House “Higher Education and Science”, 2013. 176 p. (In Russ.) @@Наумова JI.A. Общепатологические аспекты атрофического поражения слизистой оболочки желудка: особенности клинических и структурно-функциональных проявлений различных морфогенетических вариантов атрофического процесса. - М.: Издательский Дом «Высшее Образование и Наука», 2013. 176 с.</mixed-citation></citation-alternatives></ref><ref id="cit56"><label>56</label><citation-alternatives><mixed-citation xml:lang="ru">Naumova L. A., Osipova O. N., Shatalov V. G. Gastric cancer in patients with systemic undifferentiated connective tissue dysplasia: features of the clinic and morphology. Bulletin of SurGMU. The medicine. 2015; 3:26-31. (In Russ.) @@Наумова Л. А., Осипова О. Н., Шаталов В. Г. Рак желудка у пациентов с системной недифференцированной дисплазией соединительной ткани: особенности клиники и морфологии. Вестник СурГМУ. Медицина. 2015; 3:26-31.</mixed-citation><mixed-citation xml:lang="en">Naumova L. A., Osipova O. N., Shatalov V. G. Gastric cancer in patients with systemic undifferentiated connective tissue dysplasia: features of the clinic and morphology. Bulletin of SurGMU. The medicine. 2015; 3:26-31. (In Russ.) @@Наумова Л. А., Осипова О. Н., Шаталов В. Г. Рак желудка у пациентов с системной недифференцированной дисплазией соединительной ткани: особенности клиники и морфологии. Вестник СурГМУ. Медицина. 2015; 3:26-31.</mixed-citation></citation-alternatives></ref><ref id="cit57"><label>57</label><citation-alternatives><mixed-citation xml:lang="ru">Naumova L. A., Osipova O. N. The phenomenon of cyst formation as a possible marker of the violation of epithelial-stromal relations. Bulletin of SurGMU. The medicine. 2017; 3:62-67. (In Russ.) @@Наумова Л. А., Осипова О. Н. Феномен кистообразования как возможный маркер нарушения эпителио-стромальных отношений. Вестник СурГМУ. Медицина. 2017; 3:62-67.</mixed-citation><mixed-citation xml:lang="en">Naumova L. A., Osipova O. N. The phenomenon of cyst formation as a possible marker of the violation of epithelial-stromal relations. Bulletin of SurGMU. The medicine. 2017; 3:62-67. (In Russ.) @@Наумова Л. А., Осипова О. Н. Феномен кистообразования как возможный маркер нарушения эпителио-стромальных отношений. Вестник СурГМУ. Медицина. 2017; 3:62-67.</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>
