<?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">tiblj</journal-id><journal-title-group><journal-title xml:lang="ru">Туберкулез и болезни легких</journal-title><trans-title-group xml:lang="en"><trans-title>Tuberculosis and Lung Diseases</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2075-1230</issn><issn pub-type="epub">2542-1506</issn><publisher><publisher-name>Медицинские знания и технологии</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.21292/2075-1230-2021-99-12-38-43</article-id><article-id custom-type="elpub" pub-id-type="custom">tiblj-1597</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 ARTICLES</subject></subj-group></article-categories><title-group><article-title>Оценка роли полиморфизма rs2227983 гена EGFR в развитии аллергической бронхиальной астмы</article-title><trans-title-group xml:lang="en"><trans-title>Evaluation of the role of rs2227983 polymorphism of EGFR gene in the development of allergic asthma</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-9944-6568</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Аверьянов</surname><given-names>А. Б.</given-names></name><name name-style="western" xml:lang="en"><surname>Аveryanov</surname><given-names>A. B.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Аверьянов Анатолий Борисович, ассистент кафедры факультетской терапии с курсом ПО.</p><p>660022, г. Красноярск, ул. Партизана Железняка, д. 1.</p></bio><bio xml:lang="en"><p>Anatoliy B. Аveryanov, Assistant of Faculty Therapy Department with Professional Development Training.</p><p>1, Partizana Zheleznyaka St.,Krasnoyarsk, 660022.</p></bio><email xlink:type="simple">Averyanov_a007@mail.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/0000-0003-3825-3946</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Черкашина</surname><given-names>И. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Cherkashina</surname><given-names>I. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Черкашина Ирина Ивановна, доктор медицинских наук, профессор кафедры факультетской терапии с курсом ПО.</p><p>660022, г. Красноярск, ул. Партизана Железняка, д. 1.</p></bio><bio xml:lang="en"><p>Irina I. Cherkashina, Doctor of Medical Sciences, Professor of Faculty Therapy Department with Professional Development Training.</p><p>1, Partizana Zheleznyaka St.,Krasnoyarsk, 660022.</p></bio><email xlink:type="simple">cherkashina@list.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/0000-0002-6968-7627</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Никулина</surname><given-names>С. Ю.</given-names></name><name name-style="western" xml:lang="en"><surname>Nikulina</surname><given-names>S. Yu.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Никулина Светлана Юрьевна, доктор медицинских наук, профессор, заведующая кафедрой факультетской терапии с курсом ПО.</p><p>660022, г. Красноярск, ул. Партизана Железняка, д. 1.</p><p>Тел. 8 (391) 220-04-95.</p></bio><bio xml:lang="en"><p>Svetlana Yu. Nikulina, Doctor of Medical Sciences, Professor, Head of Faculty Therapy Department with Professional Development Training.</p><p>1, Partizana Zheleznyaka St.,Krasnoyarsk, 660022.</p><p>Phone: +7 (391) 220-04-95.</p></bio><email xlink:type="simple">nikulina@mail.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/0000-0002-8877-0805</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Кузнецова</surname><given-names>Е. Ю.</given-names></name><name name-style="western" xml:lang="en"><surname>Kuznetsova</surname><given-names>E. Yu.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Кузнецова Елена Юрьевна, кандидат медицинских наук, доцент кафедры факультетской терапии с курсом ПО.</p><p>660022, г. Красноярск, ул. Партизана Железняка, д. 1.</p></bio><bio xml:lang="en"><p>Elena Yu. Kuznetsova, Candidate of Medical Sciences, Associate Professor of Faculty Therapy Department with Professional Development Training.</p><p>1, Partizana Zheleznyaka St.,Krasnoyarsk, 660022.</p></bio><email xlink:type="simple">elenak002@mail.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>Максимов</surname><given-names>В. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Maksimov</surname><given-names>V. N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Максимов Владимир Николаевич, доктор медицинских наук, профессор, заведующий лабораторией молекулярно-генетических исследований терапевтических заболеваний.</p><p>630089, г. Новосибирск, ул. Бориса Богаткова, д. 175/1.</p><p>Тел.: 8 (383) 264-25-16.</p></bio><bio xml:lang="en"><p>Vladimir N. Maksimov, Doctor of Medical Sciences, Professor, Head of Laboratory for Molecular Genetic Research of Therapeutic Diseases.</p><p>175/1, Borisa Bogatkova St., Novosibirsk, 630089.</p><p>Phone: +7 (383) 264-25-16.</p></bio><email xlink:type="simple">medik11@mail.ru</email><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФГБОУ ВО «Красноярский государственный медицинский университет им. проф. В. Ф. Войно-Ясенецкого» МЗ РФ</institution><country>Россия</country></aff><aff xml:lang="en"><institution>V. F. Voyno-Yasenetsky Krasnoyarsk State Medical University</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>НИИ терапии и профилактической медицины ‒ филиал Института цитологии и генетики СО РАН</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Institute of Internal and Preventive Medicine, the Branch of Institute of Cytology and Genetics, the Siberian Branch of the Russian Academy of Sciences</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2021</year></pub-date><pub-date pub-type="epub"><day>12</day><month>01</month><year>2022</year></pub-date><volume>99</volume><issue>12</issue><fpage>38</fpage><lpage>43</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Аверьянов А.Б., Черкашина И.И., Никулина С.Ю., Кузнецова Е.Ю., Максимов В.Н., 2022</copyright-statement><copyright-year>2022</copyright-year><copyright-holder xml:lang="ru">Аверьянов А.Б., Черкашина И.И., Никулина С.Ю., Кузнецова Е.Ю., Максимов В.Н.</copyright-holder><copyright-holder xml:lang="en">Аveryanov A.B., Cherkashina I.I., Nikulina S.Y., Kuznetsova E.Y., Maksimov V.N.</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.tibl-journal.com/jour/article/view/1597">https://www.tibl-journal.com/jour/article/view/1597</self-uri><abstract><sec><title>Цель исследования</title><p>Цель исследования: изучение полиморфизма rs2227983 гена EGFR у больных аллергической бронхиальной астмой (БА) и у здоровых лиц.</p></sec><sec><title>Материалы и методы</title><p>Материалы и методы. В исследование включено 179 человек с аллергической БА. Диагноз, степень тяжести заболевания устанавливались в соответствии с рекомендациями GINA. Контрольная группа – практически здоровые индивиды (n = 217). Больным аллергической БА проводились стандартный набор лабораторных и инструментальных методов обследования и ДНК-типирование.</p></sec><sec><title>Результаты</title><p>Результаты. Установлено статистически значимое преобладание частоты встречаемости генотипа AG в группе больных с аллергической БА, в том числе среди женщин, по сравнению с группой здоровых лиц. Обнаружено, что генотип АG rs2227983 гена EGFR значимо чаще встречался у больных БА с легким и среднетяжелым течением, в том числе среди женщин, чем среди здоровых лиц, в том числе женщин.</p></sec><sec><title>Заключение</title><p>Заключение. Установлена ассоциация полиморфизма rs2227983 гена EGFR с аллергической БА. Гомозиготный генотип GG может играть протективную роль в отношении данного заболевания.</p></sec></abstract><trans-abstract xml:lang="en"><p>The objective of the study: to study rs2227983 polymorphism of EGFR gene in patients with allergic asthma and healthy individuals.</p><sec><title>Subjects and Methods</title><p>Subjects and Methods. 179 patients suffering from allergic asthma were included in the study. The diagnosis and degree of severity were established in accordance with the GINA recommendations. The Control Group included apparently healthy individuals (n = 217). Patients with allergic asthma underwent standard laboratory and instrumental examinations and DNA typing.</p></sec><sec><title>Results</title><p>Results. A statistically significant predominance of AG genotype frequency in the group of patients with allergic asthma, including women, versus the group of healthy individuals, was established. AG rs2227983 genotype of EGFR gene was found to be significantly more common in patients with mild and moderate allergic asthma including women, than in healthy individuals, including women.</p></sec><sec><title>Conclusion</title><p>Conclusion. The association of rs2227983 polymorphism of EGFR gene with allergic asthma has been established. A homozygous GG genotype may play a protective role against the disease.</p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>однонуклеотидный полиморфизм генов</kwd><kwd>бронхиальная астма</kwd><kwd>рецептор эпидермального фактора роста</kwd><kwd>rs2227983 гена EGFR</kwd></kwd-group><kwd-group xml:lang="en"><kwd>single-nucleotide gene polymorphism</kwd><kwd>bronchial asthma</kwd><kwd>epidermal growth factor receptor</kwd><kwd>rs2227983 EGFR gene</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">Генетика бронхолегочных заболеваний / под ред. В. П. Пузырева, Л. М. Огородовой. – М.: Атмосфера, 2010. – 160 с.</mixed-citation><mixed-citation xml:lang="en">Genetika bronkholegochnykh zabolevaniy. [Genetics of bronchopulmonary diseases]. V.P. Puzyrev, L.M. Ogorodova, eds., Moscow, Atmoshera Publ., 2010, 160 p.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Лебеденко А. А., Шкурат Т. П., Машкина Е. В., Семерник О. Е., Дрейзина Т. К. Анализ ассоциации полиморфных вариантов генов факторов роста с риском развития бронхиальной астмы у детей // Пульмонология. ‒ 2018. ‒ Т. 28, № 1. ‒ С. 7-12. DOI: org/10.18093/0869-0189-2018-28-1-7-12.</mixed-citation><mixed-citation xml:lang="en">Lebedenko А.А., Shkurat T.P., Mashkina E.V., Semernik O.E., Dreyzina T.K. An analysis of association between growth factor gene polymorphisms and the risk of bronchial asthma in children. Pulmonologiya, 2018, vol. 28, no. 1, pp. 7-12. (In Russ.) doi: org/10.18093/0869-0189-2018-28-1-7-12.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Миронова Ж. А., Трофимов В. И., Бабаджанова Г. Ю. Генетика бронхиальной астмы. Респираторная медицина. Руководство / под ред. акад. РАН А. Г. Чучалина, 2-е изд., перераб. и доп. Т. 1. ‒ С. 439-446.</mixed-citation><mixed-citation xml:lang="en">Mironova Zh.А., Trofimov V.I., Babadzhanova G.Yu. Genetika bronkhialnoy astmy. Respiratornaya meditisna. Rukovodstvo. [The genetics of bronchial asthma. Respiratory Medicine. Guidelines]. Chuchalin A.G., eds., 2nd ed., vol. 1, pp. 439-446.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Салтыкова И. В., Фрейдин М. Б., Брагина Е. Ю. и др. Ассоциация полиморфизма rs6737848 гена SOCS5 с бронхиальной астмой // Вестник Российской академии медицинских наук. ‒ 2013. ‒ № 7. ‒ С. 53-56.</mixed-citation><mixed-citation xml:lang="en">Saltykova I.V., Freydin M.B., Bragina E.Yu. et al. Association of rs6737848 polymorphism of the SOCS5 gene with bronchial asthma. Vestnik Rossiiskoy Akademii Meditsinskikh Nauk, 2013, no. 7, pp. 53-56. (In Russ.)</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Семерник О. Е., Лебеденко А. А., Шкурат Т. П., Машкина Е. В., Дрейзина Т. К. Роль мутаций генов металлопротеиназ и рецептора эпителиального фактора роста в патогенезе бронхиальной астмы у детей // Пульмонология. ‒ 2020. ‒ Т. 30, № 1. ‒ С. 17-22. DOI: org/10.18093/0869-0189-2020-30-1-17-22.</mixed-citation><mixed-citation xml:lang="en">Semernik O.E., Lebedenko А.А., Shkurat T.P., Mashkina E.V., Dreyzina T.K. The role of mutations in metalloproteinases and the epithelial growth factor receptor genes in the pathogenesis of children bronchial asthma. Pulmonologiya, 2020, vol. 30, no. 1, pp. 17-22. (In Russ.) doi: org/10.18093/0869-0189-2020-30-1-17-22.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Смит К., Калко С., Кантор Ч. Пульс-электрофорез и методы работы с большими молекулами ДНК. Анализ генома / под ред. К. Дейвиса. ‒ М: Мир, 1990. ‒ С. 58-94.</mixed-citation><mixed-citation xml:lang="en">Smith K., Calko S., Cantor Ch. Puls-elektroforez i metody raboty s bolshimi molekulami DNK. Analiz genoma. (Russ. Ed.: Smith K., Calko S., Cantor Ch. Pulse electrophoresis and methods for working with large DNA molecules. In: Genome analysis. A practical approach by K.E. Davies). Moscow, Mir Publ., 1990. pp. 58-94.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Albitar L., Pickett G., Morgan M. et al. EGFR isoforms and gene regulation in human endometrial cancer cells // Molecular Cancer. ‒ 2010. ‒ № 9. ‒ С. 166. DOI: 10.1186/1476-4598-9-166.</mixed-citation><mixed-citation xml:lang="en">Albitar L., Pickett G., Morgan M. et al. EGFR isoforms and gene regulation in human endometrial cancer cells. Molecular Cancer, 2010, no. 9, pp. 166. doi: 10.1186/1476-4598-9-166.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Bai J., Guo X. G., Bai X. P. Epidermal growth factor receptor-related DNA repair and radiationresistance regulatory mechanisms: a mini-review // Asia Pac. J. Cancer Prevent. ‒ 2012. ‒ № 13. ‒ Р. 4879-4881. DOI: 10.7314/apjcp.2012.13.10.4879.</mixed-citation><mixed-citation xml:lang="en">Bai J., Guo X. G., Bai X.P. Epidermal growth factor receptor-related DNA repair and radiationresistance regulatory mechanisms: a mini-review. Asia Pac. J. Cancer Prevent., 2012, no. 13, pp. 4879-4881. doi: 10.7314/apjcp.2012.13.10.4879.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Barnes P. J. Immunology of asthma and chronic obstructive pulmonary disease // Nat. Rev. Immunol. – 2008. – Vol. 8, № 3. – P. 183-192.</mixed-citation><mixed-citation xml:lang="en">Barnes P.J. Immunology of asthma and chronic obstructive pulmonary disease. Nat. Rev. Immunol., 2008, vol. 8, no. 3, pp. 183-192.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Bouzigon E., Nadif R., Moual N. Le et al. Genetic and environmental factors of asthma and allergy: Results of the EGEA study // Rev. Mal. Respir. – 2015. – Mar. 17.</mixed-citation><mixed-citation xml:lang="en">Bouzigon E., Nadif R., Moual N.Le et al. Genetic and environmental factors of asthma and allergy: Results of the EGEA study. Rev. Mal. Respir., 2015, Mar. 17.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Gerger A., El-Khoueiry A., Zhang W. et al. Pharmacogenetic angiogenesis profiling for firstlineBevacizumab plus oxaliplatin-based chemotherapy in patients with metastatic colorectalcancer // Clin. Cancer Res. ‒ 2011. ‒ № 17. ‒ Р. 5783-5792. DOI: 10.1158/1078-0432.CCR-11-1115.</mixed-citation><mixed-citation xml:lang="en">Gerger A., El-Khoueiry A., Zhang W. et al. Pharmacogenetic angiogenesis profiling for firstlineBevacizumab plus oxaliplatin-based chemotherapy in patients with metastatic colorectalcancer. Clin. Cancer Res., 2011, no. 17, pp. 5783-5792. doi: 10.1158/1078-0432.CCR-11-1115.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Hsu S. C., Miller S. A., Wang Y., Hung M. C. Nuclear EGFR is required for cisplatin resistance and DNA repair // Am. J. Transl. Res. ‒ 2009. № 1. ‒ Р. 249-258. DOI: 10.1158/0008-5472.can-10-2384.</mixed-citation><mixed-citation xml:lang="en">Hsu S.C., Miller S.A., Wang Y., Hung M.C. Nuclear EGFR is required for cisplatin resistance and DNA repair. Am. J. Transl. Res., 2009, no. 1, pp. 249-258. doi: 10.1158/0008-5472.can-10-2384.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Huang C. M., Chen H. H., Chen D. C. et al. Rheumatoid arthritis is associated with rs17337023 polymorphism and increased serum level of the EGFR protein // PLoS One. – 2017. – Vol. 12, № 7. – P. 180604.</mixed-citation><mixed-citation xml:lang="en">Huang C.M., Chen H.H., Chen D.C. et al. Rheumatoid arthritis is associated with rs17337023 polymorphism and increased serum level of the EGFR protein. PLoS One, 2017, vol. 12, no. 7, pp. 180604.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Karmaus W., Ziyab A.H., Everson T. et al. Epigenetic mechanisms and models in the origins of asthma // Curr. Opin. Allergy Clin. Immunol. – 2013. – Vol. 13, № 1. – P. 63-69.</mixed-citation><mixed-citation xml:lang="en">Karmaus W., Ziyab A.H., Everson T. et al. Epigenetic mechanisms and models in the origins of asthma. Curr. Opin. Allergy Clin. Immunol., 2013, vol. 13, no. 1, pp. 63-69.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Le Cras T. D., Acciani T. H., Mushaben E. M. et al. Epithelial EGF receptor signaling mediates airway hyperreactivity and remodeling in a mouse model of chronic asthma // Am. J. Physiol. Lung Cell Mol. Physiolog. ‒ 2011. ‒ Vol. 300, № 3. ‒ Р. 414-421. DOI: 10.1152/ajplung.00346.2010.</mixed-citation><mixed-citation xml:lang="en">Le Cras T.D., Acciani T.H., Mushaben E.M. et al. Epithelial EGF receptor signaling mediates airway hyperreactivity and remodeling in a mouse model of chronic asthma. Am. J. Physiol. Lung Cell Mol. Physiolog., 2011, vol. 300, no. 3, pp. 414-421. doi: 10.1152/ajplung.00346.2010.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Li C., Wei R., Jones-Hall Y. L. et al. Epidermal growth factor receptor (EGFR) pathway genesand interstitial lung disease: an association study // Sci. Reports. ‒ 2014. ‒ № 4. ‒ Р. 4893.DOI: 10.1038/srep04893.</mixed-citation><mixed-citation xml:lang="en">Li C., Wei R., Jones-Hall Y.L. et al. Epidermal growth factor receptor (EGFR) pathway genes and interstitial lung disease: an association study. Sci. Reports, 2014, no. 4, pp. 4893. doi: 10.1038/srep04893.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Rodemann H. P., Dittmann K., Toulany M. Radiation-induced EGFR-signaling and control of DNA-damage repair // Int. J. Radiat. Biol. ‒ 2007. ‒ № 83. ‒ Р. 781-791. DOI: 10.1080/09553000701769970.</mixed-citation><mixed-citation xml:lang="en">Rodemann H.P., Dittmann K., Toulany M. Radiation-induced EGFR-signaling and control of DNA-damage repair. Int. J. Radiat. Biol., 2007, no. 83, pp. 781-791. doi: 10.1080/09553000701769970.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Sharma S. V., Bell D. W., Settleman J., Haber D. A. Epidermal growth factor receptor mutations in lung cancer // Nat. Rev. Cancer. ‒ 2007. ‒ № 7. ‒ Р. 169-181. DOI: 10.1038/nrc2088.</mixed-citation><mixed-citation xml:lang="en">Sharma S.V., Bell D.W., Settleman J., Haber D.A. Epidermal growth factor receptor mutations in lung cancer. Nat. Rev. Cancer, 2007, no. 7, pp. 169-181. doi: 10.1038/nrc2088.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Wiley H. S. Trafficking of the ErbB receptors and its influence on signaling // The EGF Receptor Family. – 2003. – Р. 8-91.</mixed-citation><mixed-citation xml:lang="en">Wiley H.S. Trafficking of the ErbB receptors and its influence on signaling. The EGF Receptor Family. 2003, pp. 8-91.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Yoshikawa T., Kanazawa H. Integrated effect of EGFR and PAR-1 signaling crosstalk on air way hyperrespon siveness // Int. J. Mol. Med. ‒ 2012. ‒ Vol. 30, № 1. ‒ Р. 41-48. DOI: 10.3892/ijmm.2012.981.</mixed-citation><mixed-citation xml:lang="en">Yoshikawa T., Kanazawa H. Integrated effect of EGFR and PAR-1 signaling crosstalk on air way hyperrespon siveness. Int. J. Mol. Med., 2012, vol. 30, no. 1, pp. 41-48. doi: 10.3892/ijmm.2012.981.</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>
