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<article 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" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="other" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Advances in Molecular Oncology</journal-id><journal-title-group><journal-title xml:lang="en">Advances in Molecular Oncology</journal-title><trans-title-group xml:lang="ru"><trans-title>Успехи молекулярной онкологии</trans-title></trans-title-group></journal-title-group><issn publication-format="print">2313-805X</issn><issn publication-format="electronic">2413-3787</issn><publisher><publisher-name xml:lang="en">Publishing House ABV Press</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">379</article-id><article-id pub-id-type="doi">10.17650/2313-805X-2021-8-3-44-59</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>REVIEW ARTICLES</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ОБЗОРНЫЕ СТАТЬИ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">LYN kinase and estrogen receptor ERα: involvement in carcinogenesis and potential therapeutic target for tumors</article-title><trans-title-group xml:lang="ru"><trans-title>Рецептор эстрогенов ERα и киназа LYN: участие в механизмах канцерогенеза и использование в качестве мишеней в таргетной терапии при онкологических заболеваниях</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-8658-2819</contrib-id><name-alternatives><name xml:lang="en"><surname>Tikhonova</surname><given-names>V. V.</given-names></name><name xml:lang="ru"><surname>Тихонова</surname><given-names>В. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>24 Kashirskoe Shosse, Moscow 115478</p></bio><bio xml:lang="ru"><p>115478 Москва, Каширское шоссе, 24</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-6154-535X</contrib-id><name-alternatives><name xml:lang="en"><surname>Finashutina</surname><given-names>Y. P.</given-names></name><name xml:lang="ru"><surname>Финашутина</surname><given-names>Ю. П.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>24 Kashirskoe Shosse, Moscow 115478</p></bio><bio xml:lang="ru"><p>115478 Москва, Каширское шоссе, 24</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-8277-8649</contrib-id><name-alternatives><name xml:lang="en"><surname>Kesaeva</surname><given-names>L. A.</given-names></name><name xml:lang="ru"><surname>Кесаева</surname><given-names>Л. А.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>24 Kashirskoe Shosse, Moscow 115478</p></bio><bio xml:lang="ru"><p>115478 Москва, Каширское шоссе, 24</p></bio><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">N.N. Blokhin Russian Cancer Research Center, Ministry of Health of Russia</institution></aff><aff><institution xml:lang="ru">ФГБУ «Национальный медицинский исследовательский центр онкологии им. Н.Н. Блохина» Минздрава России</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2021-09-15" publication-format="electronic"><day>15</day><month>09</month><year>2021</year></pub-date><volume>8</volume><issue>3</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>44</fpage><lpage>59</lpage><history><date date-type="received" iso-8601-date="2021-11-05"><day>05</day><month>11</month><year>2021</year></date><date date-type="accepted" iso-8601-date="2021-11-05"><day>05</day><month>11</month><year>2021</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2021, Tikhonova V.V., Finashutina Y.P., Kesaeva L.A.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2021, Тихонова В.В., Финашутина Ю.П., Кесаева Л.А.</copyright-statement><copyright-year>2021</copyright-year><copyright-holder xml:lang="en">Tikhonova V.V., Finashutina Y.P., Kesaeva L.A.</copyright-holder><copyright-holder xml:lang="ru">Тихонова В.В., Финашутина Ю.П., Кесаева Л.А.</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://umo.abvpress.ru/jour/article/view/379">https://umo.abvpress.ru/jour/article/view/379</self-uri><abstract xml:lang="en"><p>Primary or secondary resistance is an important problem when treating any type of tumor. It is often associated with changes in target genes’ functioning. This raises the question of understanding functional intracellular interactions of genes and proteins in oncological processes and therapeutic resistance occurring. When searching target proteins of targeted therapy, it is necessary to identify biomolecules, participating in cell signaling life, which differ significantly in normal and oncological processes and interact with a large number of pathways. It is also important that these biomolecules are not an artifact of tumor therapy or cell line cultivation, and that it is possible to influence them directly, obtaining complex effect. In addition, it is important to study changes occurring during therapy with the biomolecules, which include proto-oncogene of SRC family kinase LYN and gene of the estrogen receptor α ESR1. All these factors may help to overcome the emerging resistance.Objective – to study the way genes of SRC kinase LYN and estrogen receptor α ESR1 influence oncological processes and occurrence of therapeutic resistance.</p></abstract><trans-abstract xml:lang="ru"><p>Важной проблемой при терапии любого типа опухоли является возникновение первичной или вторичной резистентности, которая зачастую связана с изменением функционирования целевых генов. В связи с этим встает вопрос о понимании функциональных внутриклеточных взаимодействий генов и белков в онкологических процессах и возникновении резистентности к лечению. Для поиска целевых белков таргетной терапии необходимо идентифицировать таких участников сигнальной жизни клетки, функциональное состояние которых различно в норме и при канцерогенезе. также важно, чтобы определение этих участников не было артефактом вследствие терапии опухолей или культивирования клеточных линий и существовала возможность оказывать на них прямое воздействие, дающее комплексный эффект. кроме того, необходимо изучить изменения, происходящие с этими участниками, к которым относятся киназы семейства SRC LYN и ген эстрогенового рецептора α, во время терапии в целях преодоления возникающей резистентности.</p><p>Цель обзора – изучение роли генов киназы семейства SRC LYN и эстрогенового рецептора α в онкологических процессах и возникновении резистентности к терапии.</p></trans-abstract><kwd-group xml:lang="en"><kwd>estrogen receptor α</kwd><kwd>SRC kinase</kwd><kwd>LYN</kwd><kwd>mutations</kwd><kwd>resistance</kwd><kwd>therapy prognosis</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>ген эстрогенового рецептора α</kwd><kwd>ген киназы семейства SRC LYN</kwd><kwd>мутации</kwd><kwd>резистентность</kwd><kwd>прогноз терапии</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Bilal E., Alexe G., Yao M. et al. 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