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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">216</article-id><article-id pub-id-type="doi">10.17650/2313-805X-2019-6-2-28-41</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">Promises of targeted therapy for low grade gliomas in children</article-title><trans-title-group xml:lang="ru"><trans-title>Перспективы таргетной терапии глиом низкой степени злокачественности у детей</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-2977-665X</contrib-id><name-alternatives><name xml:lang="en"><surname>Valiakhmetova</surname><given-names>E. F.</given-names></name><name xml:lang="ru"><surname>Валиахметова</surname><given-names>Э. Ф.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>16, 4th Tverskaya-Yamskaya St., Moscow 125047</p></bio><bio xml:lang="ru"><p>125047 Москва, ул. 4-я Тверская-Ямская, 16</p></bio><email>andgeval@gmail.com</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-3007-3772</contrib-id><name-alternatives><name xml:lang="en"><surname>Yasko</surname><given-names>L. A.</given-names></name><name xml:lang="ru"><surname>Ясько</surname><given-names>Л. А.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>1 Samory Mashela St., Moscow 117997</p></bio><bio xml:lang="ru"><p>117997 Москва, ГСП-7, ул. Саморы Машела, 1</p></bio><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-7750-5216</contrib-id><name-alternatives><name xml:lang="en"><surname>Papusha</surname><given-names>L. I.</given-names></name><name xml:lang="ru"><surname>Папуша</surname><given-names>Л. И.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>1 Samory Mashela St., Moscow 117997</p></bio><bio xml:lang="ru"><p>117997 Москва, ГСП-7, ул. Саморы Машела, 1</p></bio><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-1308-8622</contrib-id><name-alternatives><name xml:lang="en"><surname>Druy</surname><given-names>A. E.</given-names></name><name xml:lang="ru"><surname>Друй</surname><given-names>А. Е.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>1 Samory Mashela St., Moscow 117997</p></bio><bio xml:lang="ru"><p>117997 Москва, ГСП-7, ул. Саморы Машела, 1</p></bio><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Karachunsky</surname><given-names>A. I.</given-names></name><name xml:lang="ru"><surname>Карачунский</surname><given-names>А. И.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>1 Samory Mashela St., Moscow 117997;  1 Ostrovitianova St., Moscow 117997</p></bio><bio xml:lang="ru"><p>117997 Москва, ГСП-7, ул. Саморы Машела, 1; 117997 Москва, ул. Островитянова, 1</p></bio><xref ref-type="aff" rid="aff2"/><xref ref-type="aff" rid="aff3"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">N.N. Burdenko National Scientific and Practical Center for Neurosurgery , Ministry of Health of Russia</institution></aff><aff><institution xml:lang="ru">ФГАУ «Национальный медицинский исследовательский центр нейрохирургии им. акад. Н. Н. Бурденко» Минздрава России</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology</institution></aff><aff><institution xml:lang="ru">ФГБУ «Национальный медицинский исследовательский центр детской гематологии, онкологии и иммунологии им. Дмитрия Рогачева» Минздрава России</institution></aff></aff-alternatives><aff-alternatives id="aff3"><aff><institution xml:lang="en">N.I. Pirogov Russian National Research Medical University</institution></aff><aff><institution xml:lang="ru">ФГБОУ ВО «Российский национальный исследовательский медицинский университет им. Н. И. Пирогова» Минздрава России</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2019-05-15" publication-format="electronic"><day>15</day><month>05</month><year>2019</year></pub-date><volume>6</volume><issue>2</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>28</fpage><lpage>41</lpage><history><date date-type="received" iso-8601-date="2019-07-27"><day>27</day><month>07</month><year>2019</year></date><date date-type="accepted" iso-8601-date="2019-07-27"><day>27</day><month>07</month><year>2019</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2019, Valiakhmetova E.F., Yasko L.A., Papusha L.I., Druy A.E., Karachunsky A.I.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2019, Валиахметова Э.Ф., Ясько Л.А., Папуша Л.И., Друй А.Е., Карачунский А.И.</copyright-statement><copyright-year>2019</copyright-year><copyright-holder xml:lang="en">Valiakhmetova E.F., Yasko L.A., Papusha L.I., Druy A.E., Karachunsky A.I.</copyright-holder><copyright-holder xml:lang="ru">Валиахметова Э.Ф., Ясько Л.А., Папуша Л.И., Друй А.Е., Карачунский А.И.</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/216">https://umo.abvpress.ru/jour/article/view/216</self-uri><abstract xml:lang="en"><p>Low grade gliomas are the most common brain tumors in children. Total resection for operable lesion helps to achieve local and system control. Nevertheless, for inaccessible tumors are required more effective treatment both to overcome the refractory course of the disease, and to mi nimize toxicity with conventional adjuvant chemotherapy and various types of radiation therapy. In recent years, there has been an accelerated understanding of the molecular pathogenesis of some tumors in children, including low grade gliomas. Given the fact that the basis of the molecular pathogenesis of the low grade gliomas is the activation of signaling pathways MARK (mitogen activated protein kinase) and mTOR (mammalian target of rapamycin), the most promising targeted agents are BRAF, MEK and mTOR inhibitors. Nevertheless, a number of other agents have been studied to find promising targeted therapy for this tumors type. This article summarizes the latest literature evaluating new drugs in low grade glioma.</p></abstract><trans-abstract xml:lang="ru"><p>Глиомы низкой степени злокачественности являются преобладающим большинством в структуре опухолей головного мозга у детей. Достичь локального и системного контроля над опухолью возможно при полном удалении образования. Сложная локализация глубоко расположенных и диффузно растущих опухолей ограничивает объем оперативного вмешательства и требует поиска, а также совершенствования методов консервативного лечения данной нозологической группы. Необходимы более эффективные виды лечения как для преодоления рефрактерного течения заболевания, так и для минимизации токсичности, связанной с обычной адъювантной химиотерапией и различными видами лучевой терапии. С учетом того, что в основе молекулярного патогенеза большинства глиом низкой степени злокачественности лежит активация сигнальных путей МАРК (mitogen activated protein kinase) и mTOR (мишени рапамицина млекопитающих), наиболее перспективными агентами – таргетными препаратами являются BRAF, MEK и mTOR-ингибиторы. Тем не менее целый ряд других соединений был исследован в целях поиска перспективных агентов для таргетной терапии при опухолях указанного типа. Обзор суммирует новейшие данные литературы, посвященной новым препаратам при глиоме низкой степени злокачественности.</p></trans-abstract><kwd-group xml:lang="en"><kwd>low grade gliomas</kwd><kwd>targeted therapy</kwd><kwd>BRAF:KIAA1549 fusion</kwd><kwd>BRAFV600 mutation</kwd><kwd>subependymal giant cell astrocytoma</kwd><kwd>mTOR</kwd><kwd>tyrosine kinase inhibitor</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>глиома низкой степени злокачественности</kwd><kwd>таргетная терапия</kwd><kwd>слияние BRAF:KIAA1549</kwd><kwd>мутация BRAFV600</kwd><kwd>субэпендимальная гигантоклеточная астроцитома</kwd><kwd>mTOR</kwd><kwd>ингибитор тирозинкиназы</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Ostrom Q.T., Gittleman H., Liao P. et al. CBTRUS statistical report: primary brain and central nervous system tumors diagnosed in the United States in 2007–2011. Neuro Oncol 2014;16(Suppl 4):iv1–63. 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