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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">463</article-id><article-id pub-id-type="doi">10.17650/2313-805X-2022-9-3-15-23</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">Prospects for the use of statins in the treatment of neurofibromatosis type 1</article-title><trans-title-group xml:lang="ru"><trans-title>Перспективы применения статинов в лечении нейрофиброматоза 1-го типа</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-4091-382X</contrib-id><name-alternatives><name xml:lang="en"><surname>Mustafin</surname><given-names>R. N.</given-names></name><name xml:lang="ru"><surname>Мустафин</surname><given-names>Р. Н.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Rustam N. Mustafin.</p><p>3 Lenina St., Ufa 450008.</p></bio><bio xml:lang="ru"><p>Мустафин Рустам Наилевич.</p><p>450008 Уфа, ул. Ленина, 3.</p></bio><email>ruji79@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Bashkir State Medical University, Ministry of Health of Russia</institution></aff><aff><institution xml:lang="ru">ФГБОУ ВО «Башкирский государственный медицинский университет» Минздрава России</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2022-09-15" publication-format="electronic"><day>15</day><month>09</month><year>2022</year></pub-date><volume>9</volume><issue>3</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>15</fpage><lpage>23</lpage><history><date date-type="received" iso-8601-date="2022-10-07"><day>07</day><month>10</month><year>2022</year></date><date date-type="accepted" iso-8601-date="2022-10-07"><day>07</day><month>10</month><year>2022</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2022, Mustafin R.N.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2022, Мустафин Р.Н.</copyright-statement><copyright-year>2022</copyright-year><copyright-holder xml:lang="en">Mustafin R.N.</copyright-holder><copyright-holder xml:lang="ru">Мустафин Р.Н.</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/463">https://umo.abvpress.ru/jour/article/view/463</self-uri><abstract xml:lang="en"><p>Neurofibromatosis type 1 is caused by a germline mutation in the <italic>NF1</italic> gene encoding the tumor suppressor neurofibromin. Deficiency of this protein causes hyperactivation of Ras proto-oncogenes. This leads to the development of tumors. Ras proteins undergo prenylation, which is inhibited by inhibitors of 3-hydroxy-3-methylglutaryl-coenzyme-A reductase. Therefore, statins can be proposed as anticancer drugs in the complex treatment of neurofibromatosis type 1. Clinical studies have proven the effectiveness of statins in the treatment of sporadic malignant neoplasms, in the pathogenesis of which mutations in the <italic>NF1</italic> gene play an important role. Various pathways of the influence of these drugs on the development of tumors are described, including the activation of autophagy, ferroptosis, suppression of proliferation, stimulation of antitumor immunity, and effects on the microenvironment of neoplasms. Data on the effect of statins on the development and progression of neurofibromas in patients with neurofibromatosis type 1 are not presented in the scientific literature. However, it was found that statins enhance the effect of anticancer drugs, the use of which in monotherapy against malignant neoplasms associated with neurofibromatosis is ineffective. In this regard, despite the inefficiency of statins in cognitive disorders in patients with neurofibromatosis type 1, the introduction of these drugs into clinical practice in combination with other drugs could provide a pleiotropic effect, affect various links in the pathogenesis of the disease. </p></abstract><trans-abstract xml:lang="ru"><p>Нейрофиброматоз 1-го типа развивается вследствие герминальной мутации в гене <italic>NF1</italic>, кодирующем онкосупрессор нейрофибромин. дефицит данного белка вызывает гиперактивацию протоонкогенов Ras, что ведет к развитию опухолей. Белки Ras подвергаются пренилированию, которое подавляют ингибиторы 3-гидрокси-3-метилглутарил-коэнзим А редуктазы. поэтому они могут быть предложены как противоопухолевые препараты в комплексном лечении нейрофиброматоза 1-го типа. в клинических исследованиях была доказана эффективность статинов в терапии спорадических злокачественных новообразований, в патогенезе которых большую роль играют мутации в гене <italic>NF1</italic>. Описаны различные пути влияния этих препаратов на развитие опухолей, включая активацию аутофагии, ферроптоза, подавление пролиферации, стимуляцию противоопухолевого иммунитета и воздействие на микроокружение неоплазм. данных о воздействии статинов на развитие и прогрессирование нейрофибром у больных нейрофиброматозом 1-го типа в научной литературе не представлено. Однако выявлено, что они усиливают действие противоопухолевых препаратов, использование которых в монорежиме при ассоциированных с нейрофиброматозом злокачественных неоплазмах нерезультативно. в связи с этим, несмотря на неэффективность статинов при когнитивных расстройствах у пациентов с нейрофиброматозом 1-го типа, внедрение этих лекарственных средств в клиническую практику в комбинации с другими препаратами могло бы обеспечить плейотропный эффект, воздействовать на различные звенья патогенеза заболевания.</p></trans-abstract><kwd-group xml:lang="en"><kwd>malignant neoplasms</kwd><kwd>neurofibromatosis type 1</kwd><kwd>neurofibromin</kwd><kwd>oncosuppressor</kwd><kwd>tumors</kwd><kwd>proto-oncogenes</kwd><kwd>statins</kwd><kwd>cholesterol</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>злокачественные новообразования</kwd><kwd>нейрофиброматоз 1-го типа</kwd><kwd>нейрофибромин</kwd><kwd>онкосупрессор</kwd><kwd>опухоли</kwd><kwd>протоонкогены</kwd><kwd>статины</kwd><kwd>холестерин</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Baldo F., Grasso A.G., Wiel L.C. et al. 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