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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">59</article-id><article-id pub-id-type="doi">10.17650/2313-805X.2016.3.2.26-33</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">Tumor stem cells from glioblastoma multiforme</article-title><trans-title-group xml:lang="ru"><trans-title>Опухолевые стволовые клетки мультиформной глиобластомы</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Nikiforova</surname><given-names>Z. N.</given-names></name><name xml:lang="ru"><surname>Никифорова</surname><given-names>З. Н.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>zojanik@rambler.ru</email><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Kudryavtsev</surname><given-names>I. A.</given-names></name><name xml:lang="ru"><surname>Кудрявцев</surname><given-names>И. А.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Arnotskaya</surname><given-names>N. E.</given-names></name><name xml:lang="ru"><surname>Арноцкая</surname><given-names>Н. Е.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Bryukhovetskiy</surname><given-names>I. S.</given-names></name><name xml:lang="ru"><surname>Брюховецкий</surname><given-names>И. С.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff3"/><xref ref-type="aff" rid="aff4"/><xref ref-type="aff" rid="aff5"/><xref ref-type="aff" rid="aff6"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Shevchenko</surname><given-names>V. E.</given-names></name><name xml:lang="ru"><surname>Шевченко</surname><given-names>В. Е.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Research Institute of Carcinogenesis, N.N. Blokhin Russian Cancer Research Center, Ministry of Health of Russia</institution></aff><aff><institution xml:lang="ru">НИИ канцерогенеза ФГБУ «РОНЦ им. Н. Н. Блохина» Минздрава России</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">24 Kashirskoe Shosse, Moscow, 115478, Russia</institution></aff><aff><institution xml:lang="ru">Россия, 115478, Москва, Каширское шоссе, 24</institution></aff></aff-alternatives><aff-alternatives id="aff3"><aff><institution xml:lang="en">Biomedicine School, Far Eastern Federal University</institution></aff><aff><institution xml:lang="ru">Школа биомедицины ФГАОУ ВПО «Дальневосточный федеральный университет»</institution></aff></aff-alternatives><aff-alternatives id="aff4"><aff><institution xml:lang="en">8 Sukhanova St., Vladivostok, 690091, Russia</institution></aff><aff><institution xml:lang="ru">Россия, 690091, Владивосток, ул. Суханова, 8</institution></aff></aff-alternatives><aff-alternatives id="aff5"><aff><institution xml:lang="en">A.V. Zhirmunskiy Institute of Sea Biology, Far Eastern Brach, Russian Academy of Sciences</institution></aff><aff><institution xml:lang="ru">ФГБУН «Институт биологии моря им. А. В. Жирмунского» Дальневосточного отделения Российской академии наук</institution></aff></aff-alternatives><aff-alternatives id="aff6"><aff><institution xml:lang="en">17 Pal’chevskogo St., Vladivostok, 690059, Russia</institution></aff><aff><institution xml:lang="ru">Россия, 690059, Владивосток, ул. Пальчевского, 17</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2016-05-15" publication-format="electronic"><day>15</day><month>05</month><year>2016</year></pub-date><volume>3</volume><issue>2</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>26</fpage><lpage>33</lpage><history><date date-type="received" iso-8601-date="2016-06-07"><day>07</day><month>06</month><year>2016</year></date><date date-type="accepted" iso-8601-date="2016-06-07"><day>07</day><month>06</month><year>2016</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2016, Nikiforova Z.N., Kudryavtsev I.A., Arnotskaya N.E., Bryukhovetskiy I.S., Shevchenko V.E.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2016, Никифорова З.Н., Кудрявцев И.А., Арноцкая Н.Е., Брюховецкий И.С., Шевченко В.Е.</copyright-statement><copyright-year>2016</copyright-year><copyright-holder xml:lang="en">Nikiforova Z.N., Kudryavtsev I.A., Arnotskaya N.E., Bryukhovetskiy I.S., Shevchenko V.E.</copyright-holder><copyright-holder xml:lang="ru">Никифорова З.Н., Кудрявцев И.А., Арноцкая Н.Е., Брюховецкий И.С., Шевченко В.Е.</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/59">https://umo.abvpress.ru/jour/article/view/59</self-uri><abstract xml:lang="en"><p>Glioblastoma multiforme, a World Health Organization grade IV malignant glioma, is the most common and lethal primary brain tumor with the median survival of approximately 15–25 months after treatment. Glioblastoma multiforme has been shown to be resistant to radiotherapy and chemotherapy and invariably recurs following surgical resection and chemoradiation. The characteristics of this tumor are exemplified by heterogeneous cell population with diverse biologic properties and genetic changes, the ability to form cancer stem cells (CSC) and divided into four molecular subtypes – proneural, neural, classical and mesenchymal. Despite some success, the mechanisms leading to the formation of the most malignant tumor subtype are unclear. The aim of this review was a synthesis of modern information about the role and biological characteristics of tumor stem cells in tumor progression and the pathogenesis of glioblastoma multiforme. CSCs reside in niches, which are anatomically distinct regions within the tumor microenvironment. These niches maintain the principle properties of CSCs, preserve their phenotypic plasticity, adhesion, survival, resistance to standard cancer treatment and metastatic potential. The presence of aberrant signaling pathways (Notch, Hedgehog-Gli, Wnt/β-catenin, TGF-β/SMAD, PI3K/Akt/mTOR), both in the tumor and in the population of CSC, the dysregulation of microRNAs (miR-21, miR-128, miR-326, miR-34a), influence of epithelial-to-mesenchymal transition explains the availability of typical biological characteristics of the CSC. One needs to consider the influence of the therapy on normal stem cells in the development of drugs directed against the CSC. Regulatory mechanisms and markers found over the last decade can be used as the basis for creation of the new drugs with targeted action in the treatment of glioblastoma multiforme.</p></abstract><trans-abstract xml:lang="ru"><p/></trans-abstract><kwd-group xml:lang="en"><kwd>glioblastoma multiforme</kwd><kwd>cancer stem cell</kwd><kwd>CD 133+ marker</kwd><kwd>Notch-signaling pathway</kwd><kwd>Hedgehog-Gli-signaling pathway</kwd><kwd>Wnt/ β-catenin-signaling pathway</kwd><kwd>TGF-β/SMAD-signaling pathway</kwd><kwd>epithelial – mesenchymal transition</kwd><kwd>microRNA</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>мультиформная глиобластома</kwd><kwd>опухолевая стволовая клетка</kwd><kwd>маркер CD133+</kwd><kwd>Notch-сигнальный путь</kwd><kwd>Hedgehog-Gli- сигнальный путь</kwd><kwd>Wnt/β-катенин-сигнальный путь</kwd><kwd>TGF-β/SMAD-сигнальный путь</kwd><kwd>эпителиально-мезенхимальный переход</kwd><kwd>микроРНК</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><citation-alternatives><mixed-citation xml:lang="en">1. 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