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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">Bone and soft tissue sarcomas, tumors of the skin</journal-id><journal-title-group><journal-title xml:lang="en">Bone and soft tissue sarcomas, tumors of the skin</journal-title><trans-title-group xml:lang="ru"><trans-title>Саркомы костей, мягких тканей и опухоли кожи</trans-title></trans-title-group></journal-title-group><issn publication-format="print">2219-4614</issn><issn publication-format="electronic">2782-3687</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">531</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>EXPERIMENTAL ONCOLOGY</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ЭКСПЕРИМЕНТАЛЬНАЯ ОНКОЛОГИЯ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">Molecular markers in diagnostics of bone tumors</article-title><trans-title-group xml:lang="ru"><trans-title>Молекулярные маркеры в диагностике опухолей костей</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Bulytcheva</surname><given-names>I. V.</given-names></name><name xml:lang="ru"><surname>Булычева</surname><given-names>Ирина Владиславовна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>irena@boulytcheva.com</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Soloviov</surname><given-names>Y. N.</given-names></name><name xml:lang="ru"><surname>Соловьев</surname><given-names>Ю. Н.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Kushlinskiy</surname><given-names>N. E.</given-names></name><name xml:lang="ru"><surname>Кушлинский</surname><given-names>Н. Е.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">FGBU N.N. Blokhin Russian Cancer Research Center</institution></aff><aff><institution xml:lang="ru">ФГБУ «Российский онкологический научный центр им. Н.Н. Блохина» РАМН</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2013-08-03" publication-format="electronic"><day>03</day><month>08</month><year>2013</year></pub-date><volume>5</volume><issue>3</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>73</fpage><lpage>78</lpage><history><date date-type="received" iso-8601-date="2022-02-03"><day>03</day><month>02</month><year>2022</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2013, Bulytcheva I.V., Soloviov Y.N., Kushlinskiy N.E.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2013, Булычева И.В., Соловьев Ю.Н., Кушлинский Н.Е.</copyright-statement><copyright-year>2013</copyright-year><copyright-holder xml:lang="en">Bulytcheva I.V., Soloviov Y.N., Kushlinskiy N.E.</copyright-holder><copyright-holder xml:lang="ru">Булычева И.В., Соловьев Ю.Н., Кушлинский Н.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://sarbon.abvpress.ru/jour/article/view/531">https://sarbon.abvpress.ru/jour/article/view/531</self-uri><abstract xml:lang="en"><p>There has been tremendous progress in the last decade in understanding of the behavior and molecular pathogenesis of sarcomas, which may ultimately lead to more effective therapy and prognostification for these rare malignancies. Bone and soft tissue sarcomas are uncommon group of tumors, they are histologically, behaviorally, and genetically diverse, and their pathogenesis is poorly understood. The increasing role of molecular diagnostics is up to date, this knowledge relates to the potential role of newer targeted therapies. The importance of multidisciplinary care, integration of histologic, molecular, radiographic and clinical data in the management of bone sarcomas is difficult to overestimate.</p></abstract><trans-abstract xml:lang="ru"><p>Генетический паспорт злокачественных опухолей в значительной мере предопределяет клиническое прогрессирование и прогноз онкологического заболевания. Современная морфологическая диагностика сарком костей невозможна без дополнительных методов исследования. Среди диагностических и прогностических критериев все большее значение приобретает иммунофенотипирование. новые молекулярные мишени (Bax, EGFR, Flt-1/ VEGFR1 Ab-1, Her-2/neu, Cox-2, p53,VEGF) находятся под пристальным вниманием исследователей для выявления агентов эффективной таргетной терапии.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>опухоли костей</kwd><kwd>молекулярные маркеры</kwd><kwd>патология</kwd><kwd>bone tumors</kwd><kwd>molecular markers</kwd><kwd>pathology</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Bovee J.V.M.G., Hogendoom P.C.W., Wunder J.S. et al. Cartilage tumors and bone development: molecular pathology and possible theraputic targets. Nat. Rev. Cancer. 2010, v. 10, p. 481-488.</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Cho H.Y., Lee M., Takei H. et al. Immunohistochemical comparison of chordoma with chondrosarcoma, myxopapillary ependymoma, chordoid meningioma. 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