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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">82</article-id><article-id pub-id-type="doi">10.17650/2313-805X-2017-4-1-8-16</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">Actin isoforms and neoplastic transformation</article-title><trans-title-group xml:lang="ru"><trans-title>Изоформы актина и неопл астическая трансформация</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Dugina</surname><given-names>V. B.</given-names></name><name xml:lang="ru"><surname>Дугина</surname><given-names>В. Б.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>1, Build. 40 Leninskie Gory, Moscow 119992, Russia</p></bio><bio xml:lang="ru"><p>Россия, 119992 Москва, Ленинские горы, 1, стр. 40</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Shagieva</surname><given-names>G. S.</given-names></name><name xml:lang="ru"><surname>Шагиева</surname><given-names>Г. С.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>1, Build. 40 Leninskie Gory, Moscow 119992, Russia</p></bio><bio xml:lang="ru"><p>Россия, 119992 Москва, Ленинские горы, 1, стр. 40</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Khromova</surname><given-names>N. V.</given-names></name><name xml:lang="ru"><surname>Хромова</surname><given-names>Н. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>24 Kashirskoye Shosse, Moscow 115478, Russia</p></bio><bio xml:lang="ru"><p>Россия, 115478 Москва, Каширское шоссе, 24</p></bio><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Kopnin</surname><given-names>P. B.</given-names></name><name xml:lang="ru"><surname>Копнин</surname><given-names>П. Б.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>24 Kashirskoye Shosse, Moscow 115478, Russia</p></bio><bio xml:lang="ru"><p>Россия, 115478 Москва, Каширское шоссе, 24</p></bio><email>pbkopnin@mail.ru</email><xref ref-type="aff" rid="aff2"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">A.N. Belozerskiy Research Institute of Physico-Chemical Biology, M.V. Lomonosov Moscow State University</institution></aff><aff><institution xml:lang="ru">Научно-исследовательский институт физико-химической биологии им. А.Н. Белозерского ФГБОУ ВО «Московский государственный университет им. М.В. Ломоносова»</institution></aff></aff-alternatives><aff-alternatives id="aff2"><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">Научно-исследовательский институт канцерогенеза ФГБУ «Российский онкологический научный центр им. Н.Н. Блохина» Минздрава России</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2017-01-15" publication-format="electronic"><day>15</day><month>01</month><year>2017</year></pub-date><volume>4</volume><issue>1</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>8</fpage><lpage>16</lpage><history><date date-type="received" iso-8601-date="2017-04-18"><day>18</day><month>04</month><year>2017</year></date><date date-type="accepted" iso-8601-date="2017-04-18"><day>18</day><month>04</month><year>2017</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2017, Dugina V.B., Shagieva G.S., Khromova N.V., Kopnin P.B.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2017, Дугина В.Б., Шагиева Г.С., Хромова Н.В., Копнин П.Б.</copyright-statement><copyright-year>2017</copyright-year><copyright-holder xml:lang="en">Dugina V.B., Shagieva G.S., Khromova N.V., Kopnin P.B.</copyright-holder><copyright-holder xml:lang="ru">Дугина В.Б., Шагиева Г.С., Хромова Н.В., Копнин П.Б.</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/82">https://umo.abvpress.ru/jour/article/view/82</self-uri><abstract xml:lang="en"><p>The cytoplasmic actins (β and γ) play crucial roles during key cellular processes like adhesion, migration, polarization and cytokinesis. The understanding of their specific underlying mechanisms would be of major relevance not only for fundamental research but also for clinical applications, since modulations of actin isoforms are directly or indirectly correlated with severe pathologies. The major goal of the research was to elucidate the function of the actin isoforms during motile activities, adhesions and cell division and to investigate whether their expression and/or structural organization is related to pathological function. Selective depletion of β- and γ-cytoplasmic actins allowed attributing functional diversities of β- and γ-сytoplasmic actins. β-Сytoplasmic actin plays a preferential role in contractile activities, whereas γ-cytoplasmic actin mainly participates in the formation of a submembranous network necessary for cell shape flexibility and motile activity. The roles of isoforms in regulating the integrity of adherens and tight junctions respectively were demonstrated. Unique roles of β- and γ-cytoplasmic actins in normal cells were shown. Similar results were obtained in cancer cells compared with normal epithelial cells in culture and in human pathological tissue sections of mammary gland, colon, lung and cervix. Malignant cell transformation requires changes in the ability of cells to migrate. The disruption of actin cytoskeleton and intercellular adhesions is an important component of the acquisition of invasive properties in epithelial malignancies.</p></abstract><trans-abstract xml:lang="ru"><p/></trans-abstract><kwd-group xml:lang="en"><kwd>cytoplasmic actin isoform</kwd><kwd>β-actin</kwd><kwd>γ-actin</kwd><kwd>neoplastic transformation</kwd><kwd>tumor cell</kwd><kwd>cytoskeleton</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>цитоплазматическая изоформа актина</kwd><kwd>β-актин</kwd><kwd>γ-актин</kwd><kwd>неопластическая трансформация</kwd><kwd>опухолевая клетка</kwd><kwd>цитоскелет</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. Vandekerckhove J., Weber K. 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