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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">Cancer Urology</journal-id><journal-title-group><journal-title xml:lang="en">Cancer Urology</journal-title><trans-title-group xml:lang="ru"><trans-title>Онкоурология</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1726-9776</issn><issn publication-format="electronic">1996-1812</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">626</article-id><article-id pub-id-type="doi">10.17650/1726-9776-2017-13-1-20-26</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>DIAGNOSIS AND TREATMENT OF URINARY SYSTEM TUMORS. RENAL CANCER</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ДИАГНОСТИКА И ЛЕЧЕНИЕ ОПУХОЛЕЙ МОЧЕПОЛОВОЙ СИСТЕМЫ. Рак почки</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">Role of tumor-associated macrophages in renal cell carcinoma pathogenesis</article-title><trans-title-group xml:lang="ru"><trans-title>Роль макрофагов, ассоциированных с опухолью в патогенезе почечно-клеточного рака</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Kovaleva</surname><given-names>O. V.</given-names></name><name xml:lang="ru"><surname>Ковалева</surname><given-names>О. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>24 Kashirskoe Shosse, Moscow 115478</p></bio><bio xml:lang="ru"><p>115478 Москва, Каширское шоссе, 24</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Efremov</surname><given-names>G. D.</given-names></name><name xml:lang="ru"><surname>Ефремов</surname><given-names>Г. Д.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>3 2nd Botkinskiy Proezd, Moscow 125284</p></bio><bio xml:lang="ru"><p>125284 Москва, 2-й Боткинский проезд, 3</p></bio><email>efremov.gen@yandex.ru</email><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Mikhaylenko</surname><given-names>D. S.</given-names></name><name xml:lang="ru"><surname>Михайленко</surname><given-names>Д. С.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>3 2nd Botkinskiy Proezd, Moscow 125284</p></bio><bio xml:lang="ru"><p>125284 Москва, 2-й Боткинский проезд, 3</p></bio><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Alekseev</surname><given-names>B. Ya.</given-names></name><name xml:lang="ru"><surname>Алексеев</surname><given-names>Б. Я.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>3 2nd Botkinskiy Proezd, Moscow 125284</p></bio><bio xml:lang="ru"><p>125284 Москва, 2-й Боткинский проезд, 3</p></bio><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Grachev</surname><given-names>A. N.</given-names></name><name xml:lang="ru"><surname>Грачев</surname><given-names>А. Н.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>24 Kashirskoe Shosse, Moscow 115478</p></bio><bio xml:lang="ru"><p>Алексей Николаевич Грачев</p><p>115478 Москва, Каширское шоссе, 24</p></bio><email>alexei.gratchev@gmail.com</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Blokhin Russian Cancer Research Center</institution></aff><aff><institution xml:lang="ru">Российский онкологический научный центр им. Н.Н. Блохина</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">National Medical Research Radiological Center</institution></aff><aff><institution xml:lang="ru">Национальный медицинский исследовательский радиологический центр</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2017-03-30" publication-format="electronic"><day>30</day><month>03</month><year>2017</year></pub-date><volume>13</volume><issue>1</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>20</fpage><lpage>26</lpage><history><date date-type="received" iso-8601-date="2016-10-31"><day>31</day><month>10</month><year>2016</year></date><date date-type="accepted" iso-8601-date="2016-12-22"><day>22</day><month>12</month><year>2016</year></date></history><permissions><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/></permissions><self-uri xlink:href="https://oncourology.abvpress.ru/oncur/article/view/626">https://oncourology.abvpress.ru/oncur/article/view/626</self-uri><abstract xml:lang="en"><p>The role of tumor stroma in malignant tumor pathogenesis cannot be disputed. Macrophages are one of the crucial elements of tumor stroma. Tumor-associated macrophages (TAMs) are type 2-activated macrophages (M2). They were first described in 1992. They carry CD206, CD163, FXIIIa, βIG-H3, stabilin 1, YKL-39, SI-CLP, tenascin С, LOX-1, fibronectin, MARCO, interleukin 1 receptor antagonist (IL-1RA) and other markers. Unlike proinflammatory macrophages (M1), М2 display high anti-inflammatory activity and are responsible for inflammation reaction suppression and tissue recovery in inflamed area. TAMs significantly contribute to tumor progression by stimulating cell proliferation, angiogenesis, and suppression of antitumor immune response. Identification of macrophages in renal tumors involves a limited number of markers, which doesn’t allow making a conclusive answer about their function. However, a correlation between TAMs content and a negative disease prognosis can be considered proven. Studies of M1 and M2 using different markers have shown that renal tumors contain high levels of TAMs with mixed M1/M2 phenotype. TAMs in renal tumors are highly proangiogenic and immunosuppressive. TAMs density can be used as a prognostic marker, but development of an effective treatment strategy aimed at inhibition of TAMs antitumor activity requires systemic research involving a wide panel of M1 and M2 macrophage markers. </p></abstract><trans-abstract xml:lang="ru"><p>Роль опухолевой стромы в патогенезе злокачественных опухолей не подвергается сомнению. Макрофаги – одни из ключевых элементов опухолевой стромы. Макрофаги, ассоциированные с опухолью (МАО), являются макрофагами 2-го типа активации (М2), которые впервые были описаны в1992 г. К их маркерам относятся CD206, CD163, FXIIIa, βIG-H3, стабилин 1, YKL-39, SI–CLP, тенасцин С, LOX-1, MARCO, фибронектин, антагонист рецептора интерлейкина 1 (ИЛ-1RA) и др. В отличие от провоспалительных макрофагов (М1) М2 обладают выраженной противовоспалительной активностью и отвечают за подавление воспалительной реакции и восстановление ткани в очаге воспаления. МАО вносят значительный вклад в прогрессию опухолей за счет стимуляции пролиферации клеток, ангиогенеза и подавления противоопухолевого иммунного ответа. Для выявления макрофагов в опухолях почки используют ограниченное количество маркеров, не позволяющих сделать однозначного вывода относительно их функции. Однако несмотря на это, ассоциацию количества МАО с плохим прогнозом заболевания можно считать доказанной. Исследования фенотипа М1 и М2 с использованием их различных маркеров показали, что в опухолях почки присутствует большое количество МАО, имеющих смешанный М1/М2-фенотип. МАО в опухолях почки обладают выраженными проангиогенными и иммуносупрессорными свойствами. Хотя плотность МАО может быть использована в качестве прогностического маркера, необходимы систематические исследования с применением широкой панели маркеров М1 и М2 для разработки эффективной стратегии лечения, направленной на нейтрализацию проопухолевой активности МАО.</p></trans-abstract><kwd-group xml:lang="en"><kwd>macrophage</kwd><kwd>cytokine</kwd><kwd>renal cell carcinoma</kwd><kwd>tumor-associated macrophages</kwd><kwd>angiogenesis</kwd><kwd>extracellular matrix</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>макрофаг</kwd><kwd>цитокин</kwd><kwd>почечно-клеточный рак</kwd><kwd>макрофаги</kwd><kwd>ассоциированные с опухолью</kwd><kwd>ангиогенез</kwd><kwd>внеклеточный матрикс</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Российский научный фонд (проект № 14-15-00396).</funding-statement></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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