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<article article-type="research-article" dtd-version="1.3" 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" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">vestib</journal-id><journal-title-group><journal-title xml:lang="ru">Известия Национальной  академии наук Беларуси. Серия биологических наук</journal-title><trans-title-group xml:lang="en"><trans-title>Proceedings of the National Academy of Sciences of Belarus, Biological Series</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1029-8940</issn><issn pub-type="epub">2524-230X</issn><publisher><publisher-name>The Republican Unitary Enterprise Publishing House "Belaruskaya Navuka"</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">vestib-264</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ОБЗОРЫ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>REVIEWS</subject></subj-group></article-categories><title-group><article-title>АДЕНОЗИН КАК ПОТЕНЦИАЛЬНАЯ МИШЕНЬ ДЛЯ БИОТЕРАПИИ РАКА</article-title><trans-title-group xml:lang="en"><trans-title>ADENOSINE AS A POTENTIAL TARGET FOR CANCER BIOTHERAPY</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Зинченко</surname><given-names>А. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Zinchenko</surname><given-names>A. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>д-р биол. наук, проф., зав. лабораторией Института</p></bio><bio xml:lang="en"><p>D. Sc. (Biol.), Professor, Head of Laboratory</p></bio><email xlink:type="simple">zinch@mbio.bas-net.by</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Институт микробиологии НАН Беларуси</institution><country>Беларусь</country></aff><aff xml:lang="en"><institution>Institute of Microbiology of the National Academy of Sciences of Belarus</institution><country>Belarus</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2016</year></pub-date><pub-date pub-type="epub"><day>17</day><month>11</month><year>2016</year></pub-date><volume>0</volume><issue>4</issue><fpage>118</fpage><lpage>128</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Зинченко А.И., 2016</copyright-statement><copyright-year>2016</copyright-year><copyright-holder xml:lang="ru">Зинченко А.И.</copyright-holder><copyright-holder xml:lang="en">Zinchenko A.I.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://vestibio.belnauka.by/jour/article/view/264">https://vestibio.belnauka.by/jour/article/view/264</self-uri><abstract><p>В данном обзоре литературы расссматривается роль внеклеточного аденозина в формировании иммуносупрессивного аденозинергического микроокружения солидных опухолей. Вызванное гипоксией накопление внеклеточного аденозина в концентрации 50– 100 мкМ (норма 10–100 нМ) является патофизиологическим признаком широкого круга злокачественных новообразований у человека. У аденозина как сигнальной молекулы выявлено четыре типа поверхностно-клеточных рецепторов, активация которых приводит к ингибированию эффекторных функций цитотоксических Т-лимфоцитов, натуральных киллеров и макрофагов, играющих ключевую роль в противоопухолевых иммунных ответах. Автором предложена идея устранения защиты рака от иммунитета с помощью денозиндезаминазы, слитой с аннексином-А5. По мнению автора, такой химерный белок при введении в организм пациентов, страдающих от онкологических заболеваний, будет связываться только с раковыми клетками и разрушать аденозин, защищающий эти клетки от противоопухолевого иммунитета.</p></abstract><trans-abstract xml:lang="en"><p>The literature review describes the role of extracellular adenosine in formation of immunosuppressive adenosinergic microenvironment of solid tumors. Hypoxia-induced accumulation of extracellular adenosine in 50–100 μM concentration (cf the normal 10–100 nM) is a pathophysiological indicator of a broad spectrum of human malignant neoplastic diseases. Four types of cell surface receptors for adenosine as the signal molecule have been revealed. Upon activation the receptors cause inhibition of effector functions of cytotoxic T-lymphocytes, native killers and macrophages playing a key part in antitumor immune response. The author of the review proposed the idea to remove the procancer shield from immune attack using adenosine deaminase fused with annexin A5. It was postulated that such chimeric protein injected into the body of cancer patient will bind exclusively with tumor cells and disrupt adenosine protecting them from cancerostatic immune action. </p></trans-abstract><kwd-group xml:lang="ru"><kwd>внеклеточный аденозин</kwd><kwd>аденозиновые рецепторы</kwd><kwd>опухолевое микроокружение</kwd><kwd>иммуносу- прессия</kwd><kwd>биотерапия рака</kwd><kwd>аденозиндезаминаза</kwd><kwd>аннексин-А5</kwd></kwd-group><kwd-group xml:lang="en"><kwd>extracellular adenosine</kwd><kwd>adenosine receptors</kwd><kwd>tumor microenvironment</kwd><kwd>immunosupression</kwd><kwd>cancer biotherapy</kwd><kwd>adenosine deaminase</kwd><kwd>annexin A5</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Blay, J. 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