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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">oncotomsk</journal-id><journal-title-group><journal-title xml:lang="ru">Сибирский онкологический журнал</journal-title><trans-title-group xml:lang="en"><trans-title>Siberian journal of oncology</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1814-4861</issn><issn pub-type="epub">2312-3168</issn><publisher><publisher-name>Tomsk National Research Medical Сепtеr of the Russian Academy of Sciences</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.21294/1814-4861-2018-17-4-99-105</article-id><article-id custom-type="elpub" pub-id-type="custom">oncotomsk-822</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>ХИТИНАЗОПОДОБНЫЕ БЕЛКИ КАК ПЕРСПЕКТИВНЫЕ МАРКЕРЫ ПРИ ЗЛОКАЧЕСТВЕННЫХ НОВООБРАЗОВАНИЯХ</article-title><trans-title-group xml:lang="en"><trans-title>CHITINASE-LIKE PROTEINS AS PROMISING MARKERS IN CANCER PATIENTS</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-5758-7330</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Ларионова</surname><given-names>И. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Larionova</surname><given-names>I. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Россия, 634050, г. Томск, пр. Ленина, 36</p><p>Россия, 634009, г. Томск, пер. Кооперативный, 5</p><p>младший научный сотрудник лаборатории трансляционной клеточной и молекулярной биомедицины, Национальный исследовательский Томский государственный университет; аспирант, Научно-исследовательский институт онкологии, Томский национальный исследовательский медицинский центр Российской академии наук </p><p>SPIN-код: 6272-8422. Researcher ID (WOS): R-2391-2017. Author ID (Scopus): 57201182530</p></bio><bio xml:lang="en"><p>36, Lenina av., 634050-Tomsk, Russia</p><p>5, Kooperativny Street, Tomsk, Russia, 634050</p><p>Junior Researcher of Laboratory of Translational Cellular and Molecular Biomedicine, Tomsk State University; Postgraduate, Cancer Research Institute, Tomsk National Research Medical Center, Russian Academy of Sciences </p><p>Researcher ID (WOS): R-2391-2017. Author ID (Scopus): 57201182530</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-6236-6556</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Севастьянова</surname><given-names>Т. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Sevastyanova</surname><given-names>T. N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Россия, 634050, г. Томск, пр. Ленина, 36</p><p>Германия, 68167, Маннхайм, Theodor-Kutzer-Ufer, 1-3</p><p>научный сотрудник, Национальный исследовательский Томский государственный университет; аспирант, Институт Трансфузионной Медицины и Иммунологии, Медицинский факультет, Маннхайм, Университет Гейдельберга</p></bio><bio xml:lang="en"><p>36, Lenina av., 634050-Tomsk, Russia</p><p>1-3, Theodor-Kutzer-Ufer, 68167-Mannheim, Germany</p><p>Junior Researcher of Laboratory of Translational Cellular and Molecular Biomedicine, Tomsk State University; Postgraduate, Cancer Research Institute, Tomsk National Research Medical Center, Russian Academy of Sciences </p><p>Researcher ID (WOS): R-2391-2017. Author ID (Scopus): 57201182530</p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-9347-7806</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Ракина</surname><given-names>А. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Rakina</surname><given-names>A. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Россия, 634009, г. Томск, пр.Ленина, 32</p><p>инженер, Национальный исследовательский Томский политехнический университет</p><p>SPIN-код: 2569-1297. Researcher ID (WOS): O-6297-2018</p><p> </p></bio><bio xml:lang="en"><p>30, Lenina av., Tomsk, Russia, 634050</p><p>Engineer, National Research Tomsk Polytechnic University </p><p>Researcher ID (WOS): O-6297-2018.</p></bio><xref ref-type="aff" rid="aff-3"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-1526-9013</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Чердынцева</surname><given-names>Н. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Cherdyntseva</surname><given-names>N. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Россия, 634050, г. Томск, пр. Ленина, 36</p><p>Россия, 634009, г. Томск, пер. Кооперативный, 5</p><p>доктор биологических наук, профессор, член-корреспондент РАН, заведующая лабораторией молекулярной онкологии и иммунологии, Научно-исследовательский  институт онкологии, Томский национальный исследовательский медицинский центр Российской академии наук; ведущий научный сотрудник, Национальный исследовательский Томский государственный университет</p><p>SPIN-код: 5344-0990. Researcher ID (WOS): С-7943-2012. Author ID (Scopus): 6603911744</p></bio><bio xml:lang="en"><p>36, Lenina av., 634050-Tomsk, Russia</p><p>5, Kooperativny Street, Tomsk, Russia, 634050</p><p>DSс, Professor, Corresponding member of Russian Academy of Sciences, the Head of the Laboratory of Molecular oncology and immunology, Cancer Research Institute, Tomsk National Research Medical Center, Russian Academy of Sciences; senior researcher of Laboratory of translational cellular and molecular biomedicine, Tomsk State University </p><p>Researcher ID (WOS): С-7943-2012. Author ID (Scopus): 6603911744</p></bio><email xlink:type="simple">nvch@tnimc.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-0898-3075</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Кжышковска</surname><given-names>Ю. Г.</given-names></name><name name-style="western" xml:lang="en"><surname>Kzhyshkowska</surname><given-names>Ju. G.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Россия, 634050, г. Томск, пр. Ленина, 36</p><p>Германия, 68167, Маннхайм, Theodor-Kutzer-Ufer, 1-3</p><p>Германия, 68167, Маннхайм, Friedrich-Ebert, 107</p><p>доктор биологических наук, профессор, заведующая лабораторией трансляционной клеточной и молекулярной биомедицины, Национальный исследовательский Томский государственный университет; заведующая отделом врожденного иммунитета и толерантности, Институт трансфузионной медицины и иммунологии, Медицинский факультет, Университет Гейдельберга </p><p>SPIN-код: 2465-2280. Researcher ID (WOS): J-5835-2016. Author ID (Scopus): 6603091281</p></bio><bio xml:lang="en"><p>36, Lenina av., 634050-Tomsk, Russia</p><p>1-3, Theodor-Kutzer-Ufer, 68167-Mannheim, Germany</p><p>107, Friedrich-Ebert Str., 68167-Mannheim, Germany</p><p>DSс, Professor, the Head of the Laboratory of translational cellular and molecular biomedicine, Tomsk State University; Head of Department of Innate Immunity and Tolerance, Institute of Transfusion Medicine and Immunology, Medical Faculty Mannheim, University of Heidelberg </p><p>Researcher ID (WOS): J-5835-2016. Author ID (Scopus): 6603091281</p></bio><xref ref-type="aff" rid="aff-4"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Национальный исследовательский Томский государственный университет&#13;
&#13;
Научно-исследовательский институт онкологии, Томский национальный исследовательский медицинский центр Российской академии наук</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Tomsk State University&#13;
&#13;
Cancer Research Institute, Tomsk National Research Medical Center, Russian Academy of Sciences</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Национальный исследовательский Томский государственный университет&#13;
&#13;
Институт трансфузионной медицины и иммунологии, Медицинский факультет, Маннхайм, Университет Гейдельберга</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Tomsk State University&#13;
&#13;
Institute of Transfusion Medicine and Immunology, Medical Faculty Mannheim, University of Heidelberg</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-3"><aff xml:lang="ru"><institution>Национальный исследовательский Томский политехнический университет</institution><country>Россия</country></aff><aff xml:lang="en"><institution>National Research Tomsk Polytechnic University</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-4"><aff xml:lang="ru"><institution>Национальный исследовательский Томский государственный университет&#13;
&#13;
Институт трансфузионной медицины и иммунологии, Медицинский факультет, Маннхайм, Университет Гейдельберга&#13;
&#13;
Служба крови Немецкого Красного Креста Баден-Вюртемберг-Гессен</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Tomsk State University&#13;
&#13;
Institute of Transfusion Medicine and Immunology, Medical Faculty Mannheim, University of Heidelberg&#13;
&#13;
German Red Cross Blood Service Baden-Württemberg-Hessen</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2018</year></pub-date><pub-date pub-type="epub"><day>04</day><month>09</month><year>2018</year></pub-date><volume>17</volume><issue>4</issue><fpage>99</fpage><lpage>105</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Ларионова И.В., Севастьянова Т.Н., Ракина А.А., Чердынцева Н.В., Кжышковска Ю.Г., 2018</copyright-statement><copyright-year>2018</copyright-year><copyright-holder xml:lang="ru">Ларионова И.В., Севастьянова Т.Н., Ракина А.А., Чердынцева Н.В., Кжышковска Ю.Г.</copyright-holder><copyright-holder xml:lang="en">Larionova I.V., Sevastyanova T.N., Rakina A.A., Cherdyntseva N.V., Kzhyshkowska J.G.</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://www.siboncoj.ru/jour/article/view/822">https://www.siboncoj.ru/jour/article/view/822</self-uri><abstract><p>В обзоре проанализированы данные о роли хитиназоподобных белков (CLP), принадлежащих к семейству  белков, содержащих Glyco_18 домен и не обладающих ферментативной активностью, при различных  злокачественных новообразованиях. У человека идентифицировано 3 таких белка: YKL-40 (CHI3L1), YKL-39  (CHI3L2) и стабилин-связывающий CLP (SI-CLP). Хитиназоподобные белки, продуцируемые различными типами  клеток, в том числе опухолевыми, проявляют активность как цитокины и ростовые факторы, а также  они вовлечены в процессы воспаления. Высокий уровень CLP определяется в циркулирующей крови при  воспалительных заболеваниях и разных локализациях злокачественных опухолей. Освещены данные о  ключевых функциях CLP в физиологических и патологических условиях. Проанализированы сведения о  вовлечении CLP в процессы инвазии, метастазирования, ангиогенеза, их связи с опухолевой прогрессией.  Представлены собственные результаты, подтверждающие перспективность разработки прогностических и  предсказательных маркеров на основе CLP при злокачественных новообразованиях.</p></abstract><trans-abstract xml:lang="en"><p>In the present review we collected the main studies regarding the role of chitinase-like proteins (CLPs), belonging to the family of Glyco_18 domain-containing proteins, in different cancers. In  humans, 3 chitinaselike proteins have been identified: YKL-40 (CHI3L1), YKL-39 (CHI3L2) and  stabilin-1-interacting chitinase-like protein (SI-CLP). CLPs are produced by several types of cells  and combine the properties of cytokines and growth factors. The high levels of CLPs were  identified in the circulation of the patients with inflammatory diseases and various types of  tumors. We highlighted the main known functions of CLPs in normal and pathological conditions, their contribution to metastasis development, angiogenesis, invasion and other processes in  cancer, the correlation of the levels of CLPs with tumour progression. Our data also contribute to the understanding of question how CLP could be useful for cancer patient benefit.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>хитиназоподобные белки</kwd><kwd>CLP</kwd><kwd>YKL-30</kwd><kwd>YKL-40</kwd><kwd>SI-CLP</kwd><kwd>злокачественные новообразования</kwd><kwd>опухолевая прогрессия</kwd></kwd-group><kwd-group xml:lang="en"><kwd>chitinase-like proteins</kwd><kwd>CLP</kwd><kwd>YKL-30</kwd><kwd>YKL-40</kwd><kwd>SI-CLP</kwd><kwd>cancer</kwd><kwd>tumor progression</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">Kzhyshkowska J., Gratchev, A., Goerdt, S. Human chitinases and chitinase-like proteins as indicators for inflammation and cancer. Biomark Insights. 2007 May 3; 2: 128–46.</mixed-citation><mixed-citation xml:lang="en">Kzhyshkowska J., Gratchev, A., Goerdt, S. Human chitinases and chitinase-like proteins as indicators for inflammation and cancer. Biomark Insights. 2007 May 3; 2: 128–46.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Shuhui L., Mok Y.K., Wong W.S. Role of mammalian chitinases in asthma. Int Arch Allergy Immunol. 2009; 149(4): 369–77. doi: 10.1159/000205583.</mixed-citation><mixed-citation xml:lang="en">Shuhui L., Mok Y.K., Wong W.S. Role of mammalian chitinases in asthma. Int Arch Allergy Immunol. 2009; 149(4): 369–77. doi: 10.1159/000205583.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Donnelly L.E., Barnes, P.J. Acidic mammalian chitinase–a potential target for asthma therapy. Trends Pharmacol Sci. 2004 Oct; 25(10): 509–11. doi: 10.1016/j.tips.2004.08.002.</mixed-citation><mixed-citation xml:lang="en">Donnelly L.E., Barnes, P.J. Acidic mammalian chitinase–a potential target for asthma therapy. Trends Pharmacol Sci. 2004 Oct; 25(10): 509–11. doi: 10.1016/j.tips.2004.08.002.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Zhu Z., Zheng T., Homer R.J., Kim Y.-K., Chen N.Y., Cohn L., Hamid Q., Elias J.A. Acidic mammalian chitinase in asthmatic Th2 inflammation and IL-13 pathway activation. Science. 2004 Jun 11; 304(5677): 1678–82. doi: 10.1126/science.1095336.</mixed-citation><mixed-citation xml:lang="en">Zhu Z., Zheng T., Homer R.J., Kim Y.-K., Chen N.Y., Cohn L., Hamid Q., Elias J.A. Acidic mammalian chitinase in asthmatic Th2 inflammation and IL-13 pathway activation. Science. 2004 Jun 11; 304(5677): 1678–82. doi: 10.1126/science.1095336.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Boot R.G., Renkema G.H., Strijland A., van Zonneveld A.J., Aerts J.M. Cloning of a cDNA encoding chitotriosidase, a human chitinase produced by macrophages. J Biol Chem. 1995 Nov 3; 270(44): 26252–6.</mixed-citation><mixed-citation xml:lang="en">Boot R.G., Renkema G.H., Strijland A., van Zonneveld A.J., Aerts J.M. Cloning of a cDNA encoding chitotriosidase, a human chitinase produced by macrophages. J Biol Chem. 1995 Nov 3; 270(44): 26252–6.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Boven L.A., van Meurs M., Boot R.G., Mehta A., Boon L., Aerts J.M., Laman J.D. Gaucher cells demonstrate a distinct macrophage phenotype and resemble alternatively activated macrophages. Am J Clin Pathol. 2004 Sep; 122(3): 359–69. doi: 10.1309/BG5V-A8JR-DQH1-M7HN.</mixed-citation><mixed-citation xml:lang="en">Boven L.A., van Meurs M., Boot R.G., Mehta A., Boon L., Aerts J.M., Laman J.D. Gaucher cells demonstrate a distinct macrophage phenotype and resemble alternatively activated macrophages. Am J Clin Pathol. 2004 Sep; 122(3): 359–69. doi: 10.1309/BG5V-A8JR-DQH1-M7HN.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Hu B., Trinh K., Figueira W.F., Price P.A. Isolation and sequence of a novel human chondrocyte protein related to mammalian members of the chitinase protein family. J Biol Chem. 1996 Aug 9; 271(32): 19415–20.</mixed-citation><mixed-citation xml:lang="en">Hu B., Trinh K., Figueira W.F., Price P.A. Isolation and sequence of a novel human chondrocyte protein related to mammalian members of the chitinase protein family. J Biol Chem. 1996 Aug 9; 271(32): 19415–20.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Jin H.M., Copeland N.G., Gilbert D.J., Jenkins N.A., Kirkpatrick R.B., Rosenberg M. Genetic characterization of the murine Ym1 gene and identification of a cluster of highly homologous genes. Genomics. 1998 Dec 1; 54(2): 316–22. doi: 10.1006/geno.1998.5593.</mixed-citation><mixed-citation xml:lang="en">Jin H.M., Copeland N.G., Gilbert D.J., Jenkins N.A., Kirkpatrick R.B., Rosenberg M. Genetic characterization of the murine Ym1 gene and identification of a cluster of highly homologous genes. Genomics. 1998 Dec 1; 54(2): 316–22. doi: 10.1006/geno.1998.5593.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Kzhyshkowska J., Mamidi S., Gratchev A., Kremmer E., Schmuttermaier C., Krusell L., Haus G., Utikal J., Schledzewski K., Scholtze J., Goerdt S. Novel stabilin-1 interacting chitinase-like protein (SI-CLP) is up-regulated in alternatively activated macrophages and secreted via lysosomal pathway. Blood. 2006 Apr 15; 107(8): 3221– 8. doi: 10.1182/blood-2005-07-2843.</mixed-citation><mixed-citation xml:lang="en">Kzhyshkowska J., Mamidi S., Gratchev A., Kremmer E., Schmuttermaier C., Krusell L., Haus G., Utikal J., Schledzewski K., Scholtze J., Goerdt S. Novel stabilin-1 interacting chitinase-like protein (SI-CLP) is up-regulated in alternatively activated macrophages and secreted via lysosomal pathway. Blood. 2006 Apr 15; 107(8): 3221– 8. doi: 10.1182/blood-2005-07-2843.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Kzhyshkowska J., Yin S., Liu T., Riabov V., Mitrofanova I. Role of chitinase-like proteins in cancer. Biol Chem. 2016 Mar; 397(3): 231–47. doi: 10.1515/hsz-2015-0269. doi: 10.1515/hsz-2015-0269.</mixed-citation><mixed-citation xml:lang="en">Kzhyshkowska J., Yin S., Liu T., Riabov V., Mitrofanova I. Role of chitinase-like proteins in cancer. Biol Chem. 2016 Mar; 397(3): 231–47. doi: 10.1515/hsz-2015-0269. doi: 10.1515/hsz-2015-0269.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Ranok A., Wongsantichon J., Robinson R.C., Suginta W. Structural and thermodynamic insights into chitooligosaccharide binding to human cartilage chitinase 3-like protein 2 (CHI3L2 or YKL-39). J Biol Chem. 2015 Jan 30; 290(5): 2617–29. doi: 10.1074/jbc.M114.588905.</mixed-citation><mixed-citation xml:lang="en">Ranok A., Wongsantichon J., Robinson R.C., Suginta W. Structural and thermodynamic insights into chitooligosaccharide binding to human cartilage chitinase 3-like protein 2 (CHI3L2 or YKL-39). J Biol Chem. 2015 Jan 30; 290(5): 2617–29. doi: 10.1074/jbc.M114.588905.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Schimpl M., Rush C.L., Betou M., Eggleston I.M., Recklies A.D., van Aalten D.M. Human YKL-39 is a pseudo-chitinase with retained chitooligosaccharide-binding properties. Biochem J. 2012 Aug 15; 446(1): 149–57. doi: 10.1042/BJ20120377.</mixed-citation><mixed-citation xml:lang="en">Schimpl M., Rush C.L., Betou M., Eggleston I.M., Recklies A.D., van Aalten D.M. Human YKL-39 is a pseudo-chitinase with retained chitooligosaccharide-binding properties. Biochem J. 2012 Aug 15; 446(1): 149–57. doi: 10.1042/BJ20120377.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Bigg H.F., Wait R., Rowan A.D., Cawston T.E. The mammalian chitinase-like lectin, YKL-40, binds specifically to type I collagen and modulates the rate of type I collagen fibril formation. J Biol Chem. 2006 Jul 28; 281(30): 21082–95. doi: 10.1074/jbc.M601153200.</mixed-citation><mixed-citation xml:lang="en">Bigg H.F., Wait R., Rowan A.D., Cawston T.E. The mammalian chitinase-like lectin, YKL-40, binds specifically to type I collagen and modulates the rate of type I collagen fibril formation. J Biol Chem. 2006 Jul 28; 281(30): 21082–95. doi: 10.1074/jbc.M601153200.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Fusetti F., Pijning T., Kalk K.H., Bos E., Dijkstra B.W. Crystal structure and carbohydrate-binding properties of the human cartilage glycoprotein-39. J Biol Chem. 2003 Sep 26; 278(39): 37753‑60. doi: 10.1074/jbc.M303137200.</mixed-citation><mixed-citation xml:lang="en">Fusetti F., Pijning T., Kalk K.H., Bos E., Dijkstra B.W. Crystal structure and carbohydrate-binding properties of the human cartilage glycoprotein-39. J Biol Chem. 2003 Sep 26; 278(39): 37753‑60. doi: 10.1074/jbc.M303137200.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Renkema G.H., Boot R.G., Au F.L., Donker-Koopman W.E., Strijland A., Muijsers A.O., Hrebicek M., Aerts J.M. Chitotriosidase, a chitinase, and the 39-kDa human cartilage glycoprotein, a chitin-binding lectin, are homologues of family 18 glycosyl hydrolases secreted by human macrophages. Eur J Biochem. 1998 Jan 15; 251(1‑2): 504–9.</mixed-citation><mixed-citation xml:lang="en">Renkema G.H., Boot R.G., Au F.L., Donker-Koopman W.E., Strijland A., Muijsers A.O., Hrebicek M., Aerts J.M. Chitotriosidase, a chitinase, and the 39-kDa human cartilage glycoprotein, a chitin-binding lectin, are homologues of family 18 glycosyl hydrolases secreted by human macrophages. Eur J Biochem. 1998 Jan 15; 251(1‑2): 504–9.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Nishikawa K.C., Millis A.J. gp38k (CHI3L1) is a novel adhesion and migration factor for vascular cells. Exp Cell Res. 2003 Jul 1; 287(1): 79–87.</mixed-citation><mixed-citation xml:lang="en">Nishikawa K.C., Millis A.J. gp38k (CHI3L1) is a novel adhesion and migration factor for vascular cells. Exp Cell Res. 2003 Jul 1; 287(1): 79–87.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Meng G., Zhao Y., Bai X., Liu Y., Green T.J., Luo M., Zheng X. Structure of human stabilin-1 interacting chitinase-like protein (SI-CLP) reveals a saccharide-binding cleft with lower sugar-binding selectivity. J Biol Chem. 2010 Dec 17; 285(51): 39898–904. doi: 10.1074/jbc.M110.130781.</mixed-citation><mixed-citation xml:lang="en">Meng G., Zhao Y., Bai X., Liu Y., Green T.J., Luo M., Zheng X. Structure of human stabilin-1 interacting chitinase-like protein (SI-CLP) reveals a saccharide-binding cleft with lower sugar-binding selectivity. J Biol Chem. 2010 Dec 17; 285(51): 39898–904. doi: 10.1074/jbc.M110.130781.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Chang N.C., Hung S.I., Hwa K.Y., Kato I., Chen J.E., Liu C.H., Chang A.C. A macrophage protein, Ym1, transiently expressed during inflammation is a novel mammalian lectin. J Biol Chem. 2001 May 18; 276(20): 17497–506. doi: 10.1074/jbc.M010417200.</mixed-citation><mixed-citation xml:lang="en">Chang N.C., Hung S.I., Hwa K.Y., Kato I., Chen J.E., Liu C.H., Chang A.C. A macrophage protein, Ym1, transiently expressed during inflammation is a novel mammalian lectin. J Biol Chem. 2001 May 18; 276(20): 17497–506. doi: 10.1074/jbc.M010417200.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Sekine T., Masuko-Hongo K., Matsui T., Asahara H., Takigawa M., Nishioka K., Kato T. Recognition of YKL-39, a human cartilage related protein, as a target antigen in patients with rheumatoid arthritis. Ann Rheum Dis. 2001 Jan; 60(1): 49–54.</mixed-citation><mixed-citation xml:lang="en">Sekine T., Masuko-Hongo K., Matsui T., Asahara H., Takigawa M., Nishioka K., Kato T. Recognition of YKL-39, a human cartilage related protein, as a target antigen in patients with rheumatoid arthritis. Ann Rheum Dis. 2001 Jan; 60(1): 49–54.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Shao R. Secreted glycoprotein YKL-40: A potential cancer biomarker and therapeutic target. Integr Cancer Sci Therap. 2018; 5(1): 1–1. doi: 10.15761/ICST.1000268.</mixed-citation><mixed-citation xml:lang="en">Shao R. Secreted glycoprotein YKL-40: A potential cancer biomarker and therapeutic target. Integr Cancer Sci Therap. 2018; 5(1): 1–1. doi: 10.15761/ICST.1000268.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Johansen J.S. Studies on serum YKL-40 as a biomarker in diseases with inflammation, tissue remodelling, fibroses and cancer. Dan Med Bull. 2006 May; 53(2): 172–209.</mixed-citation><mixed-citation xml:lang="en">Johansen J.S. Studies on serum YKL-40 as a biomarker in diseases with inflammation, tissue remodelling, fibroses and cancer. Dan Med Bull. 2006 May; 53(2): 172–209.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Rathcke C.N., Vestergaard H. YKL-40, a new inflammatory marker with relation to insulin resistance and with a role in endothelial dysfunction and atherosclerosis. Inflamm Res. 2006 Jun; 55(6): 221‑7. doi: 10.1007/s00011-006-0076-y.</mixed-citation><mixed-citation xml:lang="en">Rathcke C.N., Vestergaard H. YKL-40, a new inflammatory marker with relation to insulin resistance and with a role in endothelial dysfunction and atherosclerosis. Inflamm Res. 2006 Jun; 55(6): 221‑7. doi: 10.1007/s00011-006-0076-y.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Johansen J.S., Jensen B.V., Roslind A., Nielsen D., Price P.A. Serum YKL-40, a new prognostic biomarker in cancer patients? Cancer Epidemiol Biomarkers Prev. 2006 Feb; 15(2): 194–202. doi: 10.1158/1055-9965.EPI-05-0011.</mixed-citation><mixed-citation xml:lang="en">Johansen J.S., Jensen B.V., Roslind A., Nielsen D., Price P.A. Serum YKL-40, a new prognostic biomarker in cancer patients? Cancer Epidemiol Biomarkers Prev. 2006 Feb; 15(2): 194–202. doi: 10.1158/1055-9965.EPI-05-0011.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Suzuki T., Hashimoto S., Toyoda N., Nagai S., Yamazaki N., Dong H.Y., Sakai J., Yamashita T., Nukiwa T., Matsushima K. Comprehensive gene expression profile of LPS-stimulated human monocytes by SAGE. Blood 2000; 96: 2584–91.</mixed-citation><mixed-citation xml:lang="en">Suzuki T., Hashimoto S., Toyoda N., Nagai S., Yamazaki N., Dong H.Y., Sakai J., Yamashita T., Nukiwa T., Matsushima K. Comprehensive gene expression profile of LPS-stimulated human monocytes by SAGE. Blood 2000; 96: 2584–91.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Liu T., Larionova I., Litviakov N., Riabov V., Zavyalova M., Tsyganov M., Buldakov M., Song B., Moganti K., Kazantseva P., Slonimskaya E., Kremmer E., Flatley A., Klüter H., Cherdyntseva N., Kzhyshkowska J. Tumor-associated macrophages in human breast cancer produce new monocyte attracting and pro-angiogenic factor YKL-39 indicative for increased metastasis after neoadjuvant chemotherapy. Oncoimmunology. 2018 Mar 13; 7(6): e1436922. doi: 10.1080/2162402X.2018.1436922</mixed-citation><mixed-citation xml:lang="en">Liu T., Larionova I., Litviakov N., Riabov V., Zavyalova M., Tsyganov M., Buldakov M., Song B., Moganti K., Kazantseva P., Slonimskaya E., Kremmer E., Flatley A., Klüter H., Cherdyntseva N., Kzhyshkowska J. Tumor-associated macrophages in human breast cancer produce new monocyte attracting and pro-angiogenic factor YKL-39 indicative for increased metastasis after neoadjuvant chemotherapy. Oncoimmunology. 2018 Mar 13; 7(6): e1436922. doi: 10.1080/2162402X.2018.1436922</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Shao R., Hamel K., Petersen L., Cao Q.J., Arenas R.B., Bigelow C., Bentley B., Yan W. YKL-40, a secreted glycoprotein, promotes tumor angiogenesis. Oncogene. 2009 Dec 17; 28(50): 4456–68. doi: 10.1038/onc.2009.292.</mixed-citation><mixed-citation xml:lang="en">Shao R., Hamel K., Petersen L., Cao Q.J., Arenas R.B., Bigelow C., Bentley B., Yan W. YKL-40, a secreted glycoprotein, promotes tumor angiogenesis. Oncogene. 2009 Dec 17; 28(50): 4456–68. doi: 10.1038/onc.2009.292.</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Francescone R.A., Scully S., Faibish M., Taylor S.L., Oh D., Moral L., Yan W., Bentley B., Shao R. Role of YKL-40 in the angiogenesis, radioresistance, and progression of glioblastoma. J Biol Chem. 2011 Apr 29; 286(17): 15332–43. doi: 10.1074/jbc.M110.212514.</mixed-citation><mixed-citation xml:lang="en">Francescone R.A., Scully S., Faibish M., Taylor S.L., Oh D., Moral L., Yan W., Bentley B., Shao R. Role of YKL-40 in the angiogenesis, radioresistance, and progression of glioblastoma. J Biol Chem. 2011 Apr 29; 286(17): 15332–43. doi: 10.1074/jbc.M110.212514.</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Faibish M., Francescone R., Bentley B., Yan W., Shao R. A YKL-40-neutralizing antibody blocks tumor angiogenesis and progression: a potential therapeutic agent in cancers. Mol Cancer Ther. 2011; 10: 742–51. doi: 10.1158/1535-7163.MCT-10-0868.</mixed-citation><mixed-citation xml:lang="en">Faibish M., Francescone R., Bentley B., Yan W., Shao R. A YKL-40-neutralizing antibody blocks tumor angiogenesis and progression: a potential therapeutic agent in cancers. Mol Cancer Ther. 2011; 10: 742–51. doi: 10.1158/1535-7163.MCT-10-0868.</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Salamon J., Hoffmann T., Elies E., Peldschus K., Johansen J.S., Lüers G., Schumacher U., Wicklein D. Antibody directed against human YKL-40 increases tumor volume in a human melanoma xenograft model in scid mice. PLoS One. 2014 Apr 21; 9(4): e95822. doi: 10.1371/journal.pone.0095822.</mixed-citation><mixed-citation xml:lang="en">Salamon J., Hoffmann T., Elies E., Peldschus K., Johansen J.S., Lüers G., Schumacher U., Wicklein D. Antibody directed against human YKL-40 increases tumor volume in a human melanoma xenograft model in scid mice. PLoS One. 2014 Apr 21; 9(4): e95822. doi: 10.1371/journal.pone.0095822.</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Wan G., Xiang L., Sun X., Wang X., Li H., Ge W., Cao F. Elevated YKL-40 expression is associated with a poor prognosis in breast cancer patients. Oncotarget. 2017 Jan 17; 8(3): 5382–5391. doi: 10.18632/oncotarget.14280.</mixed-citation><mixed-citation xml:lang="en">Wan G., Xiang L., Sun X., Wang X., Li H., Ge W., Cao F. Elevated YKL-40 expression is associated with a poor prognosis in breast cancer patients. Oncotarget. 2017 Jan 17; 8(3): 5382–5391. doi: 10.18632/oncotarget.14280.</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Saidi A., Javerzat S., Bellahcène A., De Vos J., Bello L., Castronovo V., Deprez M., Loiseau H., Bikfalvi A., Hagedorn M. Experimental antiangiogenesis causes upregulation of genes associated with poor survival in glioblastoma. Int J Cancer. 2008 May 15; 122(10): 2187‑98. doi: 10.1002/ijc.23313.</mixed-citation><mixed-citation xml:lang="en">Saidi A., Javerzat S., Bellahcène A., De Vos J., Bello L., Castronovo V., Deprez M., Loiseau H., Bikfalvi A., Hagedorn M. Experimental antiangiogenesis causes upregulation of genes associated with poor survival in glioblastoma. Int J Cancer. 2008 May 15; 122(10): 2187‑98. doi: 10.1002/ijc.23313.</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Nio J., Fujimoto W., Konno A., Kon Y., Owhashi M., Iwanaga T. Cellular expression of murine Ym1 and Ym2, chitinase family proteins, as revealed by in situ hybridization and immunohistochemistry. Histochem Cell Biol. 2004 Jun; 121(6): 473–82. doi: 10.1007/s00418-004-0654-4.</mixed-citation><mixed-citation xml:lang="en">Nio J., Fujimoto W., Konno A., Kon Y., Owhashi M., Iwanaga T. Cellular expression of murine Ym1 and Ym2, chitinase family proteins, as revealed by in situ hybridization and immunohistochemistry. Histochem Cell Biol. 2004 Jun; 121(6): 473–82. doi: 10.1007/s00418-004-0654-4.</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Kawada M., Seno H., Kanda K., Nakanishi Y., Akitake R., Komekado H., Kawada K., Sakai Y., Mizoguchi E., Chiba T. Chitinase 3-like 1 promotes macrophage recruitment and angiogenesis in colorectal cancer. Oncogene. 2012 Jun 28; 31(26): 3111–23. doi: 10.1038/onc.2011.498.</mixed-citation><mixed-citation xml:lang="en">Kawada M., Seno H., Kanda K., Nakanishi Y., Akitake R., Komekado H., Kawada K., Sakai Y., Mizoguchi E., Chiba T. Chitinase 3-like 1 promotes macrophage recruitment and angiogenesis in colorectal cancer. Oncogene. 2012 Jun 28; 31(26): 3111–23. doi: 10.1038/onc.2011.498.</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Tang H., Sun Y., Shi Z., Huang H., Fang Z., Chen J., Xiu Q., Li B. YKL-40 induces IL-8 expression from bronchial epithelium via MAPK (JNK and ERK) and NF-κB pathways, causing bronchial smooth muscle proliferation and migration. J Immunol. 2013 Jan 1; 190(1): 438–46. doi: 10.4049/jimmunol.1201827.</mixed-citation><mixed-citation xml:lang="en">Tang H., Sun Y., Shi Z., Huang H., Fang Z., Chen J., Xiu Q., Li B. YKL-40 induces IL-8 expression from bronchial epithelium via MAPK (JNK and ERK) and NF-κB pathways, causing bronchial smooth muscle proliferation and migration. J Immunol. 2013 Jan 1; 190(1): 438–46. doi: 10.4049/jimmunol.1201827.</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Jefri M., Huang Y.N., Huang W.C., Tai C.S., Chen W.L. YKL-40 regulated epithelial- mesenchymal transition and migration/invasion enhancement in non-small cell lung cancer. BMC Cancer. 2015 Aug 15; 15: 590. doi: 10.1186/s12885-015-1592-3.</mixed-citation><mixed-citation xml:lang="en">Jefri M., Huang Y.N., Huang W.C., Tai C.S., Chen W.L. YKL-40 regulated epithelial- mesenchymal transition and migration/invasion enhancement in non-small cell lung cancer. BMC Cancer. 2015 Aug 15; 15: 590. doi: 10.1186/s12885-015-1592-3.</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Schultz N.A., Johansen J.S. YKL-40-A Protein in the Field of Translational Medicine: A Role as a Biomarker in Cancer Patients? Cancers (Basel). 2010 Jul 12; 2(3): 1453‑91. doi: 10.3390/cancers2031453.</mixed-citation><mixed-citation xml:lang="en">Schultz N.A., Johansen J.S. YKL-40-A Protein in the Field of Translational Medicine: A Role as a Biomarker in Cancer Patients? Cancers (Basel). 2010 Jul 12; 2(3): 1453‑91. doi: 10.3390/cancers2031453.</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Shao R., Cao Q.J., Arenas R.B., Bigelow C., Bentley B., Yan W. Breast cancer expression of YKL-40 correlates with tumour grade, poor differentiation, and other cancer markers. Br J Cancer. 2011 Oct 11; 105(8): 1203–9. doi: 10.1038/bjc.2011.347.</mixed-citation><mixed-citation xml:lang="en">Shao R., Cao Q.J., Arenas R.B., Bigelow C., Bentley B., Yan W. Breast cancer expression of YKL-40 correlates with tumour grade, poor differentiation, and other cancer markers. Br J Cancer. 2011 Oct 11; 105(8): 1203–9. doi: 10.1038/bjc.2011.347.</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Litviakov N., Tsyganov M., Larionova I., Ibragimova M., Deryusheva I., Kazantseva P., Slonimskaya E., Frolova I., Choinzonov E., Cherdyntseva N., Kzhyshkowska J. Expression of M2 macrophage markers YKL-39 and CCL18 in breast cancer is associated with the effect of neoadjuvant chemotherapy. Cancer Chemother Pharmacol. 2018 Jul; 82(1): 99–109. doi: 10.1007/s00280-018-3594-8.</mixed-citation><mixed-citation xml:lang="en">Litviakov N., Tsyganov M., Larionova I., Ibragimova M., Deryusheva I., Kazantseva P., Slonimskaya E., Frolova I., Choinzonov E., Cherdyntseva N., Kzhyshkowska J. Expression of M2 macrophage markers YKL-39 and CCL18 in breast cancer is associated with the effect of neoadjuvant chemotherapy. Cancer Chemother Pharmacol. 2018 Jul; 82(1): 99–109. doi: 10.1007/s00280-018-3594-8.</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Kavsan V.M., Baklaushev V.P., Balynska O.V., Iershov A.V., Areshkov P.O., Yusubalieva G.M., Grinenko N.P., Victorov I.V., Rymar V.I., Sanson M., Chekhonin V.P. Gene Encoding Chitinase 3-Like 1 Protein (CHI3L1) is a Putative Oncogene. Int J Biomed Sci. 2011 Sep; 7(3): 230–7.</mixed-citation><mixed-citation xml:lang="en">Kavsan V.M., Baklaushev V.P., Balynska O.V., Iershov A.V., Areshkov P.O., Yusubalieva G.M., Grinenko N.P., Victorov I.V., Rymar V.I., Sanson M., Chekhonin V.P. Gene Encoding Chitinase 3-Like 1 Protein (CHI3L1) is a Putative Oncogene. Int J Biomed Sci. 2011 Sep; 7(3): 230–7.</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Itik V., Kemik O., Kemik A., Dulger A.C., Sümer A., Soyoral Y.U., Begenik H., Purisa S., Kotan C. Serum YKL-40 Levels in Patients with Gastric Cancer. Biomark Cancer. 2011 May 4; 3: 25–30. doi: 10.4137/BIC.S7154.</mixed-citation><mixed-citation xml:lang="en">Itik V., Kemik O., Kemik A., Dulger A.C., Sümer A., Soyoral Y.U., Begenik H., Purisa S., Kotan C. Serum YKL-40 Levels in Patients with Gastric Cancer. Biomark Cancer. 2011 May 4; 3: 25–30. doi: 10.4137/BIC.S7154.</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Dupont J., Tanwar M.K., Thaler H.T., Fleisher M., Kauff N., Hensley M.L., Sabbatini P., Anderson S., Aghajanian C., Holland E.C., Spriggs D.R. Early detection and prognosis of ovarian cancer using serum YKL-40. J Clin Oncol 2004; 22: 3330–9. doi: 10.1200/JCO.2004.09.112.</mixed-citation><mixed-citation xml:lang="en">Dupont J., Tanwar M.K., Thaler H.T., Fleisher M., Kauff N., Hensley M.L., Sabbatini P., Anderson S., Aghajanian C., Holland E.C., Spriggs D.R. Early detection and prognosis of ovarian cancer using serum YKL-40. J Clin Oncol 2004; 22: 3330–9. doi: 10.1200/JCO.2004.09.112.</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Yasar O., Akcay T., Obek C., Turegun F.A. Diagnostic potential of YKL-40 in bladder cancer. Urol Oncol. 2016 Jun; 34(6): 257.e19‑24. doi: 10.1016/j.urolonc.2016.02.003.</mixed-citation><mixed-citation xml:lang="en">Yasar O., Akcay T., Obek C., Turegun F.A. Diagnostic potential of YKL-40 in bladder cancer. Urol Oncol. 2016 Jun; 34(6): 257.e19‑24. doi: 10.1016/j.urolonc.2016.02.003.</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Bi J., Lau S.H., Lv Z.L., Xie D., Li W., Lai Y.R., Zhong J.M., Wu H.Q., Su Q., He Y.L., Zhan W.H., Wen J.M., Guan X.Y. Overexpression of YKL-40 is an independent prognostic marker in gastric cancer. Hum Pathol. 2009 Dec; 40(12): 1790–7. doi: 10.1016/j.humpath.2009.07.005.</mixed-citation><mixed-citation xml:lang="en">Bi J., Lau S.H., Lv Z.L., Xie D., Li W., Lai Y.R., Zhong J.M., Wu H.Q., Su Q., He Y.L., Zhan W.H., Wen J.M., Guan X.Y. Overexpression of YKL-40 is an independent prognostic marker in gastric cancer. Hum Pathol. 2009 Dec; 40(12): 1790–7. doi: 10.1016/j.humpath.2009.07.005.</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">Johansen J.S., Drivsholm L., Price P.A., Christensen I.J. High serum YKL-40 level in patients with small cell lung cancer is related to early death. Lung Cancer. 2004; 46: 333–340. doi: 10.1016/j.lungcan.2004.05.010.</mixed-citation><mixed-citation xml:lang="en">Johansen J.S., Drivsholm L., Price P.A., Christensen I.J. High serum YKL-40 level in patients with small cell lung cancer is related to early death. Lung Cancer. 2004; 46: 333–340. doi: 10.1016/j.lungcan.2004.05.010.</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">Cintin C., Johansen J.S., Christensen I.J., Price P.A., Sørensen S., Nielsen H.J. High serum YKL-40 level after surgery for colorectal carcinoma is related to short survival. Cancer. 2002; 95: 267–274. doi: 10.1002/cncr.10644.</mixed-citation><mixed-citation xml:lang="en">Cintin C., Johansen J.S., Christensen I.J., Price P.A., Sørensen S., Nielsen H.J. High serum YKL-40 level after surgery for colorectal carcinoma is related to short survival. Cancer. 2002; 95: 267–274. doi: 10.1002/cncr.10644.</mixed-citation></citation-alternatives></ref><ref id="cit46"><label>46</label><citation-alternatives><mixed-citation xml:lang="ru">Johansen J.S., Bojesen S.E., Mylin A.K., Frikke-Schmidt R., Price P.A., Nordestgaard B.G. Elevated plasma YKL-40 predicts increased risk of gastrointestinal cancer and decreased survival after any cancer diagnosis in the general population. J Clin Oncol. 2009 Feb 1; 27(4): 572–8. doi: 10.1200/JCO.2008.18.8367.</mixed-citation><mixed-citation xml:lang="en">Johansen J.S., Bojesen S.E., Mylin A.K., Frikke-Schmidt R., Price P.A., Nordestgaard B.G. Elevated plasma YKL-40 predicts increased risk of gastrointestinal cancer and decreased survival after any cancer diagnosis in the general population. J Clin Oncol. 2009 Feb 1; 27(4): 572–8. doi: 10.1200/JCO.2008.18.8367.</mixed-citation></citation-alternatives></ref><ref id="cit47"><label>47</label><citation-alternatives><mixed-citation xml:lang="ru">Chang S.T., Zahn J.M., Horecka J., Kunz P.L., Ford J.M., Fisher G.A., Le Q.T., Chang D.T., Ji H., Koong A.C. Identification of a biomarker panel using a multiplex proximity ligation assay improves accuracy of pancreatic cancer diagnosis. J Transl Med. 2009 Dec 11; 7: 105. doi: 10.1186/1479-5876-7-105.</mixed-citation><mixed-citation xml:lang="en">Chang S.T., Zahn J.M., Horecka J., Kunz P.L., Ford J.M., Fisher G.A., Le Q.T., Chang D.T., Ji H., Koong A.C. Identification of a biomarker panel using a multiplex proximity ligation assay improves accuracy of pancreatic cancer diagnosis. J Transl Med. 2009 Dec 11; 7: 105. doi: 10.1186/1479-5876-7-105.</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
