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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">171</article-id><article-id pub-id-type="doi">10.17650/2313-805X-2018-5-4-20-28</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">Tumor associated macrophages: current research and perspectives of clinical use</article-title><trans-title-group xml:lang="ru"><trans-title>Макрофаги, ассоциированные с опухолью: современное состояние исследований и перспективы клинического использования</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-2137-1866</contrib-id><name-alternatives><name xml:lang="en"><surname>Gratchev</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 contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-5639-0835</contrib-id><name-alternatives><name xml:lang="en"><surname>Samoilova</surname><given-names>D. V.</given-names></name><name xml:lang="ru"><surname>Самойлова</surname><given-names>Д. 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>Rashidova</surname><given-names>M. A.</given-names></name><name xml:lang="ru"><surname>Рашидова</surname><given-names>М. А.</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"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-6951-3996</contrib-id><name-alternatives><name xml:lang="en"><surname>Petrenko</surname><given-names>A. A.</given-names></name><name xml:lang="ru"><surname>Петренко</surname><given-names>А. А.</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"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-6132-9924</contrib-id><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-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Research Institute of Carcinogenesis, N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia</institution></aff><aff><institution xml:lang="ru">НИИ канцерогенеза, ФГБУ «Национальный медицинский исследовательский центр онкологии им. Н.Н. Блохина»  Минздрава России</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2018-12-15" publication-format="electronic"><day>15</day><month>12</month><year>2018</year></pub-date><volume>5</volume><issue>4</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>20</fpage><lpage>28</lpage><history><date date-type="received" iso-8601-date="2019-01-03"><day>03</day><month>01</month><year>2019</year></date><date date-type="accepted" iso-8601-date="2019-01-03"><day>03</day><month>01</month><year>2019</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2018, Gratchev A.N., Samoilova D.V., Rashidova M.A., Petrenko A.A., Kovaleva O.V.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2018, Грачев А.Н., Самойлова Д.В., Рашидова М.А., Петренко А.А., Ковалева О.В.</copyright-statement><copyright-year>2018</copyright-year><copyright-holder xml:lang="en">Gratchev A.N., Samoilova D.V., Rashidova M.A., Petrenko A.A., Kovaleva O.V.</copyright-holder><copyright-holder xml:lang="ru">Грачев А.Н., Самойлова Д.В., Рашидова М.А., Петренко А.А., Ковалева О.В.</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/171">https://umo.abvpress.ru/jour/article/view/171</self-uri><abstract xml:lang="en"><p>Macrophages are the key cells of the innate immune system. One of the main functions of macrophages is the regulation of inflammation. Being common in all tissues and organs of the human body, tissue macrophages control their condition and guarantee a timely and effective response to damage, pathogen penetration or cell transformation. After eliminating the cause of inflammation, macrophages initiate the processes of healing and restoration of tissue homeostasis. At the end of the 20<sup>th</sup> century, the concept of macrophage activation dichotomy was proposed, which divided them into classically (M1) and alternatively (M2) activated ones. The development of this concept has led to the description of a wide variety of macrophage phenotypes. At the same time, M2 continues to be considered a prototype of tumor associated macrophages (TAM).</p><p>TAM represent one of the most important cell types in the tumor microenvironment. Like all macrophages, they have a certain level of heterogeneity and plasticity, which develop under the influence of cytokines and growth factors produced by tumor cells. TAM, in turn, produces growth factors, cytokines and extracellular matrix components that support the progression of the tumor and increase its malignant potential. Numerous clinical studies have shown that the amount of TAM is often correlated with a poor prognosis of the disease. TAM perform a large number of functions necessary to maintain tumor progression. They are capable of stimulating angiogenesis and reorganization of the vascular system. Since the role of TAM in tumor development has become apparent, various attempts have been made to use them in the clinic.  It can be confidently asserted that various TAM markers are very attractive as diagnostic and prognostic markers of various tumors, and also as promising targets for the development of new targeted therapeutic agents.</p></abstract><trans-abstract xml:lang="ru"><p/></trans-abstract><kwd-group xml:lang="en"><kwd>macrophage</kwd><kwd>cancer</kwd><kwd>tumor associated macrophage</kwd><kwd>inflammation</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>макрофаг</kwd><kwd>рак</kwd><kwd>опухолеассоциированный макрофаг</kwd><kwd>воспаление</kwd></kwd-group><funding-group><funding-statement xml:lang="en">Russian Foundation for Basic Research, grant Nо 17-04-01857</funding-statement><funding-statement xml:lang="ru">Российский фонд фундаментальных исследований, научный проект № 17-04-01857</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. Fernandez-Velasco M., Gonzalez-Ra- mos S., Bosca L. Involvement of monocytes/macrophages as key factors in the development and progression of cardiovascular diseases. Biochem J 2014;458(2):187–93. DOI: 10.1042/BJ20131501. PMID: 24524191.</mixed-citation><mixed-citation xml:lang="ru">Fernandez-Velasco M., Gonzalez-Ra- mos S., Bosca L. Involvement of monocytes/macrophages as key factors in the development and progression of cardiovascular diseases. Biochem J 2014;458(2):187–93. DOI: 10.1042/BJ20131501. PMID: 24524191.</mixed-citation></citation-alternatives></ref><ref id="B2"><label>2.</label><citation-alternatives><mixed-citation xml:lang="en">2. Chavez-Sanchez L., Espinosa-Luna J.E., Chavez-Rueda K. et al. Innate immune system cells in atherosclerosis. Arch Med Res 2014;45(1):1–14. DOI: 10.1016/j.arcmed.2013.11.007. PMID: 24326322.</mixed-citation><mixed-citation xml:lang="ru">Chavez-Sanchez L., Espinosa-Luna J.E., Chavez-Rueda K. et al. Innate immune system cells in atherosclerosis. Arch Med Res 2014;45(1):1–14. DOI: 10.1016/j.arcmed.2013.11.007. PMID: 24326322.</mixed-citation></citation-alternatives></ref><ref id="B3"><label>3.</label><citation-alternatives><mixed-citation xml:lang="en">3. Gordon S., Taylor P.R. Monocyte and macrophage heterogeneity. Nat Rev Immunol 2005;5(12):953–64. DOI: 10.1038/ nri1733. PMID: 16322748.</mixed-citation><mixed-citation xml:lang="ru">Gordon S., Taylor P.R. Monocyte and macrophage heterogeneity. Nat Rev Immunol 2005;5(12):953–64. DOI: 10.1038/ nri1733. PMID: 16322748.</mixed-citation></citation-alternatives></ref><ref id="B4"><label>4.</label><citation-alternatives><mixed-citation xml:lang="en">4. Gratchev A., Kzhyshkowska J., Kothe K. et al. Mphi1 and Mphi2 can be re-polarized by Th2 or Th1 cytokines, respectively, and respond to exogenous danger signals. Immunobiology 2006;211(6–8):473–86. DOI: 10.1016/j.imbio.2006.05.017. PMID: 16920487.</mixed-citation><mixed-citation xml:lang="ru">Gratchev A., Kzhyshkowska J., Kothe K. et al. Mphi1 and Mphi2 can be re-polarized by Th2 or Th1 cytokines, respectively, and respond to exogenous danger signals. Immunobiology 2006;211(6–8):473–86. DOI: 10.1016/j.imbio.2006.05.017. PMID: 16920487.</mixed-citation></citation-alternatives></ref><ref id="B5"><label>5.</label><citation-alternatives><mixed-citation xml:lang="en">5. Hansson G.K. Inflammation, atherosclerosis, and coronary artery disease. N Engl J Med 2005;352(16):1685–95. DOI: 10.1056/NEJMra043430. PMID: 15843671.</mixed-citation><mixed-citation xml:lang="ru">Hansson G.K. Inflammation, atherosclerosis, and coronary artery disease. N Engl J Med 2005;352(16):1685–95. DOI: 10.1056/NEJMra043430. PMID: 15843671.</mixed-citation></citation-alternatives></ref><ref id="B6"><label>6.</label><citation-alternatives><mixed-citation xml:lang="en">6. Bingle L., Brown N.J., Lewis C.E. The role of tumour-associated macrophages in tumour progression: implications for new anticancer therapies. J Pathol 2002;196(3):254–65. DOI: 10.1002/path.1027. PMID: 11857487.</mixed-citation><mixed-citation xml:lang="ru">Bingle L., Brown N.J., Lewis C.E. The role of tumour-associated macrophages in tumour progression: implications for new anticancer therapies. J Pathol 2002;196(3):254–65. DOI: 10.1002/path.1027. PMID: 11857487.</mixed-citation></citation-alternatives></ref><ref id="B7"><label>7.</label><citation-alternatives><mixed-citation xml:lang="en">7. Stout R.D., Suttles J. Functional plasticity of macrophages: reversible adaptation to changing microenvironments. J Leukoc Biol 2004;76(3):509–13. DOI: 10.1189/jlb.0504272. PMID: PMC1201486.</mixed-citation><mixed-citation xml:lang="ru">Stout R.D., Suttles J. Functional plasticity of macrophages: reversible adaptation to changing microenvironments. J Leukoc Biol 2004;76(3):509–13. DOI: 10.1189/jlb.0504272. PMID: PMC1201486.</mixed-citation></citation-alternatives></ref><ref id="B8"><label>8.</label><citation-alternatives><mixed-citation xml:lang="en">8. Stein M., Keshav S., Harris N., Gordon S. Interleukin 4 potently enhances murine macrophage mannose receptor activity: a marker of alternative immunologic macrophage activation. J Exp Med 1992;176(1):287–92. PMID: 1613462.</mixed-citation><mixed-citation xml:lang="ru">Stein M., Keshav S., Harris N., Gordon S. Interleukin 4 potently enhances murine macrophage mannose receptor activity: a marker of alternative immunologic macrophage activation. J Exp Med 1992;176(1):287–92. PMID: 1613462.</mixed-citation></citation-alternatives></ref><ref id="B9"><label>9.</label><citation-alternatives><mixed-citation xml:lang="en">9. Locati M., Mantovani A., Sica A. Macrophage activation and polarization as an adaptive component of innate immunity. Adv Immunol 2013;120:163–84. DOI: 10.1016/B978-0-12-4170285.00006-5. PMID: 24070384.</mixed-citation><mixed-citation xml:lang="ru">Locati M., Mantovani A., Sica A. Macrophage activation and polarization as an adaptive component of innate immunity. Adv Immunol 2013;120:163–84. DOI: 10.1016/B978-0-12-4170285.00006-5. PMID: 24070384.</mixed-citation></citation-alternatives></ref><ref id="B10"><label>10.</label><citation-alternatives><mixed-citation xml:lang="en">10. Gratchev A., Schledzewski K., Guillot P., Goerdt S. Alternatively activated antigenpresenting cells: molecular repertoire, immune regulation, and healing. Skin Pharmacol Appl Skin Physiol 2001;14(5):272–9. DOI: 10.1159/000056357. PMID: 11586068.</mixed-citation><mixed-citation xml:lang="ru">Gratchev A., Schledzewski K., Guillot P., Goerdt S. Alternatively activated antigenpresenting cells: molecular repertoire, immune regulation, and healing. Skin Pharmacol Appl Skin Physiol 2001;14(5):272–9. DOI: 10.1159/000056357. PMID: 11586068.</mixed-citation></citation-alternatives></ref><ref id="B11"><label>11.</label><citation-alternatives><mixed-citation xml:lang="en">11. Mantovani A. Chemokines in neoplastic progression. Semin Cancer Biol 2004;14(3):147–8. DOI: 10.1016/j.semcancer.2003.10.010. PMID: 15246048.</mixed-citation><mixed-citation xml:lang="ru">Mantovani A. Chemokines in neoplastic progression. Semin Cancer Biol 2004;14(3):147–8. DOI: 10.1016/j.semcancer.2003.10.010. PMID: 15246048.</mixed-citation></citation-alternatives></ref><ref id="B12"><label>12.</label><citation-alternatives><mixed-citation xml:lang="en">12. Ferreira M.A. Cytokine expression in allergic inflammation: systematic review of in vivo challenge studies. Mediators Inflamm 2003;12(5):259–67. DOI: 10.1080/09629350310001619717. PMID: 14760932.</mixed-citation><mixed-citation xml:lang="ru">Ferreira M.A. Cytokine expression in allergic inflammation: systematic review of in vivo challenge studies. Mediators Inflamm 2003;12(5):259–67. DOI: 10.1080/09629350310001619717. PMID: 14760932.</mixed-citation></citation-alternatives></ref><ref id="B13"><label>13.</label><citation-alternatives><mixed-citation xml:lang="en">13. Goerdt S., Politz O., Schledzewski K. et al. Alternative versus classical activation of macrophages. Pathobiology 1999; 67(5–6):222–6. DOI: 10.1159/000028096. PMID: 10725788.</mixed-citation><mixed-citation xml:lang="ru">Goerdt S., Politz O., Schledzewski K. et al. Alternative versus classical activation of macrophages. Pathobiology 1999; 67(5–6):222–6. DOI: 10.1159/000028096. PMID: 10725788.</mixed-citation></citation-alternatives></ref><ref id="B14"><label>14.</label><citation-alternatives><mixed-citation xml:lang="en">14. Gordon S., Clarke S., Greaves D. et al. Molecular immunobiology of macrophages: recent progress. Curr Opin Immunol 1995;7(1):24–33. PMID: 7772278.</mixed-citation><mixed-citation xml:lang="ru">Gordon S., Clarke S., Greaves D. et al. Molecular immunobiology of macrophages: recent progress. Curr Opin Immunol 1995;7(1):24–33. PMID: 7772278.</mixed-citation></citation-alternatives></ref><ref id="B15"><label>15.</label><citation-alternatives><mixed-citation xml:lang="en">15. Gratchev A., Kzhyshkowska J., Utikal J., Goerdt S. Interleukin-4 and dexamethasone counterregulate extracellular matrix remodelling and phagocytosis in type-2 macrophages. Scand J Immunol 2005;61(1):10–7. DOI: 10.1111/j.0300-9475.2005.01524.x. PMID: 15644118.</mixed-citation><mixed-citation xml:lang="ru">Gratchev A., Kzhyshkowska J., Utikal J., Goerdt S. Interleukin-4 and dexamethasone counterregulate extracellular matrix remodelling and phagocytosis in type-2 macrophages. Scand J Immunol 2005;61(1):10–7. DOI: 10.1111/j.0300-9475.2005.01524.x. PMID: 15644118.</mixed-citation></citation-alternatives></ref><ref id="B16"><label>16.</label><citation-alternatives><mixed-citation xml:lang="en">16. Gratchev A., Guillot P., Hakiy N. et al. Alternatively activated macrophages differentially express fibronectin and its splice variants and the extracellular matrix protein betaIG-H3. Scand J Immunol 2001;53(4):386–92. PMID: 11285119.</mixed-citation><mixed-citation xml:lang="ru">Gratchev A., Guillot P., Hakiy N. et al. Alternatively activated macrophages differentially express fibronectin and its splice variants and the extracellular matrix protein betaIG-H3. Scand J Immunol 2001;53(4):386–92. PMID: 11285119.</mixed-citation></citation-alternatives></ref><ref id="B17"><label>17.</label><citation-alternatives><mixed-citation xml:lang="en">17. Gordon S. Alternative activation of macrophages. Nat Rev Immunol 2003;3(1):23–35. DOI: 10.1038/nri978. PMID: 12511873.</mixed-citation><mixed-citation xml:lang="ru">Gordon S. Alternative activation of macrophages. Nat Rev Immunol 2003;3(1):23–35. DOI: 10.1038/nri978. PMID: 12511873.</mixed-citation></citation-alternatives></ref><ref id="B18"><label>18.</label><citation-alternatives><mixed-citation xml:lang="en">18. Gratchev A., Kzhyshkowska J., Kannookadan S., et al. Activation of a TGF-betaspecific multistep gene expression program in mature macrophages requires glucocorticoid-mediated surface expression of TGF-beta receptor II. J Immunol. 2008;180(10):6553–65.</mixed-citation><mixed-citation xml:lang="ru">Gratchev A., Kzhyshkowska J., Kannookadan S., et al. Activation of a TGF-betaspecific multistep gene expression program in mature macrophages requires glucocorticoid-mediated surface expression of TGF-beta receptor II. J Immunol. 2008;180(10):6553–65.</mixed-citation></citation-alternatives></ref><ref id="B19"><label>19.</label><citation-alternatives><mixed-citation xml:lang="en">19. Gratchev A. TGF-beta signalling in tumour associated macrophages. Immunobiology 2017;222(1):75–81. DOI: 10.1016/j.imbio.2015.11.016.</mixed-citation><mixed-citation xml:lang="ru">Gratchev A. TGF-beta signalling in tumour associated macrophages. Immunobiology 2017;222(1):75–81. DOI: 10.1016/j.imbio.2015.11.016.</mixed-citation></citation-alternatives></ref><ref id="B20"><label>20.</label><citation-alternatives><mixed-citation xml:lang="en">20. Anderson C.F., Gerber J.S., Mosser D.M. Modulating macrophage function with IgG immune complexes. J Endotoxin Res.2002;8(6):477–81. DOI: 10.1179/096805102125001118. PMID: 12697094.</mixed-citation><mixed-citation xml:lang="ru">Anderson C.F., Gerber J.S., Mosser D.M. Modulating macrophage function with IgG immune complexes. J Endotoxin Res.2002;8(6):477–81. DOI: 10.1179/096805102125001118. PMID: 12697094.</mixed-citation></citation-alternatives></ref><ref id="B21"><label>21.</label><citation-alternatives><mixed-citation xml:lang="en">21. Herrero C., Hu X., Li W.P. et al. Reprogramming of IL-10 activity and signaling by INF-γ. J Immunol 2003;171(10): 5034–41. PMID: 14607900.</mixed-citation><mixed-citation xml:lang="ru">Herrero C., Hu X., Li W.P. et al. Reprogramming of IL-10 activity and signaling by INF-γ. J Immunol 2003;171(10): 5034–41. PMID: 14607900.</mixed-citation></citation-alternatives></ref><ref id="B22"><label>22.</label><citation-alternatives><mixed-citation xml:lang="en">22. Kim J., Hematti P. Mesenchymal stem cell-educated macrophages: a novel type of alternatively activated macrophages. Exp Hematol 2009;37(12):1445–53. DOI: 10.1016/j.exphem.2009.09.004. PMID: 19772890.</mixed-citation><mixed-citation xml:lang="ru">Kim J., Hematti P. Mesenchymal stem cell-educated macrophages: a novel type of alternatively activated macrophages. Exp Hematol 2009;37(12):1445–53. DOI: 10.1016/j.exphem.2009.09.004. PMID: 19772890.</mixed-citation></citation-alternatives></ref><ref id="B23"><label>23.</label><citation-alternatives><mixed-citation xml:lang="en">23. Chevrier S., Levine J.H., Zanotelli V.R.T. et al. An immune atlas of clear cell renal cell carcinoma. Cell 2017;169(4):736–49. e18. DOI: 10.1016/j.cell.2017.04.016. PMID: 28475899.</mixed-citation><mixed-citation xml:lang="ru">Chevrier S., Levine J.H., Zanotelli V.R.T. et al. An immune atlas of clear cell renal cell carcinoma. Cell 2017;169(4):736–49. e18. DOI: 10.1016/j.cell.2017.04.016. PMID: 28475899.</mixed-citation></citation-alternatives></ref><ref id="B24"><label>24.</label><citation-alternatives><mixed-citation xml:lang="en">24. Blaser M.J., Perez-Perez G.I., Kleanthous H. et al. Infection with Helicobacter pylori strains possessing cagA is associated with an increased risk of developing adenocarcinoma of the stomach. Cancer Res 1995;55(10):2111–5. PMID: 7743510.</mixed-citation><mixed-citation xml:lang="ru">Blaser M.J., Perez-Perez G.I., Kleanthous H. et al. Infection with Helicobacter pylori strains possessing cagA is associated with an increased risk of developing adenocarcinoma of the stomach. Cancer Res 1995;55(10):2111–5. PMID: 7743510.</mixed-citation></citation-alternatives></ref><ref id="B25"><label>25.</label><citation-alternatives><mixed-citation xml:lang="en">25. Kuper H., Adami H.O., Trichopoulos D. Infections as a major preventable cause of human cancer. J Intern Med 2000;248(3):171–83. PMID: 10971784.</mixed-citation><mixed-citation xml:lang="ru">Kuper H., Adami H.O., Trichopoulos D. Infections as a major preventable cause of human cancer. J Intern Med 2000;248(3):171–83. PMID: 10971784.</mixed-citation></citation-alternatives></ref><ref id="B26"><label>26.</label><citation-alternatives><mixed-citation xml:lang="en">26. Scholl S.M., Pallud C., Beuvon F. et al. Anti-colony-stimulating factor-1 antibody staining in primary breast adenocarcinomas correlates with marked inflammatory cell infiltrates and prognosis. J Natl Cancer Inst 1994;86(2):120–6. PMID: 8271294.</mixed-citation><mixed-citation xml:lang="ru">Scholl S.M., Pallud C., Beuvon F. et al. Anti-colony-stimulating factor-1 antibody staining in primary breast adenocarcinomas correlates with marked inflammatory cell infiltrates and prognosis. J Natl Cancer Inst 1994;86(2):120–6. PMID: 8271294.</mixed-citation></citation-alternatives></ref><ref id="B27"><label>27.</label><citation-alternatives><mixed-citation xml:lang="en">27. Shacter E., Weitzman S.A. Chronic inflammation and cancer. Oncology (WillistonPark) 2002;16(2):217–26.</mixed-citation><mixed-citation xml:lang="ru">Shacter E., Weitzman S.A. Chronic inflammation and cancer. Oncology (WillistonPark) 2002;16(2):217–26.</mixed-citation></citation-alternatives></ref><ref id="B28"><label>28.</label><citation-alternatives><mixed-citation xml:lang="en">28. Maeda H., Akaike T. Nitric oxide and oxygen radicals in infection, inflammation, and cancer. Biochemistry (Mosc) 1998;63(7):854–65. PMID: 9721338.</mixed-citation><mixed-citation xml:lang="ru">Maeda H., Akaike T. Nitric oxide and oxygen radicals in infection, inflammation, and cancer. Biochemistry (Mosc) 1998;63(7):854–65. PMID: 9721338.</mixed-citation></citation-alternatives></ref><ref id="B29"><label>29.</label><citation-alternatives><mixed-citation xml:lang="en">29. Yamanishi Y., Boyle D.L., Rosengren S. et al. Regional analysis of p53 mutations in rheumatoid arthritis synovium. Proc Natl Acad Sci USA 2002;99(15):10025– 30. DOI: 10.1073/pnas.152333199. PMID: 12119414.</mixed-citation><mixed-citation xml:lang="ru">Yamanishi Y., Boyle D.L., Rosengren S. et al. Regional analysis of p53 mutations in rheumatoid arthritis synovium. Proc Natl Acad Sci USA 2002;99(15):10025– 30. DOI: 10.1073/pnas.152333199. PMID: 12119414.</mixed-citation></citation-alternatives></ref><ref id="B30"><label>30.</label><citation-alternatives><mixed-citation xml:lang="en">30. Ernst P.B., Gold B.D. The disease spectrum of Helicobacter pylori: the immunopathogenesis of gastroduodenal ulcer and gastric cancer. Annu Rev Microbiol 2000;54:615–40. PMID: 11018139.</mixed-citation><mixed-citation xml:lang="ru">Ernst P.B., Gold B.D. The disease spectrum of Helicobacter pylori: the immunopathogenesis of gastroduodenal ulcer and gastric cancer. Annu Rev Microbiol 2000;54:615–40. PMID: 11018139.</mixed-citation></citation-alternatives></ref><ref id="B31"><label>31.</label><citation-alternatives><mixed-citation xml:lang="en">31. Hudson J.D., Shoaibi M.A., Maestro R. et al. A proinflammatory cytokine inhibits p53 tumor suppressor activity. J Exp Med 1999;190(10):1375–82. PMID: 10562313.</mixed-citation><mixed-citation xml:lang="ru">Hudson J.D., Shoaibi M.A., Maestro R. et al. A proinflammatory cytokine inhibits p53 tumor suppressor activity. J Exp Med 1999;190(10):1375–82. PMID: 10562313.</mixed-citation></citation-alternatives></ref><ref id="B32"><label>32.</label><citation-alternatives><mixed-citation xml:lang="en">32. Brigati C., Noonan D.M., Albini A., Benelli R. Tumors and inflammatory infiltrates: friends or foes? Clin Exp Metastasis 2002;19(3):247–58. PMID: 12067205.</mixed-citation><mixed-citation xml:lang="ru">Brigati C., Noonan D.M., Albini A., Benelli R. Tumors and inflammatory infiltrates: friends or foes? Clin Exp Metastasis 2002;19(3):247–58. PMID: 12067205.</mixed-citation></citation-alternatives></ref><ref id="B33"><label>33.</label><citation-alternatives><mixed-citation xml:lang="en">33. Leek R.D., Harris A.L. Tumor-associated macrophages in breast cancer. J Mammary Gland Biol Neoplasia 2002;7(2):177–89. PMID: 12463738.</mixed-citation><mixed-citation xml:lang="ru">Leek R.D., Harris A.L. Tumor-associated macrophages in breast cancer. J Mammary Gland Biol Neoplasia 2002;7(2):177–89. PMID: 12463738.</mixed-citation></citation-alternatives></ref><ref id="B34"><label>34.</label><citation-alternatives><mixed-citation xml:lang="en">34. Saji H., Koike M., Yamori T. et al. Significant correlation of monocyte chemoattractant protein-1 expression with neovascularization and progression of breast carcinoma. Cancer 2001;92(5):1085–91. PMID: 11571719.</mixed-citation><mixed-citation xml:lang="ru">Saji H., Koike M., Yamori T. et al. Significant correlation of monocyte chemoattractant protein-1 expression with neovascularization and progression of breast carcinoma. Cancer 2001;92(5):1085–91. PMID: 11571719.</mixed-citation></citation-alternatives></ref><ref id="B35"><label>35.</label><citation-alternatives><mixed-citation xml:lang="en">35. Ueno T., Toi M., Saji H. et al. Significance of macrophage chemoattractant protein-1 in macrophage recruitment, angiogenesis, and survival in human breast cancer. Clin Cancer Res 2000;6(8):3282–9. PMID: 10955814.</mixed-citation><mixed-citation xml:lang="ru">Ueno T., Toi M., Saji H. et al. Significance of macrophage chemoattractant protein-1 in macrophage recruitment, angiogenesis, and survival in human breast cancer. Clin Cancer Res 2000;6(8):3282–9. PMID: 10955814.</mixed-citation></citation-alternatives></ref><ref id="B36"><label>36.</label><citation-alternatives><mixed-citation xml:lang="en">36. Kacinski B.M. CSF-1 and its receptor in ovarian, endometrial and breast cancer. Ann Med 1995;27(1):79–85. PMID: 7742005.</mixed-citation><mixed-citation xml:lang="ru">Kacinski B.M. CSF-1 and its receptor in ovarian, endometrial and breast cancer. Ann Med 1995;27(1):79–85. PMID: 7742005.</mixed-citation></citation-alternatives></ref><ref id="B37"><label>37.</label><citation-alternatives><mixed-citation xml:lang="en">37. Kacinski B.M. CSF-1 and its receptor in breast carcinomas and neoplasms of the female reproductive tract. Mol Reprod Dev 1997;46(1):71–4. DOI: 10.1002/(SICI)1098-2795(199701)46:1&lt;71::AIDMRD11&gt;3.0.CO;2-6. PMID: 8981366.</mixed-citation><mixed-citation xml:lang="ru">Kacinski B.M. CSF-1 and its receptor in breast carcinomas and neoplasms of the female reproductive tract. Mol Reprod Dev 1997;46(1):71–4. DOI: 10.1002/(SICI)1098-2795(199701)46:1&lt;71::AIDMRD11&gt;3.0.CO;2-6. PMID: 8981366.</mixed-citation></citation-alternatives></ref><ref id="B38"><label>38.</label><citation-alternatives><mixed-citation xml:lang="en">38. Lin E.Y., Gouon-Evans V., Nguyen A.V. et al. The macrophage growth factor CSF1 in mammary gland development and tumor progression. J Mammary Gland Biol Neoplasia 2002;7(2):147–62. PMID: 12465600.</mixed-citation><mixed-citation xml:lang="ru">Lin E.Y., Gouon-Evans V., Nguyen A.V. et al. The macrophage growth factor CSF1 in mammary gland development and tumor progression. J Mammary Gland Biol Neoplasia 2002;7(2):147–62. PMID: 12465600.</mixed-citation></citation-alternatives></ref><ref id="B39"><label>39.</label><citation-alternatives><mixed-citation xml:lang="en">39. Smith H.O., Anderson P.S., Kuo D.Y. et al. The role of colony-stimulating factor 1 and its receptor in the etiopathogenesis of endometrial adenocarcinoma. Clin Cancer Res 1995;1(3):313–25. PMID: 9815987.</mixed-citation><mixed-citation xml:lang="ru">Smith H.O., Anderson P.S., Kuo D.Y. et al. The role of colony-stimulating factor 1 and its receptor in the etiopathogenesis of endometrial adenocarcinoma. Clin Cancer Res 1995;1(3):313–25. PMID: 9815987.</mixed-citation></citation-alternatives></ref><ref id="B40"><label>40.</label><citation-alternatives><mixed-citation xml:lang="en">40. Lewis J.S., Landers R.J., Underwood J.C. et al. Expression of vascular endothelial growth factor by macrophages is up- regulated in poorly vascularized areas of breast carcinomas. J Pathol 2000;192(2):150–8. DOI: 10.1002/1096-9896(2000)9999:9999&lt;::AIDPATH687&gt;3.0.CO;2-G. PMID: 11004690.</mixed-citation><mixed-citation xml:lang="ru">Lewis J.S., Landers R.J., Underwood J.C. et al. Expression of vascular endothelial growth factor by macrophages is up- regulated in poorly vascularized areas of breast carcinomas. J Pathol 2000;192(2):150–8. DOI: 10.1002/1096-9896(2000)9999:9999&lt;::AIDPATH687&gt;3.0.CO;2-G. PMID: 11004690.</mixed-citation></citation-alternatives></ref><ref id="B41"><label>41.</label><citation-alternatives><mixed-citation xml:lang="en">41. Eubank T.D., Galloway M., Montague C.M. et al. M-CSF induces vascular endothelial growth factor production and angiogenic activity from human monocytes. J Immunol 2003;171(5):2637–43. PMID: 12928417.</mixed-citation><mixed-citation xml:lang="ru">Eubank T.D., Galloway M., Montague C.M. et al. M-CSF induces vascular endothelial growth factor production and angiogenic activity from human monocytes. J Immunol 2003;171(5):2637–43. PMID: 12928417.</mixed-citation></citation-alternatives></ref><ref id="B42"><label>42.</label><citation-alternatives><mixed-citation xml:lang="en">42. Barleon B., Sozzani S., Zhou D. et al. Migration of human monocytes in response to vascular endothelial growth factor (VEGF) is mediated via the VEGF receptor flt-1. Blood 1996;87(8):3336–43. PMID: 8605350.</mixed-citation><mixed-citation xml:lang="ru">Barleon B., Sozzani S., Zhou D. et al. Migration of human monocytes in response to vascular endothelial growth factor (VEGF) is mediated via the VEGF receptor flt-1. Blood 1996;87(8):3336–43. PMID: 8605350.</mixed-citation></citation-alternatives></ref><ref id="B43"><label>43.</label><citation-alternatives><mixed-citation xml:lang="en">43. Leek R.D., Hunt N.C., Landers R.J. et al. Macrophage infiltration is associated with VEGF and EGFR expression in breast cancer. J Pathol 2000;190(4):430–6. DOI: 10.1002/(SICI)10969896(200003)190:4&lt;430::AIDPATH538&gt;3.0.CO;2-6. PMID: 10699991.</mixed-citation><mixed-citation xml:lang="ru">Leek R.D., Hunt N.C., Landers R.J. et al. Macrophage infiltration is associated with VEGF and EGFR expression in breast cancer. J Pathol 2000;190(4):430–6. DOI: 10.1002/(SICI)10969896(200003)190:4&lt;430::AIDPATH538&gt;3.0.CO;2-6. PMID: 10699991.</mixed-citation></citation-alternatives></ref><ref id="B44"><label>44.</label><citation-alternatives><mixed-citation xml:lang="en">44. Boudreau N., Myers C. Breast cancer-induced angiogenesis: multiple mechanisms and the role of the microenvironment. Breast Cancer Res 2003;5(3):140–6. DOI: 10.1186/bcr589. PMID: 12793895.</mixed-citation><mixed-citation xml:lang="ru">Boudreau N., Myers C. Breast cancer-induced angiogenesis: multiple mechanisms and the role of the microenvironment. Breast Cancer Res 2003;5(3):140–6. DOI: 10.1186/bcr589. PMID: 12793895.</mixed-citation></citation-alternatives></ref><ref id="B45"><label>45.</label><citation-alternatives><mixed-citation xml:lang="en">45. Miles D.W., Happerfield L.C., Naylor M.S. et al. Expression of tumour necrosis factor (TNF alpha) and its receptors in benign and malignant breast tissue. Int J Cancer 1994;56(6):777–82. PMID: 8119765.</mixed-citation><mixed-citation xml:lang="ru">Miles D.W., Happerfield L.C., Naylor M.S. et al. Expression of tumour necrosis factor (TNF alpha) and its receptors in benign and malignant breast tissue. Int J Cancer 1994;56(6):777–82. PMID: 8119765.</mixed-citation></citation-alternatives></ref><ref id="B46"><label>46.</label><citation-alternatives><mixed-citation xml:lang="en">46. Jung Y.J., Isaacs J.S., Lee S. et al. IL-1beta-mediated up-regulation of HIF1alpha via an NFkappaB/COX-2 pathway identifies HIF1 as a critical link between inflammation and oncogenesis. FASEB J 2003;17(14):2115–7. DOI: 10.1096/fj.030329fje. PMID: 12958148.</mixed-citation><mixed-citation xml:lang="ru">Jung Y.J., Isaacs J.S., Lee S. et al. IL-1beta-mediated up-regulation of HIF1alpha via an NFkappaB/COX-2 pathway identifies HIF1 as a critical link between inflammation and oncogenesis. FASEB J 2003;17(14):2115–7. DOI: 10.1096/fj.030329fje. PMID: 12958148.</mixed-citation></citation-alternatives></ref><ref id="B47"><label>47.</label><citation-alternatives><mixed-citation xml:lang="en">47. Balkwill F., Mantovani A. Inflammation and cancer: back to Virchow? Lancet 2001;357(9255):539–45. DOI: 10.1016/S0140-6736(00)04046-0. PMID: 11229684.</mixed-citation><mixed-citation xml:lang="ru">Balkwill F., Mantovani A. Inflammation and cancer: back to Virchow? Lancet 2001;357(9255):539–45. DOI: 10.1016/S0140-6736(00)04046-0. PMID: 11229684.</mixed-citation></citation-alternatives></ref><ref id="B48"><label>48.</label><citation-alternatives><mixed-citation xml:lang="en">48. Stacey K.J., Fowles L.F., Colman M.S. et al. Regulation of urokinase-type plasminogen activator gene transcription by macrophage colony-stimulating factor. Mol Cell Biol 1995;15(6):3430–41. PMID: 7760840.</mixed-citation><mixed-citation xml:lang="ru">Stacey K.J., Fowles L.F., Colman M.S. et al. Regulation of urokinase-type plasminogen activator gene transcription by macrophage colony-stimulating factor. Mol Cell Biol 1995;15(6):3430–41. PMID: 7760840.</mixed-citation></citation-alternatives></ref><ref id="B49"><label>49.</label><citation-alternatives><mixed-citation xml:lang="en">49. Hildenbrand R., Jansen C., Wolf G. et al. Transforming growth factor-beta stimulates urokinase expression in tumor-associated macrophages of the breast. Lab Invest 1998;78(1):59–71. PMID: 9461122.</mixed-citation><mixed-citation xml:lang="ru">Hildenbrand R., Jansen C., Wolf G. et al. Transforming growth factor-beta stimulates urokinase expression in tumor-associated macrophages of the breast. Lab Invest 1998;78(1):59–71. PMID: 9461122.</mixed-citation></citation-alternatives></ref><ref id="B50"><label>50.</label><citation-alternatives><mixed-citation xml:lang="en">50. Foekens J.A., Peters H.A., Look M.P. et al. The urokinase system of plasminogen activation and prognosis in 2780 breast cancer patients. Cancer Res 2000;60(3):636–43. PMID: 10676647.</mixed-citation><mixed-citation xml:lang="ru">Foekens J.A., Peters H.A., Look M.P. et al. The urokinase system of plasminogen activation and prognosis in 2780 breast cancer patients. Cancer Res 2000;60(3):636–43. PMID: 10676647.</mixed-citation></citation-alternatives></ref><ref id="B51"><label>51.</label><citation-alternatives><mixed-citation xml:lang="en">51. Hildenbrand R., Dilger I., Horlin A. et al. Urokinase and macrophages in tumour angiogenesis. Br J Cancer 1995;72(4): 818–23.</mixed-citation><mixed-citation xml:lang="ru">Hildenbrand R., Dilger I., Horlin A. et al. Urokinase and macrophages in tumour angiogenesis. Br J Cancer 1995;72(4): 818–23.</mixed-citation></citation-alternatives></ref><ref id="B52"><label>52.</label><citation-alternatives><mixed-citation xml:lang="en">52. Hildenbrand R., Glienke W., Magdolen V. et al. Urokinase receptor localization in breast cancer and benign lesions assessed by in situ hybridization and immunohistochemistry. Histochem Cell Biol 1998;110(1):27–32. PMID: 9681686.</mixed-citation><mixed-citation xml:lang="ru">Hildenbrand R., Glienke W., Magdolen V. et al. Urokinase receptor localization in breast cancer and benign lesions assessed by in situ hybridization and immunohistochemistry. Histochem Cell Biol 1998;110(1):27–32. PMID: 9681686.</mixed-citation></citation-alternatives></ref><ref id="B53"><label>53.</label><citation-alternatives><mixed-citation xml:lang="en">53. Fox S.B., Taylor M., Grondahl-Hansen J. et al. Plasminogen activator inhibitor-1 as a measure of vascular remodelling in breast cancer. J Pathol 2001;195(2):236–43. DOI: 10.1002/path.931. PMID: 11592104.</mixed-citation><mixed-citation xml:lang="ru">Fox S.B., Taylor M., Grondahl-Hansen J. et al. Plasminogen activator inhibitor-1 as a measure of vascular remodelling in breast cancer. J Pathol 2001;195(2):236–43. DOI: 10.1002/path.931. PMID: 11592104.</mixed-citation></citation-alternatives></ref><ref id="B54"><label>54.</label><citation-alternatives><mixed-citation xml:lang="en">54. Hildenbrand R., Wolf G., Bohme B. et al. Urokinase plasminogen activator receptor (CD87) expression of tumor-associated macrophages in ductal carcinoma in situ, breast cancer, and resident macrophages of normal breast tissue. J Leukoc Biol 1999;66(1):40–9. PMID: 10410988.</mixed-citation><mixed-citation xml:lang="ru">Hildenbrand R., Wolf G., Bohme B. et al. Urokinase plasminogen activator receptor (CD87) expression of tumor-associated macrophages in ductal carcinoma in situ, breast cancer, and resident macrophages of normal breast tissue. J Leukoc Biol 1999;66(1):40–9. PMID: 10410988.</mixed-citation></citation-alternatives></ref><ref id="B55"><label>55.</label><citation-alternatives><mixed-citation xml:lang="en">55. Knoop A., Andreasen P.A., Andersen J.A. et al. Prognostic significance of urokinasetype plasminogen activator and plasminogen activator inhibitor-1 in primary breast cancer. Br J Cancer 1998;77(6):932–40. PMID: 9528837.</mixed-citation><mixed-citation xml:lang="ru">Knoop A., Andreasen P.A., Andersen J.A. et al. Prognostic significance of urokinasetype plasminogen activator and plasminogen activator inhibitor-1 in primary breast cancer. Br J Cancer 1998;77(6):932–40. PMID: 9528837.</mixed-citation></citation-alternatives></ref><ref id="B56"><label>56.</label><citation-alternatives><mixed-citation xml:lang="en">56. Ogmundsdottir H.M., Petursdottir I., Gudmundsdottir I. Interactions between the immune system and breast cancer. Acta Oncol 1995;34(5):647–50. PMID: 7546833.</mixed-citation><mixed-citation xml:lang="ru">Ogmundsdottir H.M., Petursdottir I., Gudmundsdottir I. Interactions between the immune system and breast cancer. Acta Oncol 1995;34(5):647–50. PMID: 7546833.</mixed-citation></citation-alternatives></ref><ref id="B57"><label>57.</label><citation-alternatives><mixed-citation xml:lang="en">57. Menard S., Tagliabue E., Campiglio M., Pupa S.M. Role of HER2 gene overexpression in breast carcinoma. J Cell Physiol 2000;182(2):150–62. DOI: 10.1002/(SICI)1097-4652(200002)182:2&lt;150::AIDJCP3&gt;3.0.CO;2-E. PMID: 10623878.</mixed-citation><mixed-citation xml:lang="ru">Menard S., Tagliabue E., Campiglio M., Pupa S.M. Role of HER2 gene overexpression in breast carcinoma. J Cell Physiol 2000;182(2):150–62. DOI: 10.1002/(SICI)1097-4652(200002)182:2&lt;150::AIDJCP3&gt;3.0.CO;2-E. PMID: 10623878.</mixed-citation></citation-alternatives></ref><ref id="B58"><label>58.</label><citation-alternatives><mixed-citation xml:lang="en">58. Nicholson S., Richard J., Sainsbury C. et al. Epidermal growth factor receptor (EGFr); results of a 6 year follow-up study in operable breast cancer with emphasis on the node negative subgroup. Br J Cancer 1991;63(1):146–50. PMID: 1846551.</mixed-citation><mixed-citation xml:lang="ru">Nicholson S., Richard J., Sainsbury C. et al. Epidermal growth factor receptor (EGFr); results of a 6 year follow-up study in operable breast cancer with emphasis on the node negative subgroup. Br J Cancer 1991;63(1):146–50. PMID: 1846551.</mixed-citation></citation-alternatives></ref><ref id="B59"><label>59.</label><citation-alternatives><mixed-citation xml:lang="en">59. O'Sullivan C., Lewis C.E., Harris A.L., McGee J.O. Secretion of epidermal growth factor by macrophages associated with breast carcinoma. Lancet 1993;342(8864):148–9. PMID: 8101258.</mixed-citation><mixed-citation xml:lang="ru">O'Sullivan C., Lewis C.E., Harris A.L., McGee J.O. Secretion of epidermal growth factor by macrophages associated with breast carcinoma. Lancet 1993;342(8864):148–9. PMID: 8101258.</mixed-citation></citation-alternatives></ref><ref id="B60"><label>60.</label><citation-alternatives><mixed-citation xml:lang="en">60. Wyckoff J.B., Segall J.E., Condeelis J.S. The collection of the motile population of cells from a living tumor. Cancer Res 2000;60(19):5401–4. PMID: 11034079.</mixed-citation><mixed-citation xml:lang="ru">Wyckoff J.B., Segall J.E., Condeelis J.S. The collection of the motile population of cells from a living tumor. Cancer Res 2000;60(19):5401–4. PMID: 11034079.</mixed-citation></citation-alternatives></ref><ref id="B61"><label>61.</label><citation-alternatives><mixed-citation xml:lang="en">61. Lin E.Y., Nguyen A.V., Russell R.G., Pollard J.W. Colony-stimulating factor 1 promotes progression of mammary tumors to malignancy. J Exp Med 2001;193(6): 727–40. PMID: 11257139.</mixed-citation><mixed-citation xml:lang="ru">Lin E.Y., Nguyen A.V., Russell R.G., Pollard J.W. Colony-stimulating factor 1 promotes progression of mammary tumors to malignancy. J Exp Med 2001;193(6): 727–40. PMID: 11257139.</mixed-citation></citation-alternatives></ref><ref id="B62"><label>62.</label><citation-alternatives><mixed-citation xml:lang="en">62. Arnott C.H., Scott K.A., Moore R.J. et al. Tumour necrosis factor-alpha mediates tumour promotion via a PKC alpha- and AP-1-dependent pathway. Oncogene 2002;21(31):4728–38. DOI: 10.1038/sj.onc.1205588. PMID: 12101411.</mixed-citation><mixed-citation xml:lang="ru">Arnott C.H., Scott K.A., Moore R.J. et al. Tumour necrosis factor-alpha mediates tumour promotion via a PKC alpha- and AP-1-dependent pathway. Oncogene 2002;21(31):4728–38. DOI: 10.1038/sj.onc.1205588. PMID: 12101411.</mixed-citation></citation-alternatives></ref><ref id="B63"><label>63.</label><citation-alternatives><mixed-citation xml:lang="en">63. Fischer C., Jonckx B., Mazzone M. et al. Anti-PlGF inhibits growth of VEGF(R)inhibitor-resistant tumors without affecting healthy vessels. Cell 2007;131(3): 463–75. DOI: 10.1016/j.cell.2007.08.038. PMID: 17981115.</mixed-citation><mixed-citation xml:lang="ru">Fischer C., Jonckx B., Mazzone M. et al. Anti-PlGF inhibits growth of VEGF(R)inhibitor-resistant tumors without affecting healthy vessels. Cell 2007;131(3): 463–75. DOI: 10.1016/j.cell.2007.08.038. PMID: 17981115.</mixed-citation></citation-alternatives></ref><ref id="B64"><label>64.</label><citation-alternatives><mixed-citation xml:lang="en">64. Zhang W., Zhu X.D., Sun H.C. et al. Depletion of tumor-associated macrophages enhances the effect of sorafenib in metastatic liver cancer models by antimetastatic and antiangiogenic effects. Clin Cancer Res 2010;16(13):3420–30. DOI: 10.1158/10780432.CCR-09-2904. PMID: 20570927.</mixed-citation><mixed-citation xml:lang="ru">Zhang W., Zhu X.D., Sun H.C. et al. Depletion of tumor-associated macrophages enhances the effect of sorafenib in metastatic liver cancer models by antimetastatic and antiangiogenic effects. Clin Cancer Res 2010;16(13):3420–30. DOI: 10.1158/10780432.CCR-09-2904. PMID: 20570927.</mixed-citation></citation-alternatives></ref><ref id="B65"><label>65.</label><citation-alternatives><mixed-citation xml:lang="en">65. Wang F., Yang L., Gao Q. et al. CD163+CD14+ macrophages, a potential immune biomarker for malignant pleural effusion. Cancer Immunol Immunother 2015;64(8):965–76. DOI: 10.1007/s00262-015-1701-9. PMID: 25944005.</mixed-citation><mixed-citation xml:lang="ru">Wang F., Yang L., Gao Q. et al. CD163+CD14+ macrophages, a potential immune biomarker for malignant pleural effusion. Cancer Immunol Immunother 2015;64(8):965–76. DOI: 10.1007/s00262-015-1701-9. PMID: 25944005.</mixed-citation></citation-alternatives></ref><ref id="B66"><label>66.</label><citation-alternatives><mixed-citation xml:lang="en">66. Andersen M.N., Abildgaard N., Maniec- ki M.B. et al. Monocyte/macrophage-de rived soluble CD163: a novel biomarker in multiple myeloma. Eur J Haemato. 2014;93(1):41–7. DOI: 10.1111/ejh.12296. PMID: 24612259.</mixed-citation><mixed-citation xml:lang="ru">Andersen M.N., Abildgaard N., Maniec- ki M.B. et al. Monocyte/macrophage-de rived soluble CD163: a novel biomarker in multiple myeloma. Eur J Haemato. 2014;93(1):41–7. DOI: 10.1111/ejh.12296. PMID: 24612259.</mixed-citation></citation-alternatives></ref><ref id="B67"><label>67.</label><citation-alternatives><mixed-citation xml:lang="en">67. Tang X. Tumor-associated macrophages as potential diagnostic and prognostic biomarkers in breast cancer. Cancer Lett 2013;332(1):3–10. DOI: 10.1016/j.canlet.2013.01.024. PMID: 23348699.</mixed-citation><mixed-citation xml:lang="ru">Tang X. Tumor-associated macrophages as potential diagnostic and prognostic biomarkers in breast cancer. Cancer Lett 2013;332(1):3–10. DOI: 10.1016/j.canlet.2013.01.024. PMID: 23348699.</mixed-citation></citation-alternatives></ref><ref id="B68"><label>68.</label><citation-alternatives><mixed-citation xml:lang="en">68. Adams D.L., Martin S.S., Alpaugh R.K. et al. Circulating giant macrophages as a potential biomarker of solid tumors. Proc Natl Acad Sci USA 2014;111(9):3514–9. DOI: 10.1073/pnas.1320198111. PMID: 24550495.</mixed-citation><mixed-citation xml:lang="ru">Adams D.L., Martin S.S., Alpaugh R.K. et al. Circulating giant macrophages as a potential biomarker of solid tumors. Proc Natl Acad Sci USA 2014;111(9):3514–9. DOI: 10.1073/pnas.1320198111. PMID: 24550495.</mixed-citation></citation-alternatives></ref><ref id="B69"><label>69.</label><citation-alternatives><mixed-citation xml:lang="en">69. Forssell J., Oberg A., Henriksson M.L. et al. High macrophage infiltration along the tumor front correlates with improved survival in colon cancer. Clin Cancer Res 2007;13(5):1472–9. DOI: 10.1158/10780432.CCR-06-2073. PMID: 17332291.</mixed-citation><mixed-citation xml:lang="ru">Forssell J., Oberg A., Henriksson M.L. et al. High macrophage infiltration along the tumor front correlates with improved survival in colon cancer. Clin Cancer Res 2007;13(5):1472–9. DOI: 10.1158/10780432.CCR-06-2073. PMID: 17332291.</mixed-citation></citation-alternatives></ref><ref id="B70"><label>70.</label><citation-alternatives><mixed-citation xml:lang="en">70. Wang B., Xu D., Yu X. et al. Association of intra-tumoral infiltrating macrophages and regulatory T cells is an independent prognostic factor in gastric cancer after radical resection. Ann Surg Oncol 2011;18(9):2585–93. DOI: 10.1245/s10434-011-1609-3. PMID: 21347781.</mixed-citation><mixed-citation xml:lang="ru">Wang B., Xu D., Yu X. et al. Association of intra-tumoral infiltrating macrophages and regulatory T cells is an independent prognostic factor in gastric cancer after radical resection. Ann Surg Oncol 2011;18(9):2585–93. DOI: 10.1245/s10434-011-1609-3. PMID: 21347781.</mixed-citation></citation-alternatives></ref><ref id="B71"><label>71.</label><citation-alternatives><mixed-citation xml:lang="en">71. Shimura S., Yang G., Ebara S. et al. Reduced infiltration of tumor-associated macrophages in human prostate cancer: association with cancer progression. Cancer Res 2000;60(20):5857–61. PMID: 11059783.</mixed-citation><mixed-citation xml:lang="ru">Shimura S., Yang G., Ebara S. et al. Reduced infiltration of tumor-associated macrophages in human prostate cancer: association with cancer progression. Cancer Res 2000;60(20):5857–61. PMID: 11059783.</mixed-citation></citation-alternatives></ref><ref id="B72"><label>72.</label><citation-alternatives><mixed-citation xml:lang="en">72. Robinson S.C., Scott K.A., Wilson J.L. et al. A chemokine receptor antagonist inhibits experimental breast tumor growth. Cancer Res 2003;63(23):8360–5. PMID: 14678997.</mixed-citation><mixed-citation xml:lang="ru">Robinson S.C., Scott K.A., Wilson J.L. et al. A chemokine receptor antagonist inhibits experimental breast tumor growth. Cancer Res 2003;63(23):8360–5. PMID: 14678997.</mixed-citation></citation-alternatives></ref><ref id="B73"><label>73.</label><citation-alternatives><mixed-citation xml:lang="en">73. Coscia M., Quaglino E., Iezzi M. et al. Zoledronic acid repolarizes tumour-associated macrophages and inhibits mammary carcinogenesis by targeting the mevalonate pathway. J Cell Mol Med 2010;14(12):2803–15. DOI: 10.1111/j.1582-4934.2009.00926.x. PMID: 19818098.</mixed-citation><mixed-citation xml:lang="ru">Coscia M., Quaglino E., Iezzi M. et al. Zoledronic acid repolarizes tumour-associated macrophages and inhibits mammary carcinogenesis by targeting the mevalonate pathway. J Cell Mol Med 2010;14(12):2803–15. DOI: 10.1111/j.1582-4934.2009.00926.x. PMID: 19818098.</mixed-citation></citation-alternatives></ref><ref id="B74"><label>74.</label><citation-alternatives><mixed-citation xml:lang="en">74. Hamilton J.A., Achuthan A. Colony stimulating factors and myeloid cell biology in health and disease. Trends Immunol 2013;34(2):81–9. DOI: 10.1016/j.it.2012.08.006. PMID: 23000011.</mixed-citation><mixed-citation xml:lang="ru">Hamilton J.A., Achuthan A. Colony stimulating factors and myeloid cell biology in health and disease. Trends Immunol 2013;34(2):81–9. DOI: 10.1016/j.it.2012.08.006. PMID: 23000011.</mixed-citation></citation-alternatives></ref><ref id="B75"><label>75.</label><citation-alternatives><mixed-citation xml:lang="en">75. Komohara Y., Jinushi M., Takeya M. Clinical significance of macrophage heterogeneity in human malignant tumors. Cancer Sci 2014;105(1):1–8. DOI: 10.1111/cas.12314. PMID: 24168081.</mixed-citation><mixed-citation xml:lang="ru">Komohara Y., Jinushi M., Takeya M. Clinical significance of macrophage heterogeneity in human malignant tumors. Cancer Sci 2014;105(1):1–8. DOI: 10.1111/cas.12314. PMID: 24168081.</mixed-citation></citation-alternatives></ref><ref id="B76"><label>76.</label><citation-alternatives><mixed-citation xml:lang="en">76. Sica A., Mantovani A. Macrophage plasticity and polarization: in vivo veritas. J Clin Invest 2012;122(3):787–95. DOI: 10.1172/JCI59643. PMID: 22378047.</mixed-citation><mixed-citation xml:lang="ru">Sica A., Mantovani A. Macrophage plasticity and polarization: in vivo veritas. J Clin Invest 2012;122(3):787–95. DOI: 10.1172/JCI59643. PMID: 22378047.</mixed-citation></citation-alternatives></ref><ref id="B77"><label>77.</label><citation-alternatives><mixed-citation xml:lang="en">77. Pello O.M., De Pizzol M., Mirolo M. et al. Role of c-Myc in alternative activation of human macrophages and tumorassociated macrophage biology. Blood 2012;119(2):411–21. DOI: 10.1182/blood-2011-02-339911. PMID: 22067385.</mixed-citation><mixed-citation xml:lang="ru">Pello O.M., De Pizzol M., Mirolo M. et al. Role of c-Myc in alternative activation of human macrophages and tumorassociated macrophage biology. Blood 2012;119(2):411–21. DOI: 10.1182/blood-2011-02-339911. PMID: 22067385.</mixed-citation></citation-alternatives></ref><ref id="B78"><label>78.</label><citation-alternatives><mixed-citation xml:lang="en">78. Satoh T., Takeuchi O., Vandenbon A. et al. The Jmjd3-Irf4 axis regulates M2 macrophage polarization and host responses against helminth infection. Nature Immunol 2010;11(10):936–44. DOI: 10.1038/ni.1920.</mixed-citation><mixed-citation xml:lang="ru">Satoh T., Takeuchi O., Vandenbon A. et al. The Jmjd3-Irf4 axis regulates M2 macrophage polarization and host responses against helminth infection. Nature Immunol 2010;11(10):936–44. DOI: 10.1038/ni.1920.</mixed-citation></citation-alternatives></ref><ref id="B79"><label>79.</label><citation-alternatives><mixed-citation xml:lang="en">79. Lawrence T., Natoli G. Transcriptional regulation of macrophage polarization: enabling diversity with identity. Nat Rev Immunol 2011;11(11):750–61. DOI: 10.1038/nri3088. PMID: 22025054.</mixed-citation><mixed-citation xml:lang="ru">Lawrence T., Natoli G. Transcriptional regulation of macrophage polarization: enabling diversity with identity. Nat Rev Immunol 2011;11(11):750–61. DOI: 10.1038/nri3088. PMID: 22025054.</mixed-citation></citation-alternatives></ref><ref id="B80"><label>80.</label><citation-alternatives><mixed-citation xml:lang="en">80. Germano G., Frapolli R., Belgiovine C. et al. Role of macrophage targeting in the antitumor activity of trabectedin. Cancer Cell 2013;23(2):249–62. DOI: 10.1016/j.ccr.2013.01.008. PMID: 23410977.</mixed-citation><mixed-citation xml:lang="ru">Germano G., Frapolli R., Belgiovine C. et al. Role of macrophage targeting in the antitumor activity of trabectedin. Cancer Cell 2013;23(2):249–62. DOI: 10.1016/j.ccr.2013.01.008. PMID: 23410977.</mixed-citation></citation-alternatives></ref><ref id="B81"><label>81.</label><citation-alternatives><mixed-citation xml:lang="en">81. Gabrusiewicz K., Ellert-Miklaszewska A., Lipko M. et al. Characteristics of the alternative phenotype of microglia/macrophages and its modulation in experimental gliomas. PLoS One 2011;6(8):e23902. DOI: 10.1371/journal.pone.0023902. PMID: 21901144.</mixed-citation><mixed-citation xml:lang="ru">Gabrusiewicz K., Ellert-Miklaszewska A., Lipko M. et al. Characteristics of the alternative phenotype of microglia/macrophages and its modulation in experimental gliomas. PLoS One 2011;6(8):e23902. DOI: 10.1371/journal.pone.0023902. PMID: 21901144.</mixed-citation></citation-alternatives></ref><ref id="B82"><label>82.</label><citation-alternatives><mixed-citation xml:lang="en">82. Rogers T.L., Holen I. Tumour macrophages as potential targets of bisphosphonates. J Transl Med 2011;9:177. DOI: 10.1186/14795876-9-177. PMID: 22005011.</mixed-citation><mixed-citation xml:lang="ru">Rogers T.L., Holen I. Tumour macrophages as potential targets of bisphosphonates. J Transl Med 2011;9:177. DOI: 10.1186/14795876-9-177. PMID: 22005011.</mixed-citation></citation-alternatives></ref><ref id="B83"><label>83.</label><citation-alternatives><mixed-citation xml:lang="en">83. van Ginderachter J.A., Movahedi K., Van den Bossche J. et al. Macrophages, PPARs, and Cancer. PPAR Res 2008;2008:169414. DOI: 10.1155/2008/169414.</mixed-citation><mixed-citation xml:lang="ru">van Ginderachter J.A., Movahedi K., Van den Bossche J. et al. Macrophages, PPARs, and Cancer. PPAR Res 2008;2008:169414. DOI: 10.1155/2008/169414.</mixed-citation></citation-alternatives></ref><ref id="B84"><label>84.</label><citation-alternatives><mixed-citation xml:lang="en">84. Lewis C., Murdoch C. Macrophage responses to hypoxia: implications for tumor progression and anti-cancer therapies. Am J Pathol 2005;167(3):627–35. DOI: 10.1016/S0002-9440(10)62038-X. PMID: 16127144.</mixed-citation><mixed-citation xml:lang="ru">Lewis C., Murdoch C. Macrophage responses to hypoxia: implications for tumor progression and anti-cancer therapies. Am J Pathol 2005;167(3):627–35. DOI: 10.1016/S0002-9440(10)62038-X. PMID: 16127144.</mixed-citation></citation-alternatives></ref><ref id="B85"><label>85.</label><citation-alternatives><mixed-citation xml:lang="en">85. Doedens A.L., Stockmann C., Rubin- stein M.P. et al. Macrophage expression of hypoxia-inducible factor-1 alpha suppresses T-cell function and promotes tumor progression. Cancer Res 2010;70(19):7465–75. DOI: 10.1158/0008-5472.CAN-10-1439. PMID: 20841473.</mixed-citation><mixed-citation xml:lang="ru">Doedens A.L., Stockmann C., Rubin- stein M.P. et al. Macrophage expression of hypoxia-inducible factor-1 alpha suppresses T-cell function and promotes tumor progression. Cancer Res 2010;70(19):7465–75. DOI: 10.1158/0008-5472.CAN-10-1439. PMID: 20841473.</mixed-citation></citation-alternatives></ref><ref id="B86"><label>86.</label><citation-alternatives><mixed-citation xml:lang="en">86. Watkins S.K., Egilmez N.K., Suttles J. et al. IL-12 rapidly alters the functional profile of tumor-associated and tumor-infiltrating macrophages in vitro and in vivo. J Immunol 2007;178(3):1357–62. PMID: 17237382.</mixed-citation><mixed-citation xml:lang="ru">Watkins S.K., Egilmez N.K., Suttles J. et al. IL-12 rapidly alters the functional profile of tumor-associated and tumor-infiltrating macrophages in vitro and in vivo. J Immunol 2007;178(3):1357–62. PMID: 17237382.</mixed-citation></citation-alternatives></ref><ref id="B87"><label>87.</label><citation-alternatives><mixed-citation xml:lang="en">87. Qian B.Z., Li J., Zhang H. et al. CCL2 recruits inflammatory monocytes to facilitate breast-tumour metastasis. Nature 2011;475(7355):222–5. DOI:10.1038/nature10138. PMID: 21654748.</mixed-citation><mixed-citation xml:lang="ru">Qian B.Z., Li J., Zhang H. et al. CCL2 recruits inflammatory monocytes to facilitate breast-tumour metastasis. Nature 2011;475(7355):222–5. DOI:10.1038/nature10138. PMID: 21654748.</mixed-citation></citation-alternatives></ref><ref id="B88"><label>88.</label><citation-alternatives><mixed-citation xml:lang="en">88. Roland C.L., Dineen S.P., Lynn K.D. et al. Inhibition of vascular endothelial growth factor reduces angiogenesis and modulates immune cell infiltration of orthotopic breast cancer xenografts. Mol Cancer Ther 2009;8(7):1761–71. DOI: 10.1158/1535-7163.MCT-09-0280. PMID: 19567820.</mixed-citation><mixed-citation xml:lang="ru">Roland C.L., Dineen S.P., Lynn K.D. et al. Inhibition of vascular endothelial growth factor reduces angiogenesis and modulates immune cell infiltration of orthotopic breast cancer xenografts. Mol Cancer Ther 2009;8(7):1761–71. DOI: 10.1158/1535-7163.MCT-09-0280. PMID: 19567820.</mixed-citation></citation-alternatives></ref></ref-list></back></article>
