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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">Tumors of female reproductive system</journal-id><journal-title-group><journal-title xml:lang="en">Tumors of female reproductive system</journal-title><trans-title-group xml:lang="ru"><trans-title>Опухоли женской репродуктивной системы</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1994-4098</issn><issn publication-format="electronic">1999-8627</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">50</article-id><article-id pub-id-type="doi">10.17650/1994-4098-2013-0-3-4-12-17</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>MAMMOLOGY. TOPICAL ISSUE</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>МАММОЛОГИЯ. АКТУАЛЬНАЯ ТЕМА</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">Role of a cyclooxygenase-2 cascade in breast cancer cell dissemination</article-title><trans-title-group xml:lang="ru"><trans-title>Роль каскада циклооксигеназы-2 в метастазировании рака молочной железы</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Taipov</surname><given-names>M. A.</given-names></name><name xml:lang="ru"><surname>Таипов</surname><given-names>М. А.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>taipoff.m@yandex.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Kudryavtsev</surname><given-names>I. A.</given-names></name><name xml:lang="ru"><surname>Кудрявцев</surname><given-names>И. А.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Laktionov</surname><given-names>K. P.</given-names></name><name xml:lang="ru"><surname>Лактионов</surname><given-names>К. П.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Levchenko</surname><given-names>N. E.</given-names></name><name xml:lang="ru"><surname>Левченко</surname><given-names>Н. Е.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Shevchenko</surname><given-names>V. E.</given-names></name><name xml:lang="ru"><surname>Шевченко</surname><given-names>В. Е.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">N.N. Blokhin Russian Cancer Research Center, Russian Academy of Medical Sciences, Moscow</institution></aff><aff><institution xml:lang="ru">ФГБУ «РОНЦ им. Н.Н. Блохина» РАМН, Москва</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2013-09-22" publication-format="electronic"><day>22</day><month>09</month><year>2013</year></pub-date><issue>3-4</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>12</fpage><lpage>17</lpage><history><date date-type="received" iso-8601-date="2014-07-22"><day>22</day><month>07</month><year>2014</year></date><date date-type="accepted" iso-8601-date="2014-07-22"><day>22</day><month>07</month><year>2014</year></date></history><permissions><copyright-year>2013</copyright-year><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/></permissions><self-uri xlink:href="https://ojrs.abvpress.ru/ojrs/article/view/50">https://ojrs.abvpress.ru/ojrs/article/view/50</self-uri><abstract xml:lang="en"><p>Current therapeutic approaches based on a study of the genetic portrait of a tumor individualize treatment policy to a greater extent, which cre- ates real prospects for the increasing number of patients to recover. Experimental and clinical evidence suggest that the increased expression of the COX-2 gene increases the risk for breast cancer (BC) cell dissemination into distant organs. A number of recent studies have revealed that selec- tive COX-2 inhibitors are able to suppress proliferation, to induce apoptosis in the BC cells, and to inhibit tumor neoangiogenesis. However, this area contains many unclear and disputable problems to be still experimentally solved. Our review deals with the theoretical prerequisites for and the analysis of a role of COX-2 in BC cell dissemination.</p></abstract><trans-abstract xml:lang="ru"><p>Современные подходы в терапии, основанные на изучении генетического портрета опухоли, все сильнее индивидуализируют ле- чебную тактику, что создает реальные перспективы выздоровления все большего числа пациенток. Экспериментальные и кли- нические данные показали, что повышенная экспрессия гена СОХ-2 увеличивает риск метастазирования рака молочной железы (РМЖ) в отдаленные органы. В ряде исследований последних лет обнаружено, что селективные ингибиторы фермента СОХ-2 способны тормозить пролиферацию, индуцировать апоптоз клеток РМЖ и угнетать неоангиогенез в опухоли. Однако в этой области много неясных и спорных вопросов, экспериментальное решение которых еще впереди. Наш обзор посвящен теоретическим предпосылкам и анализу результатов исследований роли COX-2 в метастазировании РМЖ.</p></trans-abstract><kwd-group xml:lang="en"><kwd>breast cancer</kwd><kwd>COX-2</kwd><kwd>COX-1</kwd><kwd>prostaglandins</kwd><kwd>PGE2</kwd><kwd>signaling pathway</kwd><kwd>markers for tumor dissemination</kwd><kwd>targets for goal- oriented therapy</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>рак молочной железы</kwd><kwd>СOX-2</kwd><kwd>СOX-1</kwd><kwd>простагландины</kwd><kwd>PGE2</kwd><kwd>сигнальный путь</kwd><kwd>маркеры метастазирования</kwd><kwd>мишени для таргетной терапии</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><citation-alternatives><mixed-citation xml:lang="en">1. Matsuda T., Saika K. Worldwide burden of cancer incidence in 2002 extrapolated from cancer incidence in five continents Vol. IX. Jpn J Clin Oncol 2012;42(11):1111–2.</mixed-citation><mixed-citation xml:lang="ru">Matsuda T., Saika K. Worldwide burden of cancer incidence in 2002 extrapolated from cancer incidence in five continents Vol. IX. Jpn J Clin Oncol 2012;42(11):1111–2.</mixed-citation></citation-alternatives></ref><ref id="B2"><label>2.</label><citation-alternatives><mixed-citation xml:lang="en">2. Bray F., McCarron P., Parkin D.M. The changing global patterns of female breast cancer incidence and mortality. Breast Cancer Res 2004;6(6):229–39.</mixed-citation><mixed-citation xml:lang="ru">Bray F., McCarron P., Parkin D.M. The changing global patterns of female breast cancer incidence and mortality. Breast Cancer Res 2004;6(6):229–39.</mixed-citation></citation-alternatives></ref><ref id="B3"><label>3.</label><citation-alternatives><mixed-citation xml:lang="en">3. Yako-Suketomo H., Saika K .Worldwide burden of cancer incidence below the age of 40 in 2002 extrapolated from the Cancer Incidence in Five Continents Vol. IX. Jpn J Clin Oncol 2013;43(3):343–4.</mixed-citation><mixed-citation xml:lang="ru">Yako-Suketomo H., Saika K .Worldwide burden of cancer incidence below the age of 40 in 2002 extrapolated from the Cancer Incidence in Five Continents Vol. IX. Jpn J Clin Oncol 2013;43(3):343–4.</mixed-citation></citation-alternatives></ref><ref id="B4"><label>4.</label><citation-alternatives><mixed-citation xml:lang="en">4. Статистика злокачественных новообразований в России и странах СНГ в 2009 году. Под ред. М.И. Давыдова, Е.М. Аксель. Вестн РОНЦ 2011;22(3 Прил 1):3–170.</mixed-citation><mixed-citation xml:lang="ru">Статистика злокачественных новообразований в России и странах СНГ в 2009 году. Под ред. М.И. Давыдова, Е.М. Аксель. Вестн РОНЦ 2011;22(3 Прил 1):3–170.</mixed-citation></citation-alternatives></ref><ref id="B5"><label>5.</label><citation-alternatives><mixed-citation xml:lang="en">5. Comen E., Norton L., Massague J. Breast cancer tumor size, nodal status, and prognosis: biology trumps anatomy. J Clin Oncol 2011;29(19):2610–2.</mixed-citation><mixed-citation xml:lang="ru">Comen E., Norton L., Massague J. Breast cancer tumor size, nodal status, and prognosis: biology trumps anatomy. J Clin Oncol 2011;29(19):2610–2.</mixed-citation></citation-alternatives></ref><ref id="B6"><label>6.</label><citation-alternatives><mixed-citation xml:lang="en">6. Wiwanitkit V. Combination of EGFR and COX-2 inhibitors in breast cancer patient. Tumour Biol 2012;33(4):1261.</mixed-citation><mixed-citation xml:lang="ru">Wiwanitkit V. Combination of EGFR and COX-2 inhibitors in breast cancer patient. Tumour Biol 2012;33(4):1261.</mixed-citation></citation-alternatives></ref><ref id="B7"><label>7.</label><citation-alternatives><mixed-citation xml:lang="en">7. Petersen M., Pardali E., van der Horst G. et al. Smad2 and Smad3 have opposing roles in breast cancer bone metastasis by differentially affecting tumor angiogenesis. Oncogene 2010;29(9):1351–61.</mixed-citation><mixed-citation xml:lang="ru">Petersen M., Pardali E., van der Horst G. et al. Smad2 and Smad3 have opposing roles in breast cancer bone metastasis by differentially affecting tumor angiogenesis. Oncogene 2010;29(9):1351–61.</mixed-citation></citation-alternatives></ref><ref id="B8"><label>8.</label><citation-alternatives><mixed-citation xml:lang="en">8. Basolo F., Fiore L., Ciardiello F. et al. Response of normal and oncogene- transformed human mammary epithelial cells to transforming growth factor beta 1 (TGF- beta 1): lack of growth-inhibitory effect on cells expressing the simian virus 40 large-T antigen. Int J Cancer 1994;56(5):736–42.</mixed-citation><mixed-citation xml:lang="ru">Basolo F., Fiore L., Ciardiello F. et al. Response of normal and oncogene- transformed human mammary epithelial cells to transforming growth factor beta 1 (TGF- beta 1): lack of growth-inhibitory effect on cells expressing the simian virus 40 large-T antigen. Int J Cancer 1994;56(5):736–42.</mixed-citation></citation-alternatives></ref><ref id="B9"><label>9.</label><citation-alternatives><mixed-citation xml:lang="en">9. Ashok V., Dash C., Rohan T.E. et al. Selective cyclooxygenase-2 (COX-2) inhibitors and breast cancer risk. Breast 2011;20(1):66–70.</mixed-citation><mixed-citation xml:lang="ru">Ashok V., Dash C., Rohan T.E. et al. Selective cyclooxygenase-2 (COX-2) inhibitors and breast cancer risk. Breast 2011;20(1):66–70.</mixed-citation></citation-alternatives></ref><ref id="B10"><label>10.</label><citation-alternatives><mixed-citation xml:lang="en">10. Fu J.Y., Masferrer J.L., Seibert K. et al. The induction and suppression of prostaglandin H2 synthase (cyclooxygenase) in human monocytes. J Biol Chem 1990;265(28):16737–40.</mixed-citation><mixed-citation xml:lang="ru">Fu J.Y., Masferrer J.L., Seibert K. et al. The induction and suppression of prostaglandin H2 synthase (cyclooxygenase) in human monocytes. J Biol Chem 1990;265(28):16737–40.</mixed-citation></citation-alternatives></ref><ref id="B11"><label>11.</label><citation-alternatives><mixed-citation xml:lang="en">11. Xie W.L., Chipman J.G., Robertson D.L. et al. Expression of a mitogen-responsive gene encoding prostaglandin synthase is regulated by mRNA splicing. Proc Natl Acad Sci USA 1991;88(7):2692–6.</mixed-citation><mixed-citation xml:lang="ru">Xie W.L., Chipman J.G., Robertson D.L. et al. Expression of a mitogen-responsive gene encoding prostaglandin synthase is regulated by mRNA splicing. Proc Natl Acad Sci USA 1991;88(7):2692–6.</mixed-citation></citation-alternatives></ref><ref id="B12"><label>12.</label><citation-alternatives><mixed-citation xml:lang="en">12. Kraemer S.A., Meade E.A., DeWitt D.L. Prostaglandin endoperoxide synthase gene structure: identification of the transcriptional start site and 5'-flanking regulatory sequences. Arch Biochem Biophys 1992;293(2):391–400.</mixed-citation><mixed-citation xml:lang="ru">Kraemer S.A., Meade E.A., DeWitt D.L. Prostaglandin endoperoxide synthase gene structure: identification of the transcriptional start site and 5'-flanking regulatory sequences. Arch Biochem Biophys 1992;293(2):391–400.</mixed-citation></citation-alternatives></ref><ref id="B13"><label>13.</label><citation-alternatives><mixed-citation xml:lang="en">13. Garavito R.M., DeWitt D.L. The cyclooxygenase isoforms: structural insights into the conversion of arachidonic acid to prostaglandins. Biochim Biophys Acta 1999;1441(2–3):278–87.</mixed-citation><mixed-citation xml:lang="ru">Garavito R.M., DeWitt D.L. The cyclooxygenase isoforms: structural insights into the conversion of arachidonic acid to prostaglandins. Biochim Biophys Acta 1999;1441(2–3):278–87.</mixed-citation></citation-alternatives></ref><ref id="B14"><label>14.</label><citation-alternatives><mixed-citation xml:lang="en">14. Jana D., Sarkar D.K., Maji A. et al. Can cyclo-oxygenase-2 be a useful prognostic and risk stratification marker in breast cancer? J Indian Med Assoc 2012;110(7):429–33.</mixed-citation><mixed-citation xml:lang="ru">Jana D., Sarkar D.K., Maji A. et al. Can cyclo-oxygenase-2 be a useful prognostic and risk stratification marker in breast cancer? J Indian Med Assoc 2012;110(7):429–33.</mixed-citation></citation-alternatives></ref><ref id="B15"><label>15.</label><citation-alternatives><mixed-citation xml:lang="en">15. Vane J.R., Bakhle Y.S., Botting R.M. Cyclooxygenases 1 and 2. Annu Rev Pharmacol Toxicol 1998;38:97–120.</mixed-citation><mixed-citation xml:lang="ru">Vane J.R., Bakhle Y.S., Botting R.M. Cyclooxygenases 1 and 2. Annu Rev Pharmacol Toxicol 1998;38:97–120.</mixed-citation></citation-alternatives></ref><ref id="B16"><label>16.</label><citation-alternatives><mixed-citation xml:lang="en">16. DeWitt D.L., Meade E.A., Smith W.L. PGH synthase isoenzyme selectivity: the potential for safer nonsteroidal antiinflammatory drugs. Am J Med 1993;95(2A):40S–44S.</mixed-citation><mixed-citation xml:lang="ru">DeWitt D.L., Meade E.A., Smith W.L. PGH synthase isoenzyme selectivity: the potential for safer nonsteroidal antiinflammatory drugs. Am J Med 1993;95(2A):40S–44S.</mixed-citation></citation-alternatives></ref><ref id="B17"><label>17.</label><citation-alternatives><mixed-citation xml:lang="en">17. Taiwo Y.O., Levine J.D. Indomethacin blocks central nociceptive effects of PGF2 alpha. Brain Res 1986;373(1–2):81–4.</mixed-citation><mixed-citation xml:lang="ru">Taiwo Y.O., Levine J.D. Indomethacin blocks central nociceptive effects of PGF2 alpha. Brain Res 1986;373(1–2):81–4.</mixed-citation></citation-alternatives></ref><ref id="B18"><label>18.</label><citation-alternatives><mixed-citation xml:lang="en">18. Boie Y., Stocco R., Sawyer N. et al. Molecular cloning and characterization of the four rat prostaglandin E2 prostanoid receptor subtypes. Eur J Pharmacol 1997;340(2–3):227–41.</mixed-citation><mixed-citation xml:lang="ru">Boie Y., Stocco R., Sawyer N. et al. Molecular cloning and characterization of the four rat prostaglandin E2 prostanoid receptor subtypes. Eur J Pharmacol 1997;340(2–3):227–41.</mixed-citation></citation-alternatives></ref><ref id="B19"><label>19.</label><citation-alternatives><mixed-citation xml:lang="en">19. Marcus A.J. Transcellular metabolism of eicosanoids. Prog Hemost Thromb 1986;8:127–42.</mixed-citation><mixed-citation xml:lang="ru">Marcus A.J. Transcellular metabolism of eicosanoids. Prog Hemost Thromb 1986;8:127–42.</mixed-citation></citation-alternatives></ref><ref id="B20"><label>20.</label><citation-alternatives><mixed-citation xml:lang="en">20. Марусов И.В., Марусова И.Б., Игнатов Ю.Д. и др. Современные направления фармакологической коррекции эффектов липидных медиаторов воспаления: Научный обзор. Ученые записки СП(б)ГМУ им. акад. И.П. Павлова 2001;8(2):7–57.</mixed-citation><mixed-citation xml:lang="ru">Марусов И.В., Марусова И.Б., Игнатов Ю.Д. и др. Современные направления фармакологической коррекции эффектов липидных медиаторов воспаления: Научный обзор. Ученые записки СП(б)ГМУ им. акад. И.П. Павлова 2001;8(2):7–57.</mixed-citation></citation-alternatives></ref><ref id="B21"><label>21.</label><citation-alternatives><mixed-citation xml:lang="en">21. Brandão R.D., Veeck J., Van de Vijver K.K. et al. A randomised controlled phase II trial of pre-operative celecoxib treatment reveals anti- tumour transcriptional response in primary breast cancer. Breast Cancer Res 2013;15(2):R29.</mixed-citation><mixed-citation xml:lang="ru">Brandão R.D., Veeck J., Van de Vijver K.K. et al. A randomised controlled phase II trial of pre-operative celecoxib treatment reveals anti- tumour transcriptional response in primary breast cancer. Breast Cancer Res 2013;15(2):R29.</mixed-citation></citation-alternatives></ref><ref id="B22"><label>22.</label><citation-alternatives><mixed-citation xml:lang="en">22. Ma X., Holt D., Kundu N. et al. A prostaglandin E (PGE) receptor EP4 antagonist protects natural killer cells from PGE2-mediated immunosuppression and inhibits breast cancer metastasis. Oncoimmunology 2013;2(1):e22647.</mixed-citation><mixed-citation xml:lang="ru">Ma X., Holt D., Kundu N. et al. A prostaglandin E (PGE) receptor EP4 antagonist protects natural killer cells from PGE2-mediated immunosuppression and inhibits breast cancer metastasis. Oncoimmunology 2013;2(1):e22647.</mixed-citation></citation-alternatives></ref><ref id="B23"><label>23.</label><citation-alternatives><mixed-citation xml:lang="en">23. Bakhle Y.S. COX-2 and cancer: a new approach to an old problem. Br J Pharmacol 2001;134(6):1137–50.</mixed-citation><mixed-citation xml:lang="ru">Bakhle Y.S. COX-2 and cancer: a new approach to an old problem. Br J Pharmacol 2001;134(6):1137–50.</mixed-citation></citation-alternatives></ref><ref id="B24"><label>24.</label><citation-alternatives><mixed-citation xml:lang="en">24. Thun M.J., Henley S.J., Patrono C. Nonsteroidal anti-inflammatory drugs as anticancer agents: mechanistic, pharmacologic, and clinical issues. J Natl Cancer Inst 2002;94(4):252–66.</mixed-citation><mixed-citation xml:lang="ru">Thun M.J., Henley S.J., Patrono C. Nonsteroidal anti-inflammatory drugs as anticancer agents: mechanistic, pharmacologic, and clinical issues. J Natl Cancer Inst 2002;94(4):252–66.</mixed-citation></citation-alternatives></ref><ref id="B25"><label>25.</label><citation-alternatives><mixed-citation xml:lang="en">25. Gupta R.A., Dubois R.N. Colorectal cancer prevention and treatment by inhibition of cyclooxygenase-2. Nat Rev Cancer 2001;1(1):11–21.</mixed-citation><mixed-citation xml:lang="ru">Gupta R.A., Dubois R.N. Colorectal cancer prevention and treatment by inhibition of cyclooxygenase-2. Nat Rev Cancer 2001;1(1):11–21.</mixed-citation></citation-alternatives></ref><ref id="B26"><label>26.</label><citation-alternatives><mixed-citation xml:lang="en">26. Wang D., Mann J.R., DuBois R.N. The role of prostaglandins and other eicosanoids in the gastrointestinal tract. Gastroenterology 2005;128(5):1445–61.</mixed-citation><mixed-citation xml:lang="ru">Wang D., Mann J.R., DuBois R.N. The role of prostaglandins and other eicosanoids in the gastrointestinal tract. Gastroenterology 2005;128(5):1445–61.</mixed-citation></citation-alternatives></ref><ref id="B27"><label>27.</label><citation-alternatives><mixed-citation xml:lang="en">27. Masferrer J.L., Koki A., Seibert K. COX-2 inhibitors. A new class of angiogenic agents. Ann NY Acad Sci 1999;889:84–6.</mixed-citation><mixed-citation xml:lang="ru">Masferrer J.L., Koki A., Seibert K. COX-2 inhibitors. A new class of angiogenic agents. Ann NY Acad Sci 1999;889:84–6.</mixed-citation></citation-alternatives></ref><ref id="B28"><label>28.</label><citation-alternatives><mixed-citation xml:lang="en">28. Wang D., DuBios R.N. Cyclooxygenase 2-derived prostaglandin E2 regulates the angiogenic switch. Proc Natl Acad Sci USA 2004;101(2):415–6.</mixed-citation><mixed-citation xml:lang="ru">Wang D., DuBios R.N. Cyclooxygenase 2-derived prostaglandin E2 regulates the angiogenic switch. Proc Natl Acad Sci USA 2004;101(2):415–6.</mixed-citation></citation-alternatives></ref><ref id="B29"><label>29.</label><citation-alternatives><mixed-citation xml:lang="en">29. Khasar S.G., Gold M.S., Levine J.D. A tetrodotoxin - resistant sodium current mediates inflammatory pain in the rat. Neurosci Lett 1998;256(1):17–20.</mixed-citation><mixed-citation xml:lang="ru">Khasar S.G., Gold M.S., Levine J.D. A tetrodotoxin - resistant sodium current mediates inflammatory pain in the rat. Neurosci Lett 1998;256(1):17–20.</mixed-citation></citation-alternatives></ref><ref id="B30"><label>30.</label><citation-alternatives><mixed-citation xml:lang="en">30. Collins D.R., Davies S.N. Arachidonic acid metabolites and the synaptic potentiation evoked by activation of metabotropic glutamate receptors. Eur J Pharmacol 1998;342(2–3):213–6.</mixed-citation><mixed-citation xml:lang="ru">Collins D.R., Davies S.N. Arachidonic acid metabolites and the synaptic potentiation evoked by activation of metabotropic glutamate receptors. Eur J Pharmacol 1998;342(2–3):213–6.</mixed-citation></citation-alternatives></ref><ref id="B31"><label>31.</label><citation-alternatives><mixed-citation xml:lang="en">31. Cuzick J., Dowsett M., Pineda S. et al. Prognostic value of a combined estrogen receptor, progesterone receptor, Ki-67, and human epidermal growth factor receptor 2 immunohistochemical score and comparison with the genomic health recurrence score in early breast cancer. J Clin Oncol 2011;29(32):4273–8.</mixed-citation><mixed-citation xml:lang="ru">Cuzick J., Dowsett M., Pineda S. et al. Prognostic value of a combined estrogen receptor, progesterone receptor, Ki-67, and human epidermal growth factor receptor 2 immunohistochemical score and comparison with the genomic health recurrence score in early breast cancer. J Clin Oncol 2011;29(32):4273–8.</mixed-citation></citation-alternatives></ref><ref id="B32"><label>32.</label><citation-alternatives><mixed-citation xml:lang="en">32. Cho M.H., Yoon J.H., Jaegal Y.J. et al. Expression of cyclooxygenase-2 in breast carcinogenesis and its relation to HER-2/neu and p53 protein expression in invasive ductal carcinoma. Breast 2006;15(3):390–8.</mixed-citation><mixed-citation xml:lang="ru">Cho M.H., Yoon J.H., Jaegal Y.J. et al. Expression of cyclooxygenase-2 in breast carcinogenesis and its relation to HER-2/neu and p53 protein expression in invasive ductal carcinoma. Breast 2006;15(3):390–8.</mixed-citation></citation-alternatives></ref><ref id="B33"><label>33.</label><citation-alternatives><mixed-citation xml:lang="en">33. de Roos M.A., de Bock G.H., de Vries J. et al. p53 overexpression is a predictor of local recurrence after treatment for both in situ and invasive ductal carcinoma of the breast. J Surg Res 2007;140(1):109–14.</mixed-citation><mixed-citation xml:lang="ru">de Roos M.A., de Bock G.H., de Vries J. et al. p53 overexpression is a predictor of local recurrence after treatment for both in situ and invasive ductal carcinoma of the breast. J Surg Res 2007;140(1):109–14.</mixed-citation></citation-alternatives></ref><ref id="B34"><label>34.</label><citation-alternatives><mixed-citation xml:lang="en">34. Yiu G.K., Toker A. NFAT induces breast cancer cell invasion by promoting the induction of cyclooxygenase-2. J Biol Chem 2006;281(18):12210–7.</mixed-citation><mixed-citation xml:lang="ru">Yiu G.K., Toker A. NFAT induces breast cancer cell invasion by promoting the induction of cyclooxygenase-2. J Biol Chem 2006;281(18):12210–7.</mixed-citation></citation-alternatives></ref><ref id="B35"><label>35.</label><citation-alternatives><mixed-citation xml:lang="en">35. Howe L.R. Inflammation, breast cancer. Cyclooxygenase/prostaglandin signaling and breast cancer. Breast Cancer Res 2007;9(4):210.</mixed-citation><mixed-citation xml:lang="ru">Howe L.R. Inflammation, breast cancer. Cyclooxygenase/prostaglandin signaling and breast cancer. Breast Cancer Res 2007;9(4):210.</mixed-citation></citation-alternatives></ref><ref id="B36"><label>36.</label><citation-alternatives><mixed-citation xml:lang="en">36. Harvey J.M., Clark G.M., Osborne C.K., Allred D.C. Estrogen receptor status by immunohistochemistry is superior to the ligand-binding assay for predicting response to adjuvant endocrine therapy in breast cancer. J Clin Oncol 1999;17(5):1474–81.</mixed-citation><mixed-citation xml:lang="ru">Harvey J.M., Clark G.M., Osborne C.K., Allred D.C. Estrogen receptor status by immunohistochemistry is superior to the ligand-binding assay for predicting response to adjuvant endocrine therapy in breast cancer. J Clin Oncol 1999;17(5):1474–81.</mixed-citation></citation-alternatives></ref><ref id="B37"><label>37.</label><citation-alternatives><mixed-citation xml:lang="en">37. Kerlikowske K., Molinaro A.M., Gauthier M.L. et al. Biomarker expression and risk of subsequent tumors after initial ductal carcinoma in situ diagnosis. J Natl Cancer Inst 2010;102(9):627–37.</mixed-citation><mixed-citation xml:lang="ru">Kerlikowske K., Molinaro A.M., Gauthier M.L. et al. Biomarker expression and risk of subsequent tumors after initial ductal carcinoma in situ diagnosis. J Natl Cancer Inst 2010;102(9):627–37.</mixed-citation></citation-alternatives></ref><ref id="B38"><label>38.</label><citation-alternatives><mixed-citation xml:lang="en">38. Subbaramaiah K., Morris P.G., Zhou X.K. et al. Increased levels of COX-2 and prostaglandin E2 contribute to elevated aromatase expression in inflamed breast tissue of obese women. Cancer Discov 2012;2(4):356–65.</mixed-citation><mixed-citation xml:lang="ru">Subbaramaiah K., Morris P.G., Zhou X.K. et al. Increased levels of COX-2 and prostaglandin E2 contribute to elevated aromatase expression in inflamed breast tissue of obese women. Cancer Discov 2012;2(4):356–65.</mixed-citation></citation-alternatives></ref><ref id="B39"><label>39.</label><citation-alternatives><mixed-citation xml:lang="en">39. Wang D., DuBois R.N. The role of the PGE2-aromatase pathway in obesity- associated breast inflammation. Cancer Discov 2012;2(4):308–10.</mixed-citation><mixed-citation xml:lang="ru">Wang D., DuBois R.N. The role of the PGE2-aromatase pathway in obesity- associated breast inflammation. Cancer Discov 2012;2(4):308–10.</mixed-citation></citation-alternatives></ref><ref id="B40"><label>40.</label><citation-alternatives><mixed-citation xml:lang="en">40. Sandra N., Ester P., Marie-Agnès P. et al. The DHEA metabolite 7β-hydroxy- epiandrosterone exerts anti-estrogenic effects on breast cancer cell lines. Steroids 2012;77(5):542–51.</mixed-citation><mixed-citation xml:lang="ru">Sandra N., Ester P., Marie-Agnès P. et al. The DHEA metabolite 7β-hydroxy- epiandrosterone exerts anti-estrogenic effects on breast cancer cell lines. Steroids 2012;77(5):542–51.</mixed-citation></citation-alternatives></ref><ref id="B41"><label>41.</label><citation-alternatives><mixed-citation xml:lang="en">41. Wang J., Xiao X., Zhang Y. et al. Simultaneous modulation of COX-2, p300, Akt, and Apaf-1 signaling by melatonin to inhibit proliferation and induce apoptosis in breast cancer cells. J Pineal Res 2012;53(1):77–90.</mixed-citation><mixed-citation xml:lang="ru">Wang J., Xiao X., Zhang Y. et al. Simultaneous modulation of COX-2, p300, Akt, and Apaf-1 signaling by melatonin to inhibit proliferation and induce apoptosis in breast cancer cells. J Pineal Res 2012;53(1):77–90.</mixed-citation></citation-alternatives></ref><ref id="B42"><label>42.</label><citation-alternatives><mixed-citation xml:lang="en">42. Bronger H., Kraeft S., Schwarz-Boeger U. et al. Modulation of CXCR3 ligand secretion by prostaglandin E2 and cyclooxygenase inhibitors in human breast cancer. Breast Cancer Res 2012;14(1):R30.</mixed-citation><mixed-citation xml:lang="ru">Bronger H., Kraeft S., Schwarz-Boeger U. et al. Modulation of CXCR3 ligand secretion by prostaglandin E2 and cyclooxygenase inhibitors in human breast cancer. Breast Cancer Res 2012;14(1):R30.</mixed-citation></citation-alternatives></ref><ref id="B43"><label>43.</label><citation-alternatives><mixed-citation xml:lang="en">43. Holt D.M., Ma X., Kundu N. et al. Modulation of host natural killer cell functions in breast cancer via prostaglandin E2 receptors EP2 and EP4. J Immunother 2012;35(2):179–88.</mixed-citation><mixed-citation xml:lang="ru">Holt D.M., Ma X., Kundu N. et al. Modulation of host natural killer cell functions in breast cancer via prostaglandin E2 receptors EP2 and EP4. J Immunother 2012;35(2):179–88.</mixed-citation></citation-alternatives></ref><ref id="B44"><label>44.</label><citation-alternatives><mixed-citation xml:lang="en">44. Reader J., Holt D., Fulton A. Prostaglandin E2 EP receptors as therapeutic targets in breast cancer. Cancer Metastasis Rev 2011;30(3–4):449–63.</mixed-citation><mixed-citation xml:lang="ru">Reader J., Holt D., Fulton A. Prostaglandin E2 EP receptors as therapeutic targets in breast cancer. Cancer Metastasis Rev 2011;30(3–4):449–63.</mixed-citation></citation-alternatives></ref><ref id="B45"><label>45.</label><citation-alternatives><mixed-citation xml:lang="en">45. Gao X., Nawaz Z. Progesterone receptors – animal models and cell signaling in breast cancer role of steroid receptor coactivators and corepressors of progesterone receptors in breast cancer. Breast Cancer Res 2002;4(5):182–6.</mixed-citation><mixed-citation xml:lang="ru">Gao X., Nawaz Z. Progesterone receptors – animal models and cell signaling in breast cancer role of steroid receptor coactivators and corepressors of progesterone receptors in breast cancer. Breast Cancer Res 2002;4(5):182–6.</mixed-citation></citation-alternatives></ref><ref id="B46"><label>46.</label><citation-alternatives><mixed-citation xml:lang="en">46. Thill M., Hoellen F., Becker S. et al. Expression of prostaglandin- and vitamin D- metabolising enzymes in benign and malignant breast cells. Anticancer Res 2012;32(1):367–72.</mixed-citation><mixed-citation xml:lang="ru">Thill M., Hoellen F., Becker S. et al. Expression of prostaglandin- and vitamin D- metabolising enzymes in benign and malignant breast cells. Anticancer Res 2012;32(1):367–72.</mixed-citation></citation-alternatives></ref><ref id="B47"><label>47.</label><citation-alternatives><mixed-citation xml:lang="en">47. Xin X., Majumder M., Girish G.V. et al. Targeting COX-2 and EP4 to control tumor growth, angiogenesis, lymphangiogenesis and metastasis to the lungs and lymph nodes in a breast cancer model. Lab Invest 2012;92(8):1115–28.</mixed-citation><mixed-citation xml:lang="ru">Xin X., Majumder M., Girish G.V. et al. Targeting COX-2 and EP4 to control tumor growth, angiogenesis, lymphangiogenesis and metastasis to the lungs and lymph nodes in a breast cancer model. Lab Invest 2012;92(8):1115–28.</mixed-citation></citation-alternatives></ref><ref id="B48"><label>48.</label><citation-alternatives><mixed-citation xml:lang="en">48. Murata T., Aritake K., Matsumoto S. et al. Prostaglandin D2 is a mast cell-derived antiangiogenic factor in lung carcinoma. Proc Natl Acad Sci USA 2011;108(49):19802–7.</mixed-citation><mixed-citation xml:lang="ru">Murata T., Aritake K., Matsumoto S. et al. Prostaglandin D2 is a mast cell-derived antiangiogenic factor in lung carcinoma. Proc Natl Acad Sci USA 2011;108(49):19802–7.</mixed-citation></citation-alternatives></ref><ref id="B49"><label>49.</label><citation-alternatives><mixed-citation xml:lang="en">49. Murata T., Lin M.I., Aritake K. et al. Role of prostaglandin D2 receptor DP as a suppressor of tumor hyperpermeability and angiogenesis in vivo. Proc Natl Acad Sci USA 2008;105(50):20009–14.</mixed-citation><mixed-citation xml:lang="ru">Murata T., Lin M.I., Aritake K. et al. Role of prostaglandin D2 receptor DP as a suppressor of tumor hyperpermeability and angiogenesis in vivo. Proc Natl Acad Sci USA 2008;105(50):20009–14.</mixed-citation></citation-alternatives></ref><ref id="B50"><label>50.</label><citation-alternatives><mixed-citation xml:lang="en">50. Monroe D.G., McGee-Lawrence M.E., Oursler M.J., Westendorf J.J. Update on Wnt signaling in bone cell biology and bone disease. Gene. 2012;492(1):1–18.</mixed-citation><mixed-citation xml:lang="ru">Monroe D.G., McGee-Lawrence M.E., Oursler M.J., Westendorf J.J. Update on Wnt signaling in bone cell biology and bone disease. Gene. 2012;492(1):1–18.</mixed-citation></citation-alternatives></ref><ref id="B51"><label>51.</label><citation-alternatives><mixed-citation xml:lang="en">51. Ara T., Declerk Y.A. Interleukin-6 in bone metastasis and cancer progression. Eur J Cancer 2010;46(7):1223–31.</mixed-citation><mixed-citation xml:lang="ru">Ara T., Declerk Y.A. Interleukin-6 in bone metastasis and cancer progression. Eur J Cancer 2010;46(7):1223–31.</mixed-citation></citation-alternatives></ref><ref id="B52"><label>52.</label><citation-alternatives><mixed-citation xml:lang="en">52. Soto-Guzman A., Villegas-Comonfort S., Cortes-Reynosa P., Perez Salazar E. Role of arachidonic acid metabolism in Stat5 activation induced by oleic acid in MDA- MB-231 breast cancer cells. Prostaglandins Leukot Essent Fatty Acids 2013;88(3):243–9.</mixed-citation><mixed-citation xml:lang="ru">Soto-Guzman A., Villegas-Comonfort S., Cortes-Reynosa P., Perez Salazar E. Role of arachidonic acid metabolism in Stat5 activation induced by oleic acid in MDA- MB-231 breast cancer cells. Prostaglandins Leukot Essent Fatty Acids 2013;88(3):243–9.</mixed-citation></citation-alternatives></ref></ref-list></back></article>
