<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE root>
<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="other" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Cancer Urology</journal-id><journal-title-group><journal-title xml:lang="en">Cancer Urology</journal-title><trans-title-group xml:lang="ru"><trans-title>Онкоурология</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1726-9776</issn><issn publication-format="electronic">1996-1812</issn><publisher><publisher-name xml:lang="en">Publishing House ABV Press</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">236</article-id><article-id pub-id-type="doi">10.17650/1726-9776-2011-7-3-65-69</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>DIAGNOSIS AND TREATMENT OF URINARY SYSTEM TUMORS. RENAL CANCER</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ДИАГНОСТИКА И ЛЕЧЕНИЕ ОПУХОЛЕЙ МОЧЕПОЛОВОЙ СИСТЕМЫ. Рак почки</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">HUMAN PLASMA PROTEOME MAPPING IN HEALTH AND CLEAR CELL CARCINOMA OF THE KIDNEY</article-title><trans-title-group xml:lang="ru"><trans-title>КАРТИРОВАНИЕ ПРОТЕОМА ПЛАЗМЫ КРОВИ ЧЕЛОВЕКА В НОРМЕ И ПРИ СВЕТЛОКЛЕТОЧНОМ РАКЕ ПОЧКИ</trans-title></trans-title-group></title-group><contrib-group><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><email>sergekov@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Kovalev</surname><given-names>S. V.</given-names></name><name xml:lang="ru"><surname>Ковалев</surname><given-names>С. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>sergekov@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Yurchenko</surname><given-names>V. A.</given-names></name><name xml:lang="ru"><surname>Юрченко</surname><given-names>В. А.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>sergekov@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Matveev</surname><given-names>V. B.</given-names></name><name xml:lang="ru"><surname>Матвеев</surname><given-names>В. Б.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>sergekov@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Zaridze</surname><given-names>D. G.</given-names></name><name xml:lang="ru"><surname>Заридзе</surname><given-names>Д. Г.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>sergekov@mail.ru</email><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">РОНЦ им. Н.Н. Блохина РАМН, Москва</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2011-09-30" publication-format="electronic"><day>30</day><month>09</month><year>2011</year></pub-date><volume>7</volume><issue>3</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>65</fpage><lpage>69</lpage><history><date date-type="received" iso-8601-date="2014-08-03"><day>03</day><month>08</month><year>2014</year></date><date date-type="accepted" iso-8601-date="2014-08-03"><day>03</day><month>08</month><year>2014</year></date></history><permissions><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/></permissions><self-uri xlink:href="https://oncourology.abvpress.ru/oncur/article/view/236">https://oncourology.abvpress.ru/oncur/article/view/236</self-uri><abstract xml:lang="en"><p><bold/>Plasma proteome from patients with renal cell carcinoma (RCC) and controls underwent mass spectrometric mapping. A total of 247 proteins were identified; the expression of 12 proteins of them increased on transition from the controls to patients with Stages I–II and III–IV RCC. There was decreased expression of 14 proteins in this series. Out of the 26 proteins showing a change in their expressions, 7 proteins belong to acute-phase ones, 3 proteins are associated with the intercellular matrix. These proteins can be potential markers for RCC.</p></abstract><trans-abstract xml:lang="ru"><p>Проведено масс-спектрометрическое картирование протеома плазмы крови больных почечно-клеточным раком (ПКР) и конт-рольной группы. Идентифицировано 247 белков, из них экспрессия 12 белков увеличивалась при переходе от данных контрольной группы к анализам больным с I−II и III−IV стадиями заболевания. Снижение экспрессии в этом ряду показывали 14 белков. Из 26 протеинов, показавших изменение экспрессии, 7 относятся к белкам острой фазы, 3 белка связаны с межклеточным матриксом. Данные белки могут быть потенциальными маркерами ПКР.</p></trans-abstract><kwd-group xml:lang="en"><kwd>renal cell carcinoma</kwd><kwd>mass spectrometry</kwd><kwd>proteomic markers</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>почечно-клеточный рак</kwd><kwd>масс-спектрометрия</kwd><kwd>протеомные маркеры</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. Ljungberg B., Cowan N.C., Hanbury D.C. et al. EAU guidelines on renal cell carcinoma: the 2010 update. Eur Urol 2010;58:398–406.</mixed-citation><mixed-citation xml:lang="ru">Ljungberg B., Cowan N.C., Hanbury D.C. et al. EAU guidelines on renal cell carcinoma: the 2010 update. Eur Urol 2010;58:398–406.</mixed-citation></citation-alternatives></ref><ref id="B2"><label>2.</label><citation-alternatives><mixed-citation xml:lang="en">2. Chow W.H., Dong L.M., Devesa S.S. Epidemiology and risk factors for kidney cancer. Nature Reviews Urology 2010;7:245−57.</mixed-citation><mixed-citation xml:lang="ru">Chow W.H., Dong L.M., Devesa S.S. Epidemiology and risk factors for kidney cancer. Nature Reviews Urology 2010;7:245−57.</mixed-citation></citation-alternatives></ref><ref id="B3"><label>3.</label><citation-alternatives><mixed-citation xml:lang="en">3. Nickerson M.L., Jaeger E., Shi Y. et al. Improved identification of von Hippel-Lindau gene alternations in clear cell renal tumors. Clin Cancer Res 2008;14:4726–34.</mixed-citation><mixed-citation xml:lang="ru">Nickerson M.L., Jaeger E., Shi Y. et al. Improved identification of von Hippel-Lindau gene alternations in clear cell renal tumors. Clin Cancer Res 2008;14:4726–34.</mixed-citation></citation-alternatives></ref><ref id="B4"><label>4.</label><citation-alternatives><mixed-citation xml:lang="en">4. Заридзе Д.Г. Профилактика рака. М.: ИМА-ПРЕСС, 2009.</mixed-citation><mixed-citation xml:lang="ru">Заридзе Д.Г. Профилактика рака. М.: ИМА-ПРЕСС, 2009.</mixed-citation></citation-alternatives></ref><ref id="B5"><label>5.</label><citation-alternatives><mixed-citation xml:lang="en">5. Perroud B., Lee J., Valkova N. et al. Pathway analysis of kidney cancer using proteomics and metabolic profiling. Mol Cancer 2006;5:64−81.</mixed-citation><mixed-citation xml:lang="ru">Perroud B., Lee J., Valkova N. et al. Pathway analysis of kidney cancer using proteomics and metabolic profiling. Mol Cancer 2006;5:64−81.</mixed-citation></citation-alternatives></ref><ref id="B6"><label>6.</label><citation-alternatives><mixed-citation xml:lang="en">6. Craven R.A., Stanley A.J., Hanrahan S. et al. Proteomic analysis of primary cell lines identifies protein changes present in renal cell carcinoma. Proteomics 2006;6:2853–64.</mixed-citation><mixed-citation xml:lang="ru">Craven R.A., Stanley A.J., Hanrahan S. et al. Proteomic analysis of primary cell lines identifies protein changes present in renal cell carcinoma. Proteomics 2006;6:2853–64.</mixed-citation></citation-alternatives></ref><ref id="B7"><label>7.</label><citation-alternatives><mixed-citation xml:lang="en">7. Banks R.E., Craven R.A., Harnden P. et al. Key clinical issues in renal cancer: a challenge for proteomics. World J Urol 2007;25:537–56.</mixed-citation><mixed-citation xml:lang="ru">Banks R.E., Craven R.A., Harnden P. et al. Key clinical issues in renal cancer: a challenge for proteomics. World J Urol 2007;25:537–56.</mixed-citation></citation-alternatives></ref><ref id="B8"><label>8.</label><citation-alternatives><mixed-citation xml:lang="en">8. Opatrná S., Chiangjong W., Korabecná M. et al. Plasma proteome profiling of von Hippel-Lindau disease after total and subtotal nephrectomy: a preliminary study. Clin Biochem 2010;43:142−9.</mixed-citation><mixed-citation xml:lang="ru">Opatrná S., Chiangjong W., Korabecná M. et al. Plasma proteome profiling of von Hippel-Lindau disease after total and subtotal nephrectomy: a preliminary study. Clin Biochem 2010;43:142−9.</mixed-citation></citation-alternatives></ref><ref id="B9"><label>9.</label><citation-alternatives><mixed-citation xml:lang="en">9. Eichelberg C., Junker K., Ljungberg B. et al. Diagnostic and prognostic molecular markers for renal cell carcinoma: a critical appraisal of the current state of research and clinical applicability. Eur Urol 2009;55:851–63.</mixed-citation><mixed-citation xml:lang="ru">Eichelberg C., Junker K., Ljungberg B. et al. Diagnostic and prognostic molecular markers for renal cell carcinoma: a critical appraisal of the current state of research and clinical applicability. Eur Urol 2009;55:851–63.</mixed-citation></citation-alternatives></ref><ref id="B10"><label>10.</label><citation-alternatives><mixed-citation xml:lang="en">10. Janech M.G., Raymond J.R., Arthur J.M. Proteomics in renal research. Am J Physiol Renal Physiol 2007;292:F501–F512.</mixed-citation><mixed-citation xml:lang="ru">Janech M.G., Raymond J.R., Arthur J.M. Proteomics in renal research. Am J Physiol Renal Physiol 2007;292:F501–F512.</mixed-citation></citation-alternatives></ref><ref id="B11"><label>11.</label><citation-alternatives><mixed-citation xml:lang="en">11. http://www.chem.agilent.com/Library/usermanuals/Public/5969-1597.pdf</mixed-citation><mixed-citation xml:lang="ru">http://www.chem.agilent.com/Library/usermanuals/Public/5969-1597.pdf</mixed-citation></citation-alternatives></ref><ref id="B12"><label>12.</label><citation-alternatives><mixed-citation xml:lang="en">12. http://www.chem.agilent.com/Library/usermanuals/Public/G2458-90003_SamplePrepGuide_online.pdf P. 67 77.</mixed-citation><mixed-citation xml:lang="ru">http://www.chem.agilent.com/Library/usermanuals/Public/G2458-90003_SamplePrepGuide_online.pdf P. 67 77.</mixed-citation></citation-alternatives></ref><ref id="B13"><label>13.</label><citation-alternatives><mixed-citation xml:lang="en">13. Martosella J., Zolotarjova N., Liu H. et al. Reversed-phase high-performance liquid chromatographic prefractionation of immunodepleted human serum proteins to enhance mass spectrometry identification of lower-abundant proteins. J Proteome Res 2005;4:1522−37.</mixed-citation><mixed-citation xml:lang="ru">Martosella J., Zolotarjova N., Liu H. et al. Reversed-phase high-performance liquid chromatographic prefractionation of immunodepleted human serum proteins to enhance mass spectrometry identification of lower-abundant proteins. J Proteome Res 2005;4:1522−37.</mixed-citation></citation-alternatives></ref><ref id="B14"><label>14.</label><citation-alternatives><mixed-citation xml:lang="en">14. www.hppp.org</mixed-citation><mixed-citation xml:lang="ru">www.hppp.org</mixed-citation></citation-alternatives></ref><ref id="B15"><label>15.</label><citation-alternatives><mixed-citation xml:lang="en">15. Saito K., Tatokoro M., Fujii Y. et al. Impact of C-reactive protein kinetics on survival of patients with metastatic renal cell carcinoma. Eur Urol 2009;55:1145–54.</mixed-citation><mixed-citation xml:lang="ru">Saito K., Tatokoro M., Fujii Y. et al. Impact of C-reactive protein kinetics on survival of patients with metastatic renal cell carcinoma. Eur Urol 2009;55:1145–54.</mixed-citation></citation-alternatives></ref><ref id="B16"><label>16.</label><citation-alternatives><mixed-citation xml:lang="en">16. Markiewski M.M., Lambris J.D. Is complement good or bad for cancer patients? A new perspective on an old dilemma. Trends Immunol 2009;30:286−92.</mixed-citation><mixed-citation xml:lang="ru">Markiewski M.M., Lambris J.D. Is complement good or bad for cancer patients? A new perspective on an old dilemma. Trends Immunol 2009;30:286−92.</mixed-citation></citation-alternatives></ref><ref id="B17"><label>17.</label><citation-alternatives><mixed-citation xml:lang="en">17. Sadrzadeh S.M., Bozorgmehr J. Haptoglobin phenotypes in health and disorders. Am J Clin Pathol 2004;121(Suppl):97−104.</mixed-citation><mixed-citation xml:lang="ru">Sadrzadeh S.M., Bozorgmehr J. Haptoglobin phenotypes in health and disorders. Am J Clin Pathol 2004;121(Suppl):97−104.</mixed-citation></citation-alternatives></ref><ref id="B18"><label>18.</label><citation-alternatives><mixed-citation xml:lang="en">18. Karpova M.A., Moshkovskii S.A., Toropygin I.Y. et al. Cancer-specific MALDI-TOF profiles of blood serum and plasma: biological meaning and perspectives. J Proteomics 2010;73:537−51.</mixed-citation><mixed-citation xml:lang="ru">Karpova M.A., Moshkovskii S.A., Toropygin I.Y. et al. Cancer-specific MALDI-TOF profiles of blood serum and plasma: biological meaning and perspectives. J Proteomics 2010;73:537−51.</mixed-citation></citation-alternatives></ref><ref id="B19"><label>19.</label><citation-alternatives><mixed-citation xml:lang="en">19. Tolson J., Bogumil R., Brunst E. et al. Serum protein profiling by SELDI mass spectrometry: detection of multiple variants of serum amyloid alpha in renal cancer patients. Lab Invest 2004;84:1220–1.</mixed-citation><mixed-citation xml:lang="ru">Tolson J., Bogumil R., Brunst E. et al. Serum protein profiling by SELDI mass spectrometry: detection of multiple variants of serum amyloid alpha in renal cancer patients. Lab Invest 2004;84:1220–1.</mixed-citation></citation-alternatives></ref><ref id="B20"><label>20.</label><citation-alternatives><mixed-citation xml:lang="en">20. Ramankulov A., Lein M., Johannsen M. et al. Serum amyloid A as indicator of distant metastases but not as early tumor marker in patients with renal cell carcinoma. Cancer Lett 2008;269:85−92.</mixed-citation><mixed-citation xml:lang="ru">Ramankulov A., Lein M., Johannsen M. et al. Serum amyloid A as indicator of distant metastases but not as early tumor marker in patients with renal cell carcinoma. Cancer Lett 2008;269:85−92.</mixed-citation></citation-alternatives></ref><ref id="B21"><label>21.</label><citation-alternatives><mixed-citation xml:lang="en">21. Meyer H.A., Tulle A., Jung M. et al. Identification of stanniocalcin 2 as prognostic marker in renal cell carcinoma. Eur Urol 2009;55:669–78.</mixed-citation><mixed-citation xml:lang="ru">Meyer H.A., Tulle A., Jung M. et al. Identification of stanniocalcin 2 as prognostic marker in renal cell carcinoma. Eur Urol 2009;55:669–78.</mixed-citation></citation-alternatives></ref><ref id="B22"><label>22.</label><citation-alternatives><mixed-citation xml:lang="en">22. Reichle A., Grassinger J., Bross K. et al. C-reactive protein in patients with metastatic clear cell renal carcinoma: an important biomarker for tumor-associated inflammation. Biomark Insights 2007;1:87–98.</mixed-citation><mixed-citation xml:lang="ru">Reichle A., Grassinger J., Bross K. et al. C-reactive protein in patients with metastatic clear cell renal carcinoma: an important biomarker for tumor-associated inflammation. Biomark Insights 2007;1:87–98.</mixed-citation></citation-alternatives></ref><ref id="B23"><label>23.</label><citation-alternatives><mixed-citation xml:lang="en">23. Zeng Z., Hincapie M., Haab B.B. et al. The development of an integrated platform to identify breast cancer glycoproteome changes in human serum. J Chromatogr A 2010;1217:3307−15.</mixed-citation><mixed-citation xml:lang="ru">Zeng Z., Hincapie M., Haab B.B. et al. The development of an integrated platform to identify breast cancer glycoproteome changes in human serum. J Chromatogr A 2010;1217:3307−15.</mixed-citation></citation-alternatives></ref><ref id="B24"><label>24.</label><citation-alternatives><mixed-citation xml:lang="en">24. Kreunin P., Zhao J., Rosser C. et al. Bladder cancer associated glycoprotein signatures revealed by urinary proteomic profiling. J Proteome Res 2007;6:2631−9.</mixed-citation><mixed-citation xml:lang="ru">Kreunin P., Zhao J., Rosser C. et al. Bladder cancer associated glycoprotein signatures revealed by urinary proteomic profiling. J Proteome Res 2007;6:2631−9.</mixed-citation></citation-alternatives></ref><ref id="B25"><label>25.</label><citation-alternatives><mixed-citation xml:lang="en">25. Alvarez-Chaver P., Rodriguez-Piсeiro A.M., Rodriguez-Berrocal F.J. et al. Identification of hydrophobic proteins as biomarker candidates for colorectal cancer. Int J Biochem Cell Biol 2007;39:529−40.</mixed-citation><mixed-citation xml:lang="ru">Alvarez-Chaver P., Rodriguez-Piсeiro A.M., Rodriguez-Berrocal F.J. et al. Identification of hydrophobic proteins as biomarker candidates for colorectal cancer. Int J Biochem Cell Biol 2007;39:529−40.</mixed-citation></citation-alternatives></ref><ref id="B26"><label>26.</label><citation-alternatives><mixed-citation xml:lang="en">26. Cervi D., Pak B., Venier Н.L. et al. Micronutrients attenuate progression of prostate cancer by elevating the endogenous inhibitor of angiogenesis, platelet factor-4. BMC Cancer 2010;10:258-258.</mixed-citation><mixed-citation xml:lang="ru">Cervi D., Pak B., Venier Н.L. et al. Micronutrients attenuate progression of prostate cancer by elevating the endogenous inhibitor of angiogenesis, platelet factor-4. BMC Cancer 2010;10:258-258.</mixed-citation></citation-alternatives></ref><ref id="B27"><label>27.</label><citation-alternatives><mixed-citation xml:lang="en">27. Fiedler G.M., Leichtle A.B., Kase J. et al. Serum peptidome profiling revealed platelet factor 4 as a potential discriminating Peptide associated with pancreatic cancer. Clin Cancer Res 2009;15:3812−9.</mixed-citation><mixed-citation xml:lang="ru">Fiedler G.M., Leichtle A.B., Kase J. et al. Serum peptidome profiling revealed platelet factor 4 as a potential discriminating Peptide associated with pancreatic cancer. Clin Cancer Res 2009;15:3812−9.</mixed-citation></citation-alternatives></ref><ref id="B28"><label>28.</label><citation-alternatives><mixed-citation xml:lang="en">28. Cervi D., Yip T.-T., Bhattacharya N. et al. Platelet-associated PF-4 as a biomarker of early tumor growth. Blood 2008;111:1201−7.</mixed-citation><mixed-citation xml:lang="ru">Cervi D., Yip T.-T., Bhattacharya N. et al. Platelet-associated PF-4 as a biomarker of early tumor growth. Blood 2008;111:1201−7.</mixed-citation></citation-alternatives></ref><ref id="B29"><label>29.</label><citation-alternatives><mixed-citation xml:lang="en">29. Feldmann G., Mishra A., Hong S.M. et al. Inhibiting the cyclin-dependent kinase CDK5 blocks pancreatic cancer formation and progression through the suppression of Ras-Ral signaling. Cancer Res 2010;70:4460−9.</mixed-citation><mixed-citation xml:lang="ru">Feldmann G., Mishra A., Hong S.M. et al. Inhibiting the cyclin-dependent kinase CDK5 blocks pancreatic cancer formation and progression through the suppression of Ras-Ral signaling. Cancer Res 2010;70:4460−9.</mixed-citation></citation-alternatives></ref><ref id="B30"><label>30.</label><citation-alternatives><mixed-citation xml:lang="en">30. Upadhyay A.K., Ajay A.K., Singh S. et al. Cell cycle regulatory protein 5 (Cdk5) is a novel downstream target of ERK in carboplatin induced death of breast cancer cells. Curr Cancer Drug Targets 2008;8:741−52.</mixed-citation><mixed-citation xml:lang="ru">Upadhyay A.K., Ajay A.K., Singh S. et al. Cell cycle regulatory protein 5 (Cdk5) is a novel downstream target of ERK in carboplatin induced death of breast cancer cells. Curr Cancer Drug Targets 2008;8:741−52.</mixed-citation></citation-alternatives></ref><ref id="B31"><label>31.</label><citation-alternatives><mixed-citation xml:lang="en">31. Haiman M., Salvenmoser W., Scheiber K. et al. Immunohistochemical localization of apolipoprotein A-IV in human kidney tissue. Kidney Int 2005;68:1130–6.</mixed-citation><mixed-citation xml:lang="ru">Haiman M., Salvenmoser W., Scheiber K. et al. Immunohistochemical localization of apolipoprotein A-IV in human kidney tissue. Kidney Int 2005;68:1130–6.</mixed-citation></citation-alternatives></ref><ref id="B32"><label>32.</label><citation-alternatives><mixed-citation xml:lang="en">32. Hall A.K. Amplification-independent overexpression of thymosin beta-10 mRNA in human renal cell carcinoma. Ren Fail 1994;16:243−54.</mixed-citation><mixed-citation xml:lang="ru">Hall A.K. Amplification-independent overexpression of thymosin beta-10 mRNA in human renal cell carcinoma. Ren Fail 1994;16:243−54.</mixed-citation></citation-alternatives></ref><ref id="B33"><label>33.</label><citation-alternatives><mixed-citation xml:lang="en">33. Sparvero L.J., Asafu-Adjei D., Kang R. et al. RAGE (Receptor for Advanced Glycation Endproducts), RAGE ligands, and their role in cancer and inflammation. J Transl Med 2009;7:7−17.</mixed-citation><mixed-citation xml:lang="ru">Sparvero L.J., Asafu-Adjei D., Kang R. et al. RAGE (Receptor for Advanced Glycation Endproducts), RAGE ligands, and their role in cancer and inflammation. J Transl Med 2009;7:7−17.</mixed-citation></citation-alternatives></ref><ref id="B34"><label>34.</label><citation-alternatives><mixed-citation xml:lang="en">34. Liang X., Huuskonen J., Hajivandi M. et al. Identification and quantification of proteins differentially secreted by a pair of normal and malignant breast-cancer cell lines. Proteomics 2009;9:182−93.</mixed-citation><mixed-citation xml:lang="ru">Liang X., Huuskonen J., Hajivandi M. et al. Identification and quantification of proteins differentially secreted by a pair of normal and malignant breast-cancer cell lines. Proteomics 2009;9:182−93.</mixed-citation></citation-alternatives></ref><ref id="B35"><label>35.</label><citation-alternatives><mixed-citation xml:lang="en">35. Forstenberger G., Senn E., Morant R. et al. Serum levels of IGF-1 and IGFBP-3 during adjuvant chemotherapy for primary breast cancer. Breast 2006;15:64−8.</mixed-citation><mixed-citation xml:lang="ru">Forstenberger G., Senn E., Morant R. et al. Serum levels of IGF-1 and IGFBP-3 during adjuvant chemotherapy for primary breast cancer. Breast 2006;15:64−8.</mixed-citation></citation-alternatives></ref></ref-list></back></article>
