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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">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">949</article-id><article-id pub-id-type="doi">10.17650/1726-9776-2019-15-3-132-142</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>REVIEW</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ОБЗОР</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">KIM-1 as a potential serological/urinological tumor-associated marker of renal cell carcinoma and chemotherapy nephrotoxicity</article-title><trans-title-group xml:lang="ru"><trans-title>KIM-1 (kidney injury molecule-1) как потенциальный серологический/урологический опухолеассоциированный маркер почечно-клеточного рака и нефротоксичности химиопрепаратов</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-0676-600X</contrib-id><name-alternatives><name xml:lang="en"><surname>Solokhina</surname><given-names>M. P.</given-names></name><name xml:lang="ru"><surname>Солохина</surname><given-names>М. П.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p><italic>3 2nd Botkinskiy Proezd, Moscow 125284</italic></p></bio><bio xml:lang="ru"><p><bold>Мариям Павловна Салохина,</bold> отделение Прогноза, научный сотрудник</p><p><italic>125284 Москва, 2-й Боткинский проезд, 3</italic></p><p>SPIN: 5341-9803</p></bio><email>solomar59@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-7406-9973</contrib-id><name-alternatives><name xml:lang="en"><surname>Sergeeva</surname><given-names>N. S.</given-names></name><name xml:lang="ru"><surname>Сергеева</surname><given-names>Н. С.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p><italic>3 2nd Botkinskiy Proezd, Moscow 125284, </italic></p><p><italic>1 Ostrovityanova St., Moscow 117997</italic></p></bio><bio xml:lang="ru"><p><bold>Наталья Сергеевна Сергеева</bold></p><p><italic>117997 Москва, ул. Островитянова, 1, </italic></p><p><italic>125284 Москва, 2-й Боткинский проезд, 3</italic></p><p><bold/></p></bio><email>prognoz.01@mail.ru</email><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-2997-4936</contrib-id><name-alternatives><name xml:lang="en"><surname>Marshutina</surname><given-names>N. V.</given-names></name><name xml:lang="ru"><surname>Маршутина</surname><given-names>Н. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p><italic>3 2nd Botkinskiy Proezd, Moscow 125284</italic></p></bio><bio xml:lang="ru"><p><bold>Нина Викторовна Маршутина </bold></p><p><italic>125284 Москва, 2-й Боткинский проезд, 3</italic></p><p><bold/></p></bio><email>nin.mars@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-5920-5823</contrib-id><name-alternatives><name xml:lang="en"><surname>Alentov</surname><given-names>I. I.</given-names></name><name xml:lang="ru"><surname>Алентов</surname><given-names>И. И.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p><italic>3 2nd Botkinskiy Proezd, Moscow 125284</italic></p></bio><bio xml:lang="ru"><p><bold>Игорь Игоревич Алентов </bold></p><p><italic>125284 Москва, 2-й Боткинский проезд, 3</italic></p><p><bold/></p></bio><email>igor@pushkino.tv</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Kanukoev</surname><given-names>K. Yu.</given-names></name><name xml:lang="ru"><surname>Канукоев</surname><given-names>К. Ю.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p><italic>3 2nd Botkinskiy Proezd, Moscow 125284</italic></p></bio><bio xml:lang="ru"><p><bold>Кантемир Юрьевич Канукоев </bold></p><p><italic>125284 Москва, 2-й Боткинский проезд, 3</italic></p><p><bold/></p></bio><email>kan12390@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-4171-6211</contrib-id><name-alternatives><name xml:lang="en"><surname>Nyushko</surname><given-names>K. M.</given-names></name><name xml:lang="ru"><surname>Нюшко</surname><given-names>К. М.</given-names></name></name-alternatives><bio xml:lang="en"><p><italic>3 2nd Botkinskiy Proezd, Moscow 125284</italic></p></bio><bio xml:lang="ru"><p><bold>Кирилл <bold>Нюшко Михайлович </bold>Нюшко </bold></p><p><italic>125284 Москва, 2-й Боткинский проезд, 3</italic></p><p><bold/></p></bio><email>kirandja@yandex.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-1353-2271</contrib-id><name-alternatives><name xml:lang="en"><surname>Alekseev</surname><given-names>B. Ya.</given-names></name><name xml:lang="ru"><surname>Алексеев</surname><given-names>Б. Я.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p><italic>3 2nd Botkinskiy Proezd, Moscow 125284</italic></p></bio><bio xml:lang="ru"><p><bold>Борис Яковлевич Алексеев </bold></p><p><italic>125284 Москва, 2-й Боткинский проезд, 3</italic></p><p><bold/></p></bio><email>byalekseev@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-8784-8415</contrib-id><name-alternatives><name xml:lang="en"><surname>Kaprin</surname><given-names>A. D.</given-names></name><name xml:lang="ru"><surname>Каприн</surname><given-names>А. Д.</given-names></name></name-alternatives><bio xml:lang="en"><p><italic>3 2nd Botkinskiy Proezd, Moscow 125284</italic></p></bio><bio xml:lang="ru"><p><bold>Андрей Дмитриевич Каприн </bold></p><p><italic>125284 Москва, 2-й Боткинский проезд, 3</italic></p><p><bold/></p></bio><email>kaprin@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">National Medical Research Radiological Center, Ministry of Health of Russia</institution></aff><aff><institution xml:lang="ru">ФГБУ «Национальный медицинский исследовательский центр радиологии» Минздрава России</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">N.I. Pirogov Russian National Research Medical University, Ministry of Health of Russia</institution></aff><aff><institution xml:lang="ru">ФГБОУ ВО «Российский национальный исследовательский медицинский университет им. Н.И. Пирогова» Минздрава России</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2019-09-30" publication-format="electronic"><day>30</day><month>09</month><year>2019</year></pub-date><volume>15</volume><issue>3</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>132</fpage><lpage>142</lpage><history><date date-type="received" iso-8601-date="2019-04-30"><day>30</day><month>04</month><year>2019</year></date><date date-type="accepted" iso-8601-date="2019-06-14"><day>14</day><month>06</month><year>2019</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/949">https://oncourology.abvpress.ru/oncur/article/view/949</self-uri><abstract xml:lang="en"><p>The last decades are characterized by an active search for highly sensitive and specific urinological and serological tumor-associated markers of renal cell carcinoma. This review analyses the results of studies of traditional serological tumor-associated markers and a potential new tumor-associated marker of renal cell carcinoma: kidney injury molecule-1, or KIM-1. The structure, sources and functions of KIM-1 in normal conditions and in damaged renal tubules, its potential role in carcinogenesis are described. The experience of using KIM-1 for specifying diagnosis of the most common histological types of renal cell carcinoma is analyzed. Data on KIM-1 expression in malignant tumors in other locations and non-oncological kidney disorders are presented. The role of KIM-1 in early diagnosis of nephrotoxic effect of antitumor drugs is described. The accumulated data is promising in regards to using KIM-1 in clinical oncology as a urinological and serological marker of renal cell carcinoma and chemotherapy nephrotoxicity.</p></abstract><trans-abstract xml:lang="ru"><p>Последние десятилетия активно ведутся поиски высокочувствительных и специфичных уринологических и серологических опухолеассоциированных маркеров (ОМ) для почечно-клеточного рака (ПКР). В обзоре проведен анализ результатов исследования традиционных серологических ОМ и нового потенциального ОМ для ПКР – молекулы повреждения почек-1 (kidney injury molecule-1 - KIM-1). Описаны структура, источники и функции KIM-1 в норме и при повреждении почечных канальцев, его возможная роль в канцерогенезе. Проанализирован опыт использования KIM-1 в уточняющей диагностике наиболее распространенных гистологических типов ПКР. Представлены данные, касающиеся экспрессии KIM-1 при злокачественных новообразованиях других локализаций и при заболеваниях почек неонкологического генеза. Показана роль KIM-1 в ранней диагностике нефротоксичного действия противоопухолевых препаратов. Накопленные данные открывают перспективы использования KIM-1 в клинической онкологии как уринологического и серологического маркера ПКР и нефротоксичности химиотерапии.</p></trans-abstract><kwd-group xml:lang="en"><kwd>renal cell carcinoma</kwd><kwd>tumor-associated marker</kwd><kwd>KIM-1</kwd><kwd>kidney disorder</kwd><kwd>chemotherapy nephrotoxicity</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>почечно-клеточный рак</kwd><kwd>опухолеассоциированные маркеры</kwd><kwd>KIM-1</kwd><kwd>заболевания почек</kwd><kwd>нефротоксичность химиотерапии</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">State of oncological care in Russia in 2017. Eds.: А.D. Kaprin, V.V. Starinskiy, G.V. Petrova. Moscow: MNIOI im. P.A. Gertsena – filial FGBU “NMIRTS radiologii” Minzdrava Rossii, 2018. 236 p. (In Russ.).</mixed-citation><mixed-citation xml:lang="ru">Состояние онкологической помощи населению России в 2017 году. Под ред. А.Д. Каприна, В.В. Старинского, Г.В. Петровой. М.: МНИОИ им. П.А. Герцена – филиал ФГБУ «НМИЦ радиологии» Минздрава России, 2018. 236 с.</mixed-citation></citation-alternatives></ref><ref id="B2"><label>2.</label><mixed-citation>Grankvist K., Ljungberg B., Rasmuson T. Evaluation of five glycoprotein tumour markers (CEA, CA-50, CA-19-9, CA-125, CA-15-3) for the prognosis of renal-cell carcinoma. Int J Cancer 1997;74(2):233–6. DOI: 10.1002/(SICI)10970215(19970422)74:2&lt;233::AIDIJC17&gt;3.0.CO;2-E.</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Jacobsen J., Rasmuson T., Grankvist K., Ljungberg B. Vascular endothelial growth factor as prognostic factor in renal cell carcinoma. J Urol 2000;163(1):343–7. DOI: 10.1097/00005392-20000100000092.</mixed-citation></ref><ref id="B4"><label>4.</label><citation-alternatives><mixed-citation xml:lang="en">Banyra O.B., Stroy A.A., Shulyak A.V. Tumor markers in kidney cancer diagnosing. Eksperimental’naya i klinicheskaya urologiya = Experimental and Clinical Urology 2011;4:72–8. (In Russ.).</mixed-citation><mixed-citation xml:lang="ru">Баныра О.Б., Строй А.А., Шуляк А.В. Маркеры опухолевого роста в диагностике рака почки. Экспериментальная и клиническая урология 2011;4:72–8.</mixed-citation></citation-alternatives></ref><ref id="B5"><label>5.</label><mixed-citation>Hotakainen K., Ljungberg B., Paju A. et al. The free β-subunit of human chorionic gonadotropin as a prognostic factor in renal cell carcinoma. Br J Cancer 2002;86(2):185–9. DOI: 10.1038/sj.bjc.6600050.</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>Stenman U., Paju A., Jakobsen A. Prognostic significance of tumor-associated trypsin inhibitor in renal cell carcinoma. Libro de Abstracts. 2001;125.</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>Zurita A.J., Jonasch E., Wang X. et al. A cytokine and angiogenic factor (CAF) analysis in plasma for selection of sorafenib therapy in patients with metastatic renal cell carcinoma. Ann Oncol 2012;23(1):46–52. DOI: 10.1093/annonc/mdr047.</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>Escudier B., Eisen T., Stadler W.M. et al. Sorafenib for treatment of renal cell carcinoma: final efficacy and safety results of the phase III treatment approaches in renal cancer global evaluation trial. J Clin Oncol 2009;27(20):3312–8. DOI: 10.1200/JCO.2008.19.5511.</mixed-citation></ref><ref id="B9"><label>9.</label><citation-alternatives><mixed-citation xml:lang="en">Sergeeva N.S., Rusakov I.G., Marshutina N.V. et al. Examination of a serological tumor marker Tu M2-PK in patients with renal carcinoma. Rossiyskiy onkologicheskiy zhurnal = Russian Journal of Oncology 2005;3:30–2. (In Russ.).</mixed-citation><mixed-citation xml:lang="ru">Сергеева Н.С., Русаков И.Г., Маршутина Н.В. и др. Исследование нового метаболического опухолевого маркера Tu M2-PK при раке почки. Российский онкологический журнал 2005;3:30–2.</mixed-citation></citation-alternatives></ref><ref id="B10"><label>10.</label><mixed-citation>Wechsel H.W., Petri E., Bichler K.H., Feil G. Marker for renal cell carcinoma (RCC): the dimeric form of pyruvate kinase type M2 (Tu M2-PK). Anticancer Res 1999;19(4A):2583–90.</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>Su Kim D., Choi Y.D., Moon M. et al. Composite Three-marker assay for early detection of kidney cancer. Cancer Epidemiol Biomarkers Prev 2013;22(3):390–8. DOI: 10.1158/1055-9965.EPI-12-1156.</mixed-citation></ref><ref id="B12"><label>12.</label><citation-alternatives><mixed-citation xml:lang="en">Klyuchagina Yu.I., Sokolova Z.A., Baryshnikova M.A. Role of PD-1 receptor and its ligands PD-L1 and PD-L2 in cancer immunotherapy. Onkopediatriya = Oncopediatrics 2017;4(1):49–55. (In Russ.). DOI: 10.15690/опоо.у4И.1684.</mixed-citation><mixed-citation xml:lang="ru">Ключагина Ю.И., Соколова З.А., Барышникова М.А. Роль рецептора PD-1 и его лигандов PD-L1 и PD-L2 в иммунотерапии опухолей. Онкопедиатрия 2017;4(1):49–55. DOI: 10.15690/опоо.у4И.1684.</mixed-citation></citation-alternatives></ref><ref id="B13"><label>13.</label><citation-alternatives><mixed-citation xml:lang="en">Kushlinskiy N.E., Gershtein E.S., Morozov A.A. et al. Soluble ligand of the immune control point receptor (sPD-Ll) in serum in renal cell carcinoma. Byulleten’ eksperimental’noy biologii i meditsiny = Bulletin of experimental biology and medicine 2018; 166(9):325–9. (In Russ.).</mixed-citation><mixed-citation xml:lang="ru">Кушлинский Н.Е., Герштейн Е.С., Морозов А.А. и др. Растворимый лиганд рецептора контрольной точки иммунитета (sPD-Ll) в сыворотке крови при почечноклеточном раке. Бюллетень экспериментальной биологии и медицины 2018;166(9):325–9.</mixed-citation></citation-alternatives></ref><ref id="B14"><label>14.</label><mixed-citation>Zhang W., Ni M., Su Y. et al. MicroRNAs in serum exosomes as potential biomarkers in clear-cell renal cell carcinoma. Eur Urol Focus 2018;4(3):412–9. DOI: 10.1016/j.euf.2016.09.007.</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>Scelo G., Muller D.C., Riboli E. et al. KIM1 as a blood-based marker for early detection of kidney cancer: a prospective nested casecontrol study. Clin Cancer Res 2018;24(22):5594–601. DOI: 10.1158/10780432.CCR-18-1496.</mixed-citation></ref><ref id="B16"><label>16.</label><mixed-citation>Han W.K., Alinani A., Wu C.L. et al. Human kidney injury molecule-1 is a tissue and urinary tumor marker of renal cell carcinoma. J Am Soc Nephrol 2005;16(4):1126–34. DOI: 10.1681/ASN.2004070530.</mixed-citation></ref><ref id="B17"><label>17.</label><mixed-citation>Bailly V., Zhang Z., Meier W. et al. Shedding of kidney injury molecule-1, a putative adhesion protein involved in renal regeneration. J Biol Chem 2002;277(42):39739–48. DOI: 10.1074/jbc.M200562200.</mixed-citation></ref><ref id="B18"><label>18.</label><mixed-citation>Ichimura T., Bonventre J.V., Bailly V. et al. Kidney injury molecule-1 (KIM-1), a putative epithelial cell adhesion molecule containing a novel immunoglobulin domain, is up-regulated in renal cells after injury. J Biol Chem 1998;273(7):4135–42. DOI: 10.1074/jbc.273.7.4135.</mixed-citation></ref><ref id="B19"><label>19.</label><mixed-citation>Ismail O.Z., Zhang X., Bonventre J.V., Gunaratnam L. G protein α12 (Gα12) is a negative regulator of kidney injury molecule1-mediated efferocytosis. Am J Physiol Renal Physiol 2016;310(7):607–20. DOI: 10.1152/ajprenal.00169.2015.</mixed-citation></ref><ref id="B20"><label>20.</label><mixed-citation>Medić B., Rovcanin B., Vujovic K.S. et al. Evaluation of novel biomarkers of acute kidney injury: the possibilities and limitations. Curr Med Chem 2016;23(19):1981– 97. DOI: 10.2174/092986732366616021013025.</mixed-citation></ref><ref id="B21"><label>21.</label><mixed-citation>Yin C., Wang N. Kidney injury molecule-1 in kidney disease. Ren Fail 2016;38(10):1567– 73. DOI: 10.1080/0886022X.2016.1193816.</mixed-citation></ref><ref id="B22"><label>22.</label><mixed-citation>Tami C., Silberstein E., Manangeeswaran M. et al. Immunoglobulin A (IgA) is a natural ligand of hepatitis A virus cellular receptor 1 (HAVCR-1), and the association of IgA with HAVCR-1 enhances virus-receptor interactions. J Virol 2007;81(7):3437–46. DOI: 10.1128/JVI.01585-06.</mixed-citation></ref><ref id="B23"><label>23.</label><mixed-citation>Amin R.P., Vickers A.E., Sistare F. et al. Identification of putative gene based markers of renal toxicity. Environ Health Perspect 2004;112(4):465–79. DOI: 10.1289/ehp.6683.</mixed-citation></ref><ref id="B24"><label>24.</label><mixed-citation>Lim A.I., Tang S.C., Lai K.N., Leung J.C. Kidney injury molecule-1: more than just an injury marker of tubular epithelial cells? J Cell Physiol 2013;228(5):917–24. DOI: 10.1002/jcp.24267.</mixed-citation></ref><ref id="B25"><label>25.</label><mixed-citation>Ichimura T., Brooks C.R., Bonventre J.V. Kim-1/Tim-1 and immune cells: shifting sands. Kidney Int 2012;81(9):809–11. DOI: 10.1038/ki.2012.11.</mixed-citation></ref><ref id="B26"><label>26.</label><mixed-citation>Van Timmeren M.M., van den Heuvel M.C., Bailly V. et al. Tubular kidney injury molecule1 (KIM-1) in human renal disease. J Pathol 2007;212(2):209–17. DOI: 10.1002/path.2175.</mixed-citation></ref><ref id="B27"><label>27.</label><mixed-citation>Kramer A.B., van Timmeren M.M., Schuurs T.A. et al. Reduction of proteinuria in adriamycininduced nephropathy is associated with reduction of renal kidney injury molecule (Kim-1) over time. Am J Physiol Renal Physiol 2009;296(5):1136–45. DOI: 10.1152/ajprenal.00541.2007.</mixed-citation></ref><ref id="B28"><label>28.</label><mixed-citation>Kuehn E.W., Park K.M., Somlo S., Bonventre J.V. Kidney injury molecule-1 expression in murine polycystic kidney disease. Am J Physiol Renal Physiol 2002;283(6):1326–36. DOI: 10.1152/ajprenal.00166.2002.</mixed-citation></ref><ref id="B29"><label>29.</label><mixed-citation>Ichimura T., Asseldonk E.J., Humphreys B.D. et al. Kidney injury molecule-1 is a phosphatidylserine receptor that confers a phagocytic phenotype on epithelial cells. J Clin Invest 2008;118(5):1657–68. DOI: 10.1172/JCI34487.</mixed-citation></ref><ref id="B30"><label>30.</label><mixed-citation>Silberstein E., Dveksler G., Kaplan G.G. Neutralization of hepatitis A virus (HAV) by an immunoadhesin containing the cysteinerich region of HAV cellular receptor-1. J Virol 2001;75(2):717–25. DOI: 10.1128/JVI.75.2.717-725.2001.</mixed-citation></ref><ref id="B31"><label>31.</label><mixed-citation>Rodriguez-Manzanet R., DeKruyff R., Kuchroo V.K., Umetsu D.T. The costimulatory role of TIM molecules. Immunol Rev 2009;229(1):259–70. DOI: 10.1111/j.1600-065X.2009.00772.x.</mixed-citation></ref><ref id="B32"><label>32.</label><mixed-citation>Meyers J.H., Sabatos C.A., Chakravarti S., Kuchroo V.K. The TIM gene family regulates autoimmune and allergic diseases. Trends Mol Med 2005;11(8):362–9. DOI: 10.1016/j.molmed.2005.06.008.</mixed-citation></ref><ref id="B33"><label>33.</label><mixed-citation>Gordon S. Pattern recognition receptors: doubling up for the innate immune response. Cell 2002;111(7):927–30. DOI: 10.1016/S0092-8674(02)01201-1.</mixed-citation></ref><ref id="B34"><label>34.</label><mixed-citation>Cohen H.T., Francis J., Mcgovern F.J. Renal-Cell Carcinoma. N Engl J Med 2005;353(23):2477–90. DOI: 10.1056/NEJMra043172.</mixed-citation></ref><ref id="B35"><label>35.</label><mixed-citation>Vilà M.R., Kaplan G.G., Feigelstock D. et al. Hepatitis A virus receptor blocks cell differentiation and is overexpressed in clear cell renal cell carcinoma. Kidney Int 2004;65(5):1761–73. DOI: 10.1111/j.1523-1755.2004.00601.x.</mixed-citation></ref><ref id="B36"><label>36.</label><mixed-citation>Kaplan G., Totsuka A., Thompson P. et al. Identification of a surface glycoprotein on African green monkey kidney cells as a receptor for hepatitis A virus. EMBO J 1996;15(16):4282–96. DOI: 10.1002/j.1460-2075.1996.tb00803.x.</mixed-citation></ref><ref id="B37"><label>37.</label><mixed-citation>Cuadros T., Trilla E., Sarró E. et al. HAVCR/ KIM-1 activates the IL-6/STAT-3 pathway in clear cell renal cell carcinoma and determines tumor progression and patient outcome. Cancer Res 2014;74(5):1416–28. DOI: 10.1158/0008-5472.CAN-13-1671.</mixed-citation></ref><ref id="B38"><label>38.</label><mixed-citation>Jung J.E., Lee H.G., Cho I.H. et al. STAT3 is a potential modulator of HIF-1-mediated VEGF expression in human renal carcinoma cells. FASEB J 2005;19(10):1296–8. DOI: 10.1096/fj.043099fje.</mixed-citation></ref><ref id="B39"><label>39.</label><mixed-citation>Martin T.A. The role of tight junctions in cancer metastasis. Semin Cell Dev Biol 2014;36:224–31. DOI: 10.1016/j.semcdb.2014.09.008.</mixed-citation></ref><ref id="B40"><label>40.</label><mixed-citation>Martin T.A., Harrison G.M., Mason M.D., Jiang W.G. HAVCR-1 reduces the integrity of human endothelial tight junctions. Anticancer Res 2011;31(2):467–73.</mixed-citation></ref><ref id="B41"><label>41.</label><mixed-citation>Dong Y.C., Wu B., Wang J.D. et al. Expression and clinical significance of kidney injury molecule-1 in renal epithelial neoplasms. Zhonghua Bing Li Xue Za Zhi 2010;39(1):35–9.</mixed-citation></ref><ref id="B42"><label>42.</label><mixed-citation>Mijuskovic M., Stanojevic I., Milovic N. et al. Tissue and urinary KIM-1 relate to tumor characteristics in patients with clear renal cell carcinoma. Int Urol Nephrol 2018;50(1):63–70. DOI: 10.1007/s11255017-1724-6.</mixed-citation></ref><ref id="B43"><label>43.</label><mixed-citation>Shalabi A., Abassi Z., Awad H. et al. Urinary NGAL and KIM-1: potential association with histopathologic features in patients with renal cell carcinoma. World J Urol 2013;31(6):1541–5. DOI: 10.1007/s00345013-1043-1.</mixed-citation></ref><ref id="B44"><label>44.</label><mixed-citation>Lin F., Zhang P.L., Yang X.J. et al. Human kidney injury molecule-1 (hKIM-1): a useful immunohistochemical marker for diagnosing renal cell carcinoma and ovarian clear cell carcinoma. Am J Surg Pathol 2007;31(3):371–81. DOI: 10.1097/01.pas.0000213353.95508.67.</mixed-citation></ref><ref id="B45"><label>45.</label><mixed-citation>Dent J., Hall G.D., Wilkinson N. et al. Cytogenetic alterations in ovarian clear cell carcinoma detected by comparative genomic hybridization. Br J Cancer 2003;88(10):1578–83. DOI: 10.1038/sj.bjc.6600896.</mixed-citation></ref><ref id="B46"><label>46.</label><mixed-citation>Sangoi A.R., McKenney J.K., Brooks J.D. et al. Evaluation of putative renal cell carcinoma markers PAX-2, PAX-8, and hKIM-1 in germ cell tumors: a tissue microarray study of 100 cases. Appl Immunohistochem Mol Morphol 2012;20(5):451–3. DOI: 10.1097/PAI.0b013e31824bb404.</mixed-citation></ref><ref id="B47"><label>47.</label><mixed-citation>Liu L., Song Z., Zhao Y. et al. HAVCR-1 expression might be a novel prognostic factor for gastric cancer. PLoS One 2018;13(11):0206423. DOI: 10.1371/journal.pone.0206423.</mixed-citation></ref><ref id="B48"><label>48.</label><mixed-citation>Telford E.J., Jiang W.G., Martin T.A. HAVCR-1 involvement in cancer progression. Histol Histopathol 2017;32(2):121–8. DOI: 10.14670/HH-11-817.</mixed-citation></ref><ref id="B49"><label>49.</label><mixed-citation>Wang Y., Martin T.A., Jiang W.G. HAVCR-1 expression in human colorectal cancer and its effects on colorectal cancer cells in vitro. Anticancer Res 2013;33(1):207–14.</mixed-citation></ref><ref id="B50"><label>50.</label><mixed-citation>Seibert F.S., Sitz M., Passfall J. et al. Prognostic value of urinary calprotectin, NGAL and KIM-1 in chronic kidney disease. Kidney Blood Press Res 2018;43(4):1255–62. DOI: 10.1159/000492407.</mixed-citation></ref><ref id="B51"><label>51.</label><mixed-citation>Zhao X., Zhang Y., Li L. et al. Glomerular expression of kidney injury molecule-1 and podocytopenia in diabetic glomerulopathy. Am J Nephrol 2011;34(3):268–80. DOI: 10.1159/000330187.</mixed-citation></ref><ref id="B52"><label>52.</label><mixed-citation>De Carvalho J.A., Tatsch E., Hausen B.S. et al. Urinary kidney injury molecule-1 and neutrophil gelatinase-associated lipocalin as indicators of tubular damage in normoalbuminuric patients with type 2 diabetes. Clin Biochem 2016;49(3):232–6. DOI: 10.1016/j.clinbiochem.2015.10.016.</mixed-citation></ref><ref id="B53"><label>53.</label><mixed-citation>Waikar S.S., Sabbisetti V., Ärnlöv J. et al. Relationship of proximal tubular injury to chronic kidney disease as assessed by urinary kidney injury molecule-1 in five cohort studies. Nephrol Dial Transplant 2016;31(9):1460–70. DOI: 10.1093/ndt/gfw203.</mixed-citation></ref><ref id="B54"><label>54.</label><mixed-citation>Sun I.O., Santelli A., Abumoawad A. et al. Loss of renal peritubular capillaries in hypertensive patients is detectable by urinary endothelial microparticle levels. Hypertension 2018;72(5):1180–8. DOI: 10.1161/HYPERTENSIONAHA.118.11766.</mixed-citation></ref><ref id="B55"><label>55.</label><mixed-citation>Dallatu M.K., Nwokocha E., Agu N. et al. The role of hypoxia-inducible factor/prolyl hydroxylation pathway in deoxycorticosterone acetate/salt hypertension in the rat. J Hypertens (Los Angel) 2014;3(6). DOI: 10.4172/2167-1095.1000184.</mixed-citation></ref><ref id="B56"><label>56.</label><mixed-citation>Kandhare A.D., Patil M.V., Bodhankar S.L. L-Arginine attenuates the ethylene glycol induced urolithiasis in ininephrectomized hypertensive rats: role of KIM-1, NGAL, and NOs. Ren Fail 2015;37(4):709–21. DOI: 10.3109/0886022X.2015.1011967.</mixed-citation></ref><ref id="B57"><label>57.</label><mixed-citation>Lacquaniti A., Donato V., Pintaudi B. et al. “Normoalbuminuric” diabetic nephropathy: tubular damage and NGAL. Acta Diabetol 2013;50(6):935–42. DOI: 10.1007/s00592-013-0485-7.</mixed-citation></ref><ref id="B58"><label>58.</label><mixed-citation>Humphreys B.D., Xu F., Sabbisetti V. et al. Chronic epithelial kidney injury molecule-1 expression causes murine kidney fibrosis. J Clin Invest 2013;123(9):4023–35. DOI: 10.1172/JCI45361.</mixed-citation></ref><ref id="B59"><label>59.</label><mixed-citation>Chawla L.S., Eggers P.W., Star R.A., Kimmel P.L. Acute kidney injury and chronic kidney disease as interconnected syndromes. N Engl J Med 2014;371(1):58–66. DOI: 10.1056/NEJMra1214243.</mixed-citation></ref><ref id="B60"><label>60.</label><mixed-citation>Dubin R.F., Judd S., Scherzer R. et al. Urinary tubular injury biomarkers are associated with ESRD and death in the REGARDS study. Kidney Int Rep 2018;3(5):1183–92. DOI: 10.1016/j.ekir.2018.05.013.</mixed-citation></ref><ref id="B61"><label>61.</label><citation-alternatives><mixed-citation xml:lang="en">Brovko M.Yu., Pulin A.A., Kustova T.Yu. et al. Significance of the determination of urinary excretion of kidney injury molecule-1 (KIM-1) in the assessment of the activity and prognosis of chronic glomerulonephritis. Terapevticheskiy arkhiv = Therapeutic Archive 2016;88(6):51–7. (In Russ.). DOI: 10.17116/terarkh201688651-57.</mixed-citation><mixed-citation xml:lang="ru">Бровко М.Ю., Пулин А.А., Кустова Т.Ю. и др. Значение определения экскреции с мочой молекулы повреждения почек (KIM-1) в оценке активности и прогноза течения хронического гломерулонефрита. Терапевтический архив 2016;88(6):51–7. DOI: 10.17116/terarkh201688651-57.</mixed-citation></citation-alternatives></ref><ref id="B62"><label>62.</label><mixed-citation>Lieberthal J.G., Cuthbertson D., Carette S. et al. Urinary biomarkers in relapsing antineutrophil cytoplasmic antibody-associated vasculitis. J Rheumatol 2013;40(5):674–83. DOI: 10.3899/jrheum.120879.</mixed-citation></ref><ref id="B63"><label>63.</label><mixed-citation>Xu P.C., Zhang J.J., Chen M. et al. Urinary kidney injury molecule-1 in patients with IgA nephropathy is closely associated with disease severity. Nephrol Dial Transplant 2011;26(10):3229–36. DOI: 10.1093/ndt/gfr023.</mixed-citation></ref><ref id="B64"><label>64.</label><mixed-citation>Fahmy N., Sener A., Sabbisetti V. et al. Urinary expression of novel tissue markers of kidney injury after ureteroscopy, shockwave lithotripsy, and in normal healthy controls. J Endourol 2013;27(12):1455–62. DOI: 10.1089/end.2013.0188.</mixed-citation></ref><ref id="B65"><label>65.</label><mixed-citation>Urbschat A., Gauer S., Paulus P. et al. Serum and urinary NGAL but not KIM-1 raises in human postrenal AKI. Eur J Clin Invest 2014;44(7):652–9. DOI: 10.1111/eci.12283.</mixed-citation></ref><ref id="B66"><label>66.</label><mixed-citation>Arany I., Safirstein R.L. Cisplatin nephrotoxicity. Semin Nephrol 2003;23(5):460–4.</mixed-citation></ref><ref id="B67"><label>67.</label><mixed-citation>Horie S., Oya M., Nangaku M. et al. Guidelines for treatment of renal injury during cancer chemotherapy 2016. Clin Exp Nephrol 2018;22(1):210–44. DOI: 10.1007/s10157017-1448-z.</mixed-citation></ref><ref id="B68"><label>68.</label><mixed-citation>Hostetter T.H., Olson J.L., Rennke H.G. et al. Hyperfiltration in remnant nephrons: a potentially adverse response to renal ablation. J Am Soc Nephrol 2001;12(6):1315–25. DOI: 10.1152/ajprenal.1981.241.1.F85.</mixed-citation></ref><ref id="B69"><label>69.</label><mixed-citation>Dieterle F., Sistare F., Goodsaid F. et al. Renal biomarker qualification submission: A dialog between the FDA–EMEA and predictive safety testing consortium. Nat Biotechnol 2010;28(5):455–62. DOI: 10.1038/nbt.1625.</mixed-citation></ref><ref id="B70"><label>70.</label><mixed-citation>Sahni V., Choudhury D., Ahmed Z. Chemotherapyassociated renal dysfunction. Nat Rev Nephrol 2009;5(8):450–62. DOI: 10.1038/nrneph.2009.97.</mixed-citation></ref><ref id="B71"><label>71.</label><mixed-citation>Mohamad M.A., Mohamad R.A., Fatemeh A., Mohamad R.S. Histological study of toxic effects of cisplatin single dose injection on rat kidney. Gene Cell Tissue 2014;1:21536. DOI: 10.17795/gct-21536.</mixed-citation></ref><ref id="B72"><label>72.</label><mixed-citation>Kokura K., Kuromi Y., Endo T. et al. A kidney injury molecule-1 (Kim-1) gene reporter in a mouse artificial chromosome: the responsiveness to cisplatin toxicity in immortalized mouse kidney S3 cells. J Gene Med 2016;18(10):273–81. DOI: 10.1002/jgm.2925.</mixed-citation></ref><ref id="B73"><label>73.</label><mixed-citation>Park E.J., Kwon H.K., Choi Y.M. et al. Doxorubicin induces cytotoxicity through upregulation of pERK-dependent ATF3. PLoS One 2012;7(9):44990. DOI: 10.1371/journal.pone.0044990.</mixed-citation></ref><ref id="B74"><label>74.</label><mixed-citation>Tekce B.K., Uyeturk U., Tekce H. et al. Does the kidney injury molecule-1 predict cisplatin-induced kidney injury in early stage? Ann Clin Biochem 2015;52(Pt 1):88– 94. DOI: 10.1177/0004563214528312.</mixed-citation></ref><ref id="B75"><label>75.</label><mixed-citation>Shinke H., Masuda S., Togashi Y. et al. Urinary kidney injury molecule-1 and monocyte chemotactic protein-1 are noninvasive biomarkers of cisplatin-induced nephrotoxicity in lung cancer patients. Cancer Chemother Pharmacol 2015;76(5):989–96. DOI: 10.1007/s00280-015-2880-y.</mixed-citation></ref><ref id="B76"><label>76.</label><mixed-citation>Abdelsalam M., Elmorsy E., Abdelwahab H. et al. Urinary biomarkers for early detection of platinum based drugs induced nephrotoxicity. BMC Nephrol 2018;19(1):219. DOI: 10.1186/s12882-018-1022-2.</mixed-citation></ref><ref id="B77"><label>77.</label><mixed-citation>Carvalho Pedrosa D., Macedo de Oliveira Neves F., Cavalcante Meneses G. et al. Urinary KIM-1 in children undergoing nephrotoxic antineoplastic treatment: a prospective cohort study. Pediatr Nephrol 2015;30(12):2207–13. DOI: 10.1007/s00467-015-3178-3.</mixed-citation></ref><ref id="B78"><label>78.</label><mixed-citation>Sinha V., Vence L.M., Salahudeen A.K. Urinary tubular protein-based biomarkers in the rodent model of cisplatin nephrotoxicity: a comparative analysis of serum creatinine, renal histology, and urinary KIM-1, NGAL, and NAG in the initiation, maintenance, and recovery phases of acute kidney injury. J Investig Med 2013;61(3):564–8. DOI: 10.2310/JIM.0b013e31828233a8.</mixed-citation></ref><ref id="B79"><label>79.</label><mixed-citation>Pianta T.J., Succar L., Davidson T. et al. Monitoring treatment of acute kidney injury with damage biomarkers. Toxicol Lett 2017;268:63–70. DOI: 10.1016/j.toxlet.2017.01.001.</mixed-citation></ref></ref-list></back></article>
