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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">Pediatric Hematology/Oncology and Immunopathology</journal-id><journal-title-group><journal-title xml:lang="en">Pediatric Hematology/Oncology and Immunopathology</journal-title><trans-title-group xml:lang="ru"><trans-title>Вопросы гематологии/онкологии и иммунопатологии в педиатрии</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1726-1708</issn><issn publication-format="electronic">2414-9314</issn><publisher><publisher-name xml:lang="en">Fund Doctors, Innovations, Science for Children</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">628</article-id><article-id pub-id-type="doi">10.24287/1726-1708-2022-21-2-157-166</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>LITERATURE REVIEW</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ОБЗОР ЛИТЕРАТУРЫ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">The role of gangliosides in the modulation of carcinogenesis</article-title><trans-title-group xml:lang="ru"><trans-title>Роль ганглиозидов в модуляции канцерогенеза</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-9927-8445</contrib-id><name-alternatives><name xml:lang="en"><surname>Ivanov</surname><given-names>N. S.</given-names></name><name xml:lang="ru"><surname>Иванов</surname><given-names>Н. С.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p><bold>Nikolay S. Ivanov</bold>, a pediatrician, a resident in Pediatric Oncology</p><p>1 Samory Mashela St., Moscow 117997</p></bio><bio xml:lang="ru"><p><bold>Иванов Николай Сергеевич</bold>, врач-педиатр, врач-ординатор по специальности «детская онкология»</p><p>117997, Москва, ул. Саморы Машела, 1</p></bio><email>greatinsmd@gmail.com</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-6083-6588</contrib-id><name-alternatives><name xml:lang="en"><surname>Kholodenko</surname><given-names>R. V.</given-names></name><name xml:lang="ru"><surname>Холоденко</surname><given-names>Р. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Moscow</p></bio><bio xml:lang="ru"><p>Москва</p></bio><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-3704-8783</contrib-id><name-alternatives><name xml:lang="en"><surname>Kachanov</surname><given-names>D. Yu.</given-names></name><name xml:lang="ru"><surname>Качанов</surname><given-names>Д. Ю.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Moscow</p></bio><bio xml:lang="ru"><p>Москва</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-2128-0078</contrib-id><name-alternatives><name xml:lang="en"><surname>Larin</surname><given-names>S. S.</given-names></name><name xml:lang="ru"><surname>Ларин</surname><given-names>С. С.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Moscow</p></bio><bio xml:lang="ru"><p>Москва</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-0539-6393</contrib-id><name-alternatives><name xml:lang="en"><surname>Mollaev</surname><given-names>M. D.</given-names></name><name xml:lang="ru"><surname>Моллаев</surname><given-names>М. Д.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Moscow</p></bio><bio xml:lang="ru"><p>Москва</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-3767-4477</contrib-id><name-alternatives><name xml:lang="en"><surname>Shamanskaya</surname><given-names>T. V.</given-names></name><name xml:lang="ru"><surname>Шаманская</surname><given-names>Т. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Moscow</p></bio><bio xml:lang="ru"><p>Москва</p></bio><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology of Ministry of Healthcare of the Russian Federation</institution></aff><aff><institution xml:lang="ru">ФГБУ «Национальный медицинский исследовательский центр детской гематологии, онкологии и иммунологии им. Дмитрия Рогачева» Минздрава России</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">M.M. Shemyakin and Yu.A. Ovchinnikov Institute of Bioorganic Chemistry of the Russian Academy of Sciences</institution></aff><aff><institution xml:lang="ru">ФГБУН Институт биоорганической химии им. академиков М.М. Шемякина и Ю.А. Овчинникова РАН</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2022-07-08" publication-format="electronic"><day>08</day><month>07</month><year>2022</year></pub-date><volume>21</volume><issue>2</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>157</fpage><lpage>166</lpage><history><date date-type="received" iso-8601-date="2022-06-26"><day>26</day><month>06</month><year>2022</year></date><date date-type="accepted" iso-8601-date="2022-06-26"><day>26</day><month>06</month><year>2022</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2025, «D. Rogachev NMRCPHOI»</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2025, ФГБУ «НМИЦ ДГОИ им. Дмитрия Рогачева» Минздрава России</copyright-statement><copyright-year>2025</copyright-year><copyright-holder xml:lang="en">«D. Rogachev NMRCPHOI»</copyright-holder><copyright-holder xml:lang="ru">ФГБУ «НМИЦ ДГОИ им. Дмитрия Рогачева» Минздрава России</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://hemoncim.com/jour/article/view/628">https://hemoncim.com/jour/article/view/628</self-uri><abstract xml:lang="en"><p>   Gangliosides are complex glycosphingolipids which contain ceramide and various oligosaccharides usually bearing sialic acids. An interesting feature of gangliosides is that their quantitative and qualitative composition changes during oncogenesis. This process is specific and depends on the histological type of a tumor and its functional status even within one neoplasm. On the other hand, latest advances in understanding structural and functional organization of glycosphingolipids, and primarily insights into lipid raft formation, showed that gangliosides may take part in the regulation of the activity of kinases mediating the modulation of signaling pathways involved in the malignant potential of cells. This article describes basic concepts of gangliosides and their biological role in signaling pathways involved in tumor development. We focused on experimental studies revealing both inhibitory and activating effects on important protein receptors responsible for cell proliferation, differentiation and death.</p></abstract><trans-abstract xml:lang="ru"><p>   Ганглиозиды – сложные соединения, относящиеся к классу гликосфинголипидов, несущие в своем составе церамид и различные олигосахариды, в которых обычно присутствуют сиаловые кислоты. Интересной особенностью ганглиозидов является изменение их количественного и качественного состава в процессе онкогенеза, что характеризуется определенной специфичностью в зависимости от гистологического типа опухоли и функционального статуса в пределах даже одного новообразования. С другой стороны, современные достижения в понимании структурной и функциональной организации гликосфинголипидов, в первую очередь в контексте формирования липидных рафтов, продемонстрировали возможность участия ганглиозидов в регуляции активности киназ, опосредующих модуляцию сигнальных путей, детерминирующих формирование злокачественного потенциала клеток. В статье рассмотрены фундаментальные представления о биологической роли ганглиозидов в проведении сигнальных путей, вовлеченных в регуляцию опухолевого процесса, с акцентом на экспериментальные исследования, демонстрирующие как ингибирующее, так и активирующее влияние на важные белковые рецепторы, ответственные за пролиферацию, дифференцировку и гибель клеток.</p></trans-abstract><kwd-group xml:lang="en"><kwd>gangliosides</kwd><kwd>carcinogenesis</kwd><kwd>GD2</kwd><kwd>neuroblastoma</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>ганглиозиды</kwd><kwd>канцерогенез</kwd><kwd>GD2</kwd><kwd>нейробластома</kwd></kwd-group><funding-group><funding-statement xml:lang="en">Not specified</funding-statement><funding-statement xml:lang="ru">Не указан</funding-statement></funding-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><citation-alternatives><mixed-citation xml:lang="en">1. Schnaar R. L. The Biology of Gangliosides. Adv Carbohydr Chem Biochem 2019; 76: 113–48. DOI: 10.1016/bs.accb.2018.09.002</mixed-citation><mixed-citation xml:lang="ru">Schnaar R. L. The Biology of Gangliosides. Adv Carbohydr Chem Biochem 2019; 76: 113–48. DOI: 10.1016/bs.accb.2018.09.002</mixed-citation></citation-alternatives></ref><ref id="B2"><label>2.</label><citation-alternatives><mixed-citation xml:lang="en">2. Kolter T., Sandhoff K. Sphingolipids-Their Metabolic Pathways and the Pathobiochemistry of Neurodegenerative Diseases. Angew Chem Int Ed Engl 1999; 38 (11): 1532–68. DOI: 10.1002/(SICI)1521-3773(19990601)38:11&lt;1532::AID-ANIE1532&gt;3.0.CO;2-U</mixed-citation><mixed-citation xml:lang="ru">Kolter T., Sandhoff K. Sphingolipids-Their Metabolic Pathways and the Pathobiochemistry of Neurodegenerative Diseases. Angew Chem Int Ed Engl 1999; 38 (11): 1532–68. DOI: 10.1002/(SICI)1521-3773(19990601)38:11&lt;1532::AID-ANIE1532&gt;3.0.CO;2-U</mixed-citation></citation-alternatives></ref><ref id="B3"><label>3.</label><citation-alternatives><mixed-citation xml:lang="en">3. Sandhoff R., Sandhoff K. Emerging concepts of ganglioside metabolism. FEBS Lett 2018; 592 (23): 3835–64. DOI: 10.1002/1873-3468.13114</mixed-citation><mixed-citation xml:lang="ru">Sandhoff R., Sandhoff K. Emerging concepts of ganglioside metabolism. FEBS Lett 2018; 592 (23): 3835–64. DOI: 10.1002/1873-3468.13114</mixed-citation></citation-alternatives></ref><ref id="B4"><label>4.</label><citation-alternatives><mixed-citation xml:lang="en">4. Lopez P. H., Schnaar R. L. Gangliosides in cell recognition and membrane protein regulation. Curr Opin Struct Biol 2009; 19 (5): 549–57. DOI: 10.1016/j.sbi.2009.06.001</mixed-citation><mixed-citation xml:lang="ru">Lopez P. H., Schnaar R. L. Gangliosides in cell recognition and membrane protein regulation. Curr Opin Struct Biol 2009; 19 (5): 549–57. DOI: 10.1016/j.sbi.2009.06.001</mixed-citation></citation-alternatives></ref><ref id="B5"><label>5.</label><citation-alternatives><mixed-citation xml:lang="en">5. Hakomori S. Traveling for the glycosphingolipid path. Glycoconj J 2000; 17 (7–9): 627–47. DOI: 10.1023/a:1011086929064</mixed-citation><mixed-citation xml:lang="ru">Hakomori S. Traveling for the glycosphingolipid path. Glycoconj J 2000; 17 (7–9): 627–47. DOI: 10.1023/a:1011086929064</mixed-citation></citation-alternatives></ref><ref id="B6"><label>6.</label><citation-alternatives><mixed-citation xml:lang="en">6. Sasaki N., Toyoda M., Ishiwata T. Gangliosides as Signaling Regulators in Cancer. Int J Mol Sci 2021; 22 (10): 5076. DOI: 10.3390/ijms22105076</mixed-citation><mixed-citation xml:lang="ru">Sasaki N., Toyoda M., Ishiwata T. Gangliosides as Signaling Regulators in Cancer. Int J Mol Sci 2021; 22 (10): 5076. DOI: 10.3390/ijms22105076</mixed-citation></citation-alternatives></ref><ref id="B7"><label>7.</label><citation-alternatives><mixed-citation xml:lang="en">7. Mitsuda T., Furukawa K., Fukumoto S., Miyazaki H., Urano T., Furukawa K. Overexpression of ganglioside GM1 results in the dispersion of platelet-derived growth factor receptor from glycolip idenriched microdomains and in the suppression of cell growth signals. J Biol Chem 2002; 277 (13): 11239–46. DOI: 10.1074/jbc.M107756200</mixed-citation><mixed-citation xml:lang="ru">Mitsuda T., Furukawa K., Fukumoto S., Miyazaki H., Urano T., Furukawa K. Overexpression of ganglioside GM1 results in the dispersion of platelet-derived growth factor receptor from glycolip idenriched microdomains and in the suppression of cell growth signals. J Biol Chem 2002; 277 (13): 11239–46. DOI: 10.1074/jbc.M107756200</mixed-citation></citation-alternatives></ref><ref id="B8"><label>8.</label><citation-alternatives><mixed-citation xml:lang="en">8. Nishio M., Fukumoto S., Furukawa K., Ichimura A., Miyazaki H., Kusunoki S., еt al. Overexpressed GM1 suppresses nerve growth factor (NGF) signals by modulating the intracellular localization of NGF receptors and membrane fluidity in PC12 cells. J Biol Chem 2004; 279 (32): 33368–78. DOI: 10.1074/jbc.M403816200</mixed-citation><mixed-citation xml:lang="ru">Nishio M., Fukumoto S., Furukawa K., Ichimura A., Miyazaki H., Kusunoki S., еt al. Overexpressed GM1 suppresses nerve growth factor (NGF) signals by modulating the intracellular localization of NGF receptors and membrane fluidity in PC12 cells. J Biol Chem 2004; 279 (32): 33368–78. DOI: 10.1074/jbc.M403816200</mixed-citation></citation-alternatives></ref><ref id="B9"><label>9.</label><citation-alternatives><mixed-citation xml:lang="en">9. Chiricozzi E., Pomè D.Y., Maggioni M., Di Biase E., Parravicini C., Palazzolo L., еt al. Role of the GM1 ganglioside oligosaccharide portion in the TrkA-dependent neurite sprouting in neuroblastoma cells. J Neurochem 2017; 143 (6): 645–59. DOI: 10.1111/jnc.14146</mixed-citation><mixed-citation xml:lang="ru">Chiricozzi E., Pomè D.Y., Maggioni M., Di Biase E., Parravicini C., Palazzolo L., еt al. Role of the GM1 ganglioside oligosaccharide portion in the TrkA-dependent neurite sprouting in neuroblastoma cells. J Neurochem 2017; 143 (6): 645–59. DOI: 10.1111/jnc.14146</mixed-citation></citation-alternatives></ref><ref id="B10"><label>10.</label><citation-alternatives><mixed-citation xml:lang="en">10. Chiricozzi E., Biase E. D., Maggioni M., Lunghi G., Fazzari M., Pomè D. Y., еt al. GM1 promotes TrkA-mediated neuroblastoma cell differentiation by occupying a plasma membrane domain different from TrkA. J Neurochem 2019; 149 (2): 231–41. DOI: 10.1111/jnc.14685</mixed-citation><mixed-citation xml:lang="ru">Chiricozzi E., Biase E. D., Maggioni M., Lunghi G., Fazzari M., Pomè D. Y., еt al. GM1 promotes TrkA-mediated neuroblastoma cell differentiation by occupying a plasma membrane domain different from TrkA. J Neurochem 2019; 149 (2): 231–41. DOI: 10.1111/jnc.14685</mixed-citation></citation-alternatives></ref><ref id="B11"><label>11.</label><citation-alternatives><mixed-citation xml:lang="en">11. Mallei A., Rabin S. J., Mocchetti I. Autocrine regulation of nerve growth factor expression by Trk receptors. J Neurochem 2004; 90 (5): 1085–93. DOI: 10.1111/j.1471-4159.2004.02568.x</mixed-citation><mixed-citation xml:lang="ru">Mallei A., Rabin S. J., Mocchetti I. Autocrine regulation of nerve growth factor expression by Trk receptors. J Neurochem 2004; 90 (5): 1085–93. DOI: 10.1111/j.1471-4159.2004.02568.x</mixed-citation></citation-alternatives></ref><ref id="B12"><label>12.</label><citation-alternatives><mixed-citation xml:lang="en">12. Zhuo D., Guan F. Ganglioside GM1 promotes contact inhibition of growth by regulating the localization of epidermal growth factor receptor from glycosphingolipid-enriched microdomain to caveolae. Cell Prolif 2019; 52 (4): e12639. DOI: 10.1111/cpr.12639</mixed-citation><mixed-citation xml:lang="ru">Zhuo D., Guan F. Ganglioside GM1 promotes contact inhibition of growth by regulating the localization of epidermal growth factor receptor from glycosphingolipid-enriched microdomain to caveolae. Cell Prolif 2019; 52 (4): e12639. DOI: 10.1111/cpr.12639</mixed-citation></citation-alternatives></ref><ref id="B13"><label>13.</label><citation-alternatives><mixed-citation xml:lang="en">13. Nishio M., Tajima O., Furukawa K., Urano T., Furukawa K. Over-expression of GM1 enhances cell proliferation with epidermal growth factor without affecting the receptor localization in the microdomain in PC12 cells. Int J Oncol 2005; 26 (1): 191–9.</mixed-citation><mixed-citation xml:lang="ru">Nishio M., Tajima O., Furukawa K., Urano T., Furukawa K. Over-expression of GM1 enhances cell proliferation with epidermal growth factor without affecting the receptor localization in the microdomain in PC12 cells. Int J Oncol 2005; 26 (1): 191–9.</mixed-citation></citation-alternatives></ref><ref id="B14"><label>14.</label><citation-alternatives><mixed-citation xml:lang="en">14. Todeschini A. R., Dos Santos J. N., Handa K., Hakomori S. I. Ganglioside GM2-tetraspanin CD82 complex inhibits met and its cross-talk with integrins, providing a basis for control of cell motility through glycosynapse. J Biol Chem 2007; 282 (11): 8123–33. DOI: 10.1074/jbc.M611407200</mixed-citation><mixed-citation xml:lang="ru">Todeschini A. R., Dos Santos J. N., Handa K., Hakomori S. I. Ganglioside GM2-tetraspanin CD82 complex inhibits met and its cross-talk with integrins, providing a basis for control of cell motility through glycosynapse. J Biol Chem 2007; 282 (11): 8123–33. DOI: 10.1074/jbc.M611407200</mixed-citation></citation-alternatives></ref><ref id="B15"><label>15.</label><citation-alternatives><mixed-citation xml:lang="en">15. Todeschini A. R., Dos Santos J. N., Handa K., Hakomori S. I. Ganglioside GM2/GM3 complex affixed on silica nanospheres strongly inhibits cell motility through CD82/cMet-mediated pathway. Proc Natl Acad Sci U S A 2008; 105 (6): 1925–30. DOI: 10.1073/pnas.0709619104</mixed-citation><mixed-citation xml:lang="ru">Todeschini A. R., Dos Santos J. N., Handa K., Hakomori S. I. Ganglioside GM2/GM3 complex affixed on silica nanospheres strongly inhibits cell motility through CD82/cMet-mediated pathway. Proc Natl Acad Sci U S A 2008; 105 (6): 1925–30. DOI: 10.1073/pnas.0709619104</mixed-citation></citation-alternatives></ref><ref id="B16"><label>16.</label><citation-alternatives><mixed-citation xml:lang="en">16. Chung T. W., Kim S. J., Choi H. J., Kim K. J., Kim M. J., Kim S. H., еt al. Ganglioside GM3 inhibits VEGF/VEGFR-2-mediated angiogenesis: direct interaction of GM3 with VEGFR-2. Glycobiology 2009; 19 (3): 229–39. DOI: 10.1093/glycob/cwn114</mixed-citation><mixed-citation xml:lang="ru">Chung T. W., Kim S. J., Choi H. J., Kim K. J., Kim M. J., Kim S. H., еt al. Ganglioside GM3 inhibits VEGF/VEGFR-2-mediated angiogenesis: direct interaction of GM3 with VEGFR-2. Glycobiology 2009; 19 (3): 229–39. DOI: 10.1093/glycob/cwn114</mixed-citation></citation-alternatives></ref><ref id="B17"><label>17.</label><citation-alternatives><mixed-citation xml:lang="en">17. Seyfried T. N., Mukherjee P. Ganglioside GM3 Is Antiangiogenic in Malignant Brain Cancer. J Oncol 2010; 2010: 961243. URL: https://pubmed.ncbi.nlm.nih.gov/20634908/</mixed-citation><mixed-citation xml:lang="ru">Seyfried T. N., Mukherjee P. Ganglioside GM3 Is Antiangiogenic in Malignant Brain Cancer. J Oncol 2010; 2010: 961243. URL: https://pubmed.ncbi.nlm.nih.gov/20634908/</mixed-citation></citation-alternatives></ref><ref id="B18"><label>18.</label><citation-alternatives><mixed-citation xml:lang="en">18. Meuillet E., Cremel G., Dreyfus H., Hicks D. Differential modulation of basic fibroblast and epidermal growth factor receptor activation by ganglioside GM3 in cultured retinal Müller glia. Glia 1996; 17 (3): 206–16. DOI: 10.1002/(SICI)1098-1136(199607)17:3&lt;206::AID-GLIA3&gt;3.0.CO;2-Z</mixed-citation><mixed-citation xml:lang="ru">Meuillet E., Cremel G., Dreyfus H., Hicks D. Differential modulation of basic fibroblast and epidermal growth factor receptor activation by ganglioside GM3 in cultured retinal Müller glia. Glia 1996; 17 (3): 206–16. DOI: 10.1002/(SICI)1098-1136(199607)17:3&lt;206::AID-GLIA3&gt;3.0.CO;2-Z</mixed-citation></citation-alternatives></ref><ref id="B19"><label>19.</label><citation-alternatives><mixed-citation xml:lang="en">19. Toledo M. S., Suzuki E., Handa K., Hakomori S. Cell growth regulation through GM3-enriched microdomain (glycosynapse) in human lung embryonal fibroblast WI38 and its oncogenic transformant VA13. J Biol Chem 2004; 279 (33): 34655–64. DOI: 10.1074/jbc.M403857200</mixed-citation><mixed-citation xml:lang="ru">Toledo M. S., Suzuki E., Handa K., Hakomori S. Cell growth regulation through GM3-enriched microdomain (glycosynapse) in human lung embryonal fibroblast WI38 and its oncogenic transformant VA13. J Biol Chem 2004; 279 (33): 34655–64. DOI: 10.1074/jbc.M403857200</mixed-citation></citation-alternatives></ref><ref id="B20"><label>20.</label><citation-alternatives><mixed-citation xml:lang="en">20. Prinetti A., Aureli M., Illuzzi G., Prioni S., Nocco V., Scandroglio F., еt al. GM3 synthase overexpression results in reduced cell motility and in caveolin-1 upregulation in human ovarian carcinoma cells. Glycobiology 2010; 20 (1): 62–77. DOI: 10.1093/glycob/cwp143</mixed-citation><mixed-citation xml:lang="ru">Prinetti A., Aureli M., Illuzzi G., Prioni S., Nocco V., Scandroglio F., еt al. GM3 synthase overexpression results in reduced cell motility and in caveolin-1 upregulation in human ovarian carcinoma cells. Glycobiology 2010; 20 (1): 62–77. DOI: 10.1093/glycob/cwp143</mixed-citation></citation-alternatives></ref><ref id="B21"><label>21.</label><citation-alternatives><mixed-citation xml:lang="en">21. Prinetti A., Cao T., Illuzzi G., Prioni S., Aureli M., Gagliano N., еt al. A glycosphingolipid/caveolin-1 signaling complex inhibits motility of human ovarian carcinoma cells. J Biol Chem 2011; 286 (47): 40900–10. DOI: 10.1074/jbc.M111.286146</mixed-citation><mixed-citation xml:lang="ru">Prinetti A., Cao T., Illuzzi G., Prioni S., Aureli M., Gagliano N., еt al. A glycosphingolipid/caveolin-1 signaling complex inhibits motility of human ovarian carcinoma cells. J Biol Chem 2011; 286 (47): 40900–10. DOI: 10.1074/jbc.M111.286146</mixed-citation></citation-alternatives></ref><ref id="B22"><label>22.</label><citation-alternatives><mixed-citation xml:lang="en">22. Mitsuzuka K., Handa K., Satoh M., Arai Y., Hakomori S. A specific microdomain ("glycosynapse 3") controls phenotypic conversion and reversion of bladder cancer cells through GM3-mediated interaction of alpha3beta1 integrin with CD9. J Biol Chem 2005; 280 (42): 35545–53. DOI: 10.1074/jbc.M505630200</mixed-citation><mixed-citation xml:lang="ru">Mitsuzuka K., Handa K., Satoh M., Arai Y., Hakomori S. A specific microdomain ("glycosynapse 3"); controls phenotypic conversion and reversion of bladder cancer cells through GM3-mediated interaction of alpha3beta1 integrin with CD9. J Biol Chem 2005; 280 (42): 35545–53. DOI: 10.1074/jbc.M505630200</mixed-citation></citation-alternatives></ref><ref id="B23"><label>23.</label><citation-alternatives><mixed-citation xml:lang="en">23. Hakomori S. I., Handa K. GM3 and cancer. Glycoconj J 2015; 32 (1–2): 1–8. DOI: 10.1007/s10719-014-9572-4</mixed-citation><mixed-citation xml:lang="ru">Hakomori S. I., Handa K. GM3 and cancer. Glycoconj J 2015; 32 (1–2): 1–8. DOI: 10.1007/s10719-014-9572-4</mixed-citation></citation-alternatives></ref><ref id="B24"><label>24.</label><citation-alternatives><mixed-citation xml:lang="en">24. Shibuya H., Hamamura K., Hotta H., Matsumoto Y., Nishida Y., Hattori H., еt al. Enhancement of malignant properties of human osteosarcoma cells with disialyl gangliosides GD2/GD3. Cancer Sci 2012; 103 (9): 1656–64. DOI: 10.1111/j.1349-7006.2012.02344.x</mixed-citation><mixed-citation xml:lang="ru">Shibuya H., Hamamura K., Hotta H., Matsumoto Y., Nishida Y., Hattori H., еt al. Enhancement of malignant properties of human osteosarcoma cells with disialyl gangliosides GD2/GD3. Cancer Sci 2012; 103 (9): 1656–64. DOI: 10.1111/j.1349-7006.2012.02344.x</mixed-citation></citation-alternatives></ref><ref id="B25"><label>25.</label><citation-alternatives><mixed-citation xml:lang="en">25. Cazet A., Groux-Degroote S., Teylaert B., Kwon K. M., Lehoux S., Slomianny C., еt al. GD3 synthase overexpression enhances proliferation and migration of MDA-MB-231 breast cancer cells. Biol Chem 2009; 390 (7): 601–9. DOI: 10.1515/BC.2009.054</mixed-citation><mixed-citation xml:lang="ru">Cazet A., Groux-Degroote S., Teylaert B., Kwon K. M., Lehoux S., Slomianny C., еt al. GD3 synthase overexpression enhances proliferation and migration of MDA-MB-231 breast cancer cells. Biol Chem 2009; 390 (7): 601–9. DOI: 10.1515/BC.2009.054</mixed-citation></citation-alternatives></ref><ref id="B26"><label>26.</label><citation-alternatives><mixed-citation xml:lang="en">26. Cazet A., Lefebvre J., Adriaenssens E., Julien S., Bobowski M., Grigoriadis A., еt al. GD₃ synthase expression enhances proliferation and tumor growth of MDA-MB-231 breast cancer cells through c-Met activation. Mol Cancer Res 2010; 8 (11): 1526–35. DOI: 10.1158/1541-7786.MCR-10-0302</mixed-citation><mixed-citation xml:lang="ru">Cazet A., Lefebvre J., Adriaenssens E., Julien S., Bobowski M., Grigoriadis A., еt al. GD₃ synthase expression enhances proliferation and tumor growth of MDA-MB-231 breast cancer cells through c-Met activation. Mol Cancer Res 2010; 8 (11): 1526–35. DOI: 10.1158/1541-7786.MCR-10-0302</mixed-citation></citation-alternatives></ref><ref id="B27"><label>27.</label><citation-alternatives><mixed-citation xml:lang="en">27. Cazet A., Bobowski M., Rombouts Y., Lefebvre J., Steenackers A., Popa I., еt al. The ganglioside G(D2) induces the constitutive activation of c-Met in MDA-MB-231 breast cancer cells expressing the G(D3) synthase. Glycobiology 2012; 22 (6): 806–16. DOI: 10.1093/glycob/cws049</mixed-citation><mixed-citation xml:lang="ru">Cazet A., Bobowski M., Rombouts Y., Lefebvre J., Steenackers A., Popa I., еt al. The ganglioside G(D2) induces the constitutive activation of c-Met in MDA-MB-231 breast cancer cells expressing the G(D3) synthase. Glycobiology 2012; 22 (6): 806–16. DOI: 10.1093/glycob/cws049</mixed-citation></citation-alternatives></ref><ref id="B28"><label>28.</label><citation-alternatives><mixed-citation xml:lang="en">28. Yoshida S., Fukumoto S., Kawaguchi H., Sato S., Ueda R., Furukawa K. Ganglioside G(D2) in small cell lung cancer cell lines: enhancement of cell proliferation and mediation of apoptosis. Cancer Res 2001; 61 (10): 4244–52.</mixed-citation><mixed-citation xml:lang="ru">Yoshida S., Fukumoto S., Kawaguchi H., Sato S., Ueda R., Furukawa K. Ganglioside G(D2) in small cell lung cancer cell lines: enhancement of cell proliferation and mediation of apoptosis. Cancer Res 2001; 61 (10): 4244–52.</mixed-citation></citation-alternatives></ref><ref id="B29"><label>29.</label><citation-alternatives><mixed-citation xml:lang="en">29. Вишнякова П. А. Активность каспаз в клеточной гибели, индуцированной GD2-специфичными антителами / П. А. Вишнякова [и др.] // Биоорганическая химия. – 2014. – 40 (3): 305–14.</mixed-citation><mixed-citation xml:lang="ru">Вишнякова П. А. Активность каспаз в клеточной гибели, индуцированной GD2-специфичными антителами / П. А. Вишнякова [и др.] // Биоорганическая химия. – 2014. – 40 (3): 305–14.</mixed-citation></citation-alternatives></ref><ref id="B30"><label>30.</label><citation-alternatives><mixed-citation xml:lang="en">30. Доронин И. И. Участие актиновых филаментов в реализации цитотоксического действия GD2-специфичных антител / И. И. Доронин [и др.] // Клеточные технологии в биологии и медицине. – 2018. – 4: 220–31.</mixed-citation><mixed-citation xml:lang="ru">Доронин И. И. Участие актиновых филаментов в реализации цитотоксического действия GD2-специфичных антител / И. И. Доронин [и др.] // Клеточные технологии в биологии и медицине. – 2018. – 4: 220–31.</mixed-citation></citation-alternatives></ref><ref id="B31"><label>31.</label><citation-alternatives><mixed-citation xml:lang="en">31. Battula V. L., Shi Y., Evans K. W., Wang R. Y., Spaeth E. L., Jacamo R. O., еt al. Ganglioside GD2 identifies breast cancer stem cells and promotes tumorigenesis. J Clin Invest 2012; 122 (6): 2066–78. DOI: 10.1172/JCI59735</mixed-citation><mixed-citation xml:lang="ru">Battula V. L., Shi Y., Evans K. W., Wang R. Y., Spaeth E. L., Jacamo R. O., еt al. Ganglioside GD2 identifies breast cancer stem cells and promotes tumorigenesis. J Clin Invest 2012; 122 (6): 2066–78. DOI: 10.1172/JCI59735</mixed-citation></citation-alternatives></ref><ref id="B32"><label>32.</label><citation-alternatives><mixed-citation xml:lang="en">32. Sarkar T. R., Battula V. L., Werden S. J., Vijay G. V., Ramirez-Peña E. Q., Taube J. H., еt al. GD3 synthase regulates epithelial-mesenchymal transition and metastasis in breast cancer. Oncogene 2015; 34 (23): 2958–67. DOI: 10.1038/onc.2014.245</mixed-citation><mixed-citation xml:lang="ru">Sarkar T. R., Battula V. L., Werden S. J., Vijay G. V., Ramirez-Peña E. Q., Taube J. H., еt al. GD3 synthase regulates epithelial-mesenchymal transition and metastasis in breast cancer. Oncogene 2015; 34 (23): 2958–67. DOI: 10.1038/onc.2014.245</mixed-citation></citation-alternatives></ref><ref id="B33"><label>33.</label><citation-alternatives><mixed-citation xml:lang="en">33. Иванов Н. С. Роль GD2 как диагностического и прогностического опухолевого маркера при нейробластоме (обзор литературы) / Н. С. Иванов [и др.] // Российский журнал детской гематологии и онкологии. – 2021; 8 (4): 47–59. DOI: 10.21682/2311-1267-2021-8-4-47-59</mixed-citation><mixed-citation xml:lang="ru">Иванов Н. С. Роль GD2 как диагностического и прогностического опухолевого маркера при нейробластоме (обзор литературы) / Н. С. Иванов [и др.] // Российский журнал детской гематологии и онкологии. – 2021; 8 (4): 47–59. DOI: 10.21682/2311-1267-2021-8-4-47-59</mixed-citation></citation-alternatives></ref><ref id="B34"><label>34.</label><citation-alternatives><mixed-citation xml:lang="en">34. Liu Y., Li R., Ladisch S. Exogenous ganglioside GD1a enhances epidermal growth factor receptor binding and dimerization. J Biol Chem 2004; 279 (35): 36481–9. DOI: 10.1074/jbc.M402880200</mixed-citation><mixed-citation xml:lang="ru">Liu Y., Li R., Ladisch S. Exogenous ganglioside GD1a enhances epidermal growth factor receptor binding and dimerization. J Biol Chem 2004; 279 (35): 36481–9. DOI: 10.1074/jbc.M402880200</mixed-citation></citation-alternatives></ref><ref id="B35"><label>35.</label><citation-alternatives><mixed-citation xml:lang="en">35. Yang H. J., Jung K. Y., Kwak D. H., Lee S. H., Ryu J. S., Kim J. S., еt al. Inhibition of ganglioside GD1a synthesis suppresses the differentiation of human mesenchymal stem cells into osteoblasts. Dev Growth Differ 2011; 53 (3): 323–32. DOI: 10.1111/j.1440-169X.2010.01240.x</mixed-citation><mixed-citation xml:lang="ru">Yang H. J., Jung K. Y., Kwak D. H., Lee S. H., Ryu J. S., Kim J. S., еt al. Inhibition of ganglioside GD1a synthesis suppresses the differentiation of human mesenchymal stem cells into osteoblasts. Dev Growth Differ 2011; 53 (3): 323–32. DOI: 10.1111/j.1440-169X.2010.01240.x</mixed-citation></citation-alternatives></ref><ref id="B36"><label>36.</label><citation-alternatives><mixed-citation xml:lang="en">36. Fukumoto S., Mutoh T., Hasegawa T., Miyazaki H., Okada M., Goto G., еt al. GD3 synthase gene expression in PC12 cells results in the continuous activation of TrkA and ERK1/2 and enhanced proliferation. J Biol Chem 2000; 275 (8): 5832–8. DOI: 10.1074/jbc.275.8.5832</mixed-citation><mixed-citation xml:lang="ru">Fukumoto S., Mutoh T., Hasegawa T., Miyazaki H., Okada M., Goto G., еt al. GD3 synthase gene expression in PC12 cells results in the continuous activation of TrkA and ERK1/2 and enhanced proliferation. J Biol Chem 2000; 275 (8): 5832–8. DOI: 10.1074/jbc.275.8.5832</mixed-citation></citation-alternatives></ref><ref id="B37"><label>37.</label><citation-alternatives><mixed-citation xml:lang="en">37. Mirkin B. L., Clark S. H., Zhang C. Inhibition of human neuroblastoma cell proliferation and EGF receptor phosphorylation by gangliosides GM1, GM3, GD1A and GT1B. Cell Prolif 2002; 35 (2): 105–15. DOI: 10.1046/j.1365-2184.2002.00228.x</mixed-citation><mixed-citation xml:lang="ru">Mirkin B. L., Clark S. H., Zhang C. Inhibition of human neuroblastoma cell proliferation and EGF receptor phosphorylation by gangliosides GM1, GM3, GD1A and GT1B. Cell Prolif 2002; 35 (2): 105–15. DOI: 10.1046/j.1365-2184.2002.00228.x</mixed-citation></citation-alternatives></ref><ref id="B38"><label>38.</label><citation-alternatives><mixed-citation xml:lang="en">38. Kume M., Kiyohara E., Matsumura Y., Koguchi-Yoshioka H., Tanemura A., Hanaoka Y., еt al. Ganglioside GD3 May Suppress the Functional Activities of Benign Skin T Cells in Cutaneous T-Cell Lymphoma. Front Immunol 2021; 12: 651048. DOI: 10.3389/fimmu.2021.651048</mixed-citation><mixed-citation xml:lang="ru">Kume M., Kiyohara E., Matsumura Y., Koguchi-Yoshioka H., Tanemura A., Hanaoka Y., еt al. Ganglioside GD3 May Suppress the Functional Activities of Benign Skin T Cells in Cutaneous T-Cell Lymphoma. Front Immunol 2021; 12: 651048. DOI: 10.3389/fimmu.2021.651048</mixed-citation></citation-alternatives></ref><ref id="B39"><label>39.</label><citation-alternatives><mixed-citation xml:lang="en">39. Zeng G., Gao L., Birklé S., Yu R. K. Suppression of ganglioside GD3 expression in a rat F-11 tumor cell line reduces tumor growth, angiogenesis, and vascular endothelial growth factor production. Cancer Res 2000; 60 (23): 6670–6.</mixed-citation><mixed-citation xml:lang="ru">Zeng G., Gao L., Birklé S., Yu R. K. Suppression of ganglioside GD3 expression in a rat F-11 tumor cell line reduces tumor growth, angiogenesis, and vascular endothelial growth factor production. Cancer Res 2000; 60 (23): 6670–6.</mixed-citation></citation-alternatives></ref><ref id="B40"><label>40.</label><citation-alternatives><mixed-citation xml:lang="en">40. Ohkawa Y., Momota H., Kato A., Hashimoto N., Tsuda Y., Kotani N., еt al. Ganglioside GD3 Enhances Invasiveness of Gliomas by Forming a Complex with Platelet-de-rived Growth Factor Receptor α and Yes Kinase. J Biol Chem 2015; 290 (26): 16043–58. DOI: 10.1074/jbc.M114.635755</mixed-citation><mixed-citation xml:lang="ru">Ohkawa Y., Momota H., Kato A., Hashimoto N., Tsuda Y., Kotani N., еt al. Ganglioside GD3 Enhances Invasiveness of Gliomas by Forming a Complex with Platelet-de-rived Growth Factor Receptor α and Yes Kinase. J Biol Chem 2015; 290 (26): 16043–58. DOI: 10.1074/jbc.M114.635755</mixed-citation></citation-alternatives></ref><ref id="B41"><label>41.</label><citation-alternatives><mixed-citation xml:lang="en">41. Wang J., Yu R. K. Interaction of ganglioside GD3 with an EGF receptor sustains the self-renewal ability of mouse neural stem cells in vitro. Proc Natl Acad Sci U S A 2013; 110 (47): 19137–42. DOI: 10.1073/pnas.1307224110</mixed-citation><mixed-citation xml:lang="ru">Wang J., Yu R. K. Interaction of ganglioside GD3 with an EGF receptor sustains the self-renewal ability of mouse neural stem cells in vitro. Proc Natl Acad Sci U S A 2013; 110 (47): 19137–42. DOI: 10.1073/pnas.1307224110</mixed-citation></citation-alternatives></ref><ref id="B42"><label>42.</label><citation-alternatives><mixed-citation xml:lang="en">42. Furukawa K., Ohkawa Y., Yamauchi Y., Hamamura K., Ohmi Y., Furukawa K. Fine tuning of cell signals by glycosylation. J Biochem 2012; 151 (6): 573–8. DOI: 10.1093/jb/mvs043</mixed-citation><mixed-citation xml:lang="ru">Furukawa K., Ohkawa Y., Yamauchi Y., Hamamura K., Ohmi Y., Furukawa K. Fine tuning of cell signals by glycosylation. J Biochem 2012; 151 (6): 573–8. DOI: 10.1093/jb/mvs043</mixed-citation></citation-alternatives></ref><ref id="B43"><label>43.</label><citation-alternatives><mixed-citation xml:lang="en">43. Hamamura K., Furukawa K., Hayashi T., Hattori T., Nakano J., Nakashima H., еt al. Ganglioside GD3 promotes cell growth and invasion through p130Cas and paxillin in malignant melanoma cells. Proc Natl Acad Sci U S A 2005; 102 (31): 11041–6. DOI: 10.1073/pnas.0503658102</mixed-citation><mixed-citation xml:lang="ru">Hamamura K., Furukawa K., Hayashi T., Hattori T., Nakano J., Nakashima H., еt al. Ganglioside GD3 promotes cell growth and invasion through p130Cas and paxillin in malignant melanoma cells. Proc Natl Acad Sci U S A 2005; 102 (31): 11041–6. DOI: 10.1073/pnas.0503658102</mixed-citation></citation-alternatives></ref><ref id="B44"><label>44.</label><citation-alternatives><mixed-citation xml:lang="en">44. Ohkawa Y., Miyazaki S., Hamamura K., Kambe M., Miyata M., Tajima O., еt al. Ganglioside GD3 enhances adhesion signals and augments malignant properties of melanoma cells by recruiting integrins to glycolipid-enriched microdomains. J Biol Chem 2010; 285 (35): 27213–23. DOI: 10.1074/jbc.M109.087791</mixed-citation><mixed-citation xml:lang="ru">Ohkawa Y., Miyazaki S., Hamamura K., Kambe M., Miyata M., Tajima O., еt al. Ganglioside GD3 enhances adhesion signals and augments malignant properties of melanoma cells by recruiting integrins to glycolipid-enriched microdomains. J Biol Chem 2010; 285 (35): 27213–23. DOI: 10.1074/jbc.M109.087791</mixed-citation></citation-alternatives></ref><ref id="B45"><label>45.</label><citation-alternatives><mixed-citation xml:lang="en">45. Ohkawa Y., Miyazaki S., Miyata M., Hamamura K., Furukawa K., Furukawa K. Essential roles of integrin-mediated signaling for the enhancement of malignant properties of melanomas based on the expression of GD3. Biochem Biophys Res Commun 2008; 373 (1): 14–9. DOI: 10.1016/j.bbrc.2008.05.149</mixed-citation><mixed-citation xml:lang="ru">Ohkawa Y., Miyazaki S., Miyata M., Hamamura K., Furukawa K., Furukawa K. Essential roles of integrin-mediated signaling for the enhancement of malignant properties of melanomas based on the expression of GD3. Biochem Biophys Res Commun 2008; 373 (1): 14–9. DOI: 10.1016/j.bbrc.2008.05.149</mixed-citation></citation-alternatives></ref><ref id="B46"><label>46.</label><citation-alternatives><mixed-citation xml:lang="en">46. Hamamura K., Tsuji M., Hotta H., Ohkawa Y., Takahashi M., Shibuya H., еt al. Functional activation of Src family kinase yes protein is essential for the enhanced malignant properties of human melanoma cells expressing ganglioside GD3. J Biol Chem 2011; 286 (21): 18526–37. DOI: 10.1074/jbc.M110.164798</mixed-citation><mixed-citation xml:lang="ru">Hamamura K., Tsuji M., Hotta H., Ohkawa Y., Takahashi M., Shibuya H., еt al. Functional activation of Src family kinase yes protein is essential for the enhanced malignant properties of human melanoma cells expressing ganglioside GD3. J Biol Chem 2011; 286 (21): 18526–37. DOI: 10.1074/jbc.M110.164798</mixed-citation></citation-alternatives></ref><ref id="B47"><label>47.</label><citation-alternatives><mixed-citation xml:lang="en">47. Shibuya H., Hamamura K., Hotta H., Matsumoto Y., Nishida Y., Hattori H., еt al. Enhancement of malignant properties of human osteosarcoma cells with disialyl gangliosides GD2/GD3. Cancer Sci 2012; 103 (9): 1656–64. DOI: 10.1111/j.1349-7006.2012.02344.x</mixed-citation><mixed-citation xml:lang="ru">Shibuya H., Hamamura K., Hotta H., Matsumoto Y., Nishida Y., Hattori H., еt al. Enhancement of malignant properties of human osteosarcoma cells with disialyl gangliosides GD2/GD3. Cancer Sci 2012; 103 (9): 1656–64. DOI: 10.1111/j.1349-7006.2012.02344.x</mixed-citation></citation-alternatives></ref><ref id="B48"><label>48.</label><citation-alternatives><mixed-citation xml:lang="en">48. Dong L., Liu Y., Colberg-Poley A. M., Kaucic K., Ladisch S. Induction of GM1a/GD1b synthase triggers complex ganglioside expression and alters neuroblastoma cell behavior; a new tumor cell model of ganglioside function. Glycoconj J 2011; 28 (3–4): 137–47. DOI: 10.1007/s10719-011-9330-9</mixed-citation><mixed-citation xml:lang="ru">Dong L., Liu Y., Colberg-Poley A. M., Kaucic K., Ladisch S. Induction of GM1a/GD1b synthase triggers complex ganglioside expression and alters neuroblastoma cell behavior; a new tumor cell model of ganglioside function. Glycoconj J 2011; 28 (3–4): 137–47. DOI: 10.1007/s10719-011-9330-9</mixed-citation></citation-alternatives></ref><ref id="B49"><label>49.</label><citation-alternatives><mixed-citation xml:lang="en">49. Hettmer S., Malott C., Woods W., Ladisch S., Kaucic K. Biological stratification of human neuroblastoma by complex "B" pathway ganglioside expression. Cancer Res 2003; 63 (21): 7270–6.</mixed-citation><mixed-citation xml:lang="ru">Hettmer S., Malott C., Woods W., Ladisch S., Kaucic K. Biological stratification of human neuroblastoma by complex "B" pathway ganglioside expression. Cancer Res 2003; 63 (21): 7270–6.</mixed-citation></citation-alternatives></ref><ref id="B50"><label>50.</label><citation-alternatives><mixed-citation xml:lang="en">50. Wu Z. L., Schwartz E., Seeger R., Ladisch S. Expression of GD2 ganglioside by untreated primary human neuroblastomas. Cancer Res 1986; 46 (1): 440–3.</mixed-citation><mixed-citation xml:lang="ru">Wu Z. L., Schwartz E., Seeger R., Ladisch S. Expression of GD2 ganglioside by untreated primary human neuroblastomas. Cancer Res 1986; 46 (1): 440–3.</mixed-citation></citation-alternatives></ref><ref id="B51"><label>51.</label><citation-alternatives><mixed-citation xml:lang="en">51. Cheung N. K., Lazarus H., Miraldi F. D., Abramowsky C. R., Kallick S., Saarinen U.M., еt al. Ganglioside GD2 specific monoclonal antibody 3F8: a phase I study in patients with neuroblastoma and malignant melanoma. J Clin Oncol 1987; 5 (9): 1430–40. DOI: 10.1200/JCO.1987.5.9.1430</mixed-citation><mixed-citation xml:lang="ru">Cheung N. K., Lazarus H., Miraldi F. D., Abramowsky C. R., Kallick S., Saarinen U.M., еt al. Ganglioside GD2 specific monoclonal antibody 3F8: a phase I study in patients with neuroblastoma and malignant melanoma. J Clin Oncol 1987; 5 (9): 1430–40. DOI: 10.1200/JCO.1987.5.9.1430</mixed-citation></citation-alternatives></ref><ref id="B52"><label>52.</label><citation-alternatives><mixed-citation xml:lang="en">52. Yu A. L., Gilman A. L., Ozkaynak M. F., London W. B., Kreissman S. G., Chen H. X., еt al. Anti-GD2 antibody with GM-CSF, interleukin-2, and isotretinoin for neuroblastoma. N Engl J Med 2010; 363 (14): 1324–34. DOI: 10.1056/NEJMoa0911123</mixed-citation><mixed-citation xml:lang="ru">Yu A. L., Gilman A. L., Ozkaynak M. F., London W. B., Kreissman S. G., Chen H. X., еt al. Anti-GD2 antibody with GM-CSF, interleukin-2, and isotretinoin for neuroblastoma. N Engl J Med 2010; 363 (14): 1324–34. DOI: 10.1056/NEJMoa0911123</mixed-citation></citation-alternatives></ref><ref id="B53"><label>53.</label><citation-alternatives><mixed-citation xml:lang="en">53. Ladenstein R., Pötschger U., Valteau-Couanet D., Luksch R., Castel V., Ash S., еt al. Investigation of the Role of Dinutuximab Beta-Based Immunotherapy in the SIOPEN High-Risk Neuroblastoma 1 Trial (HR-NBL1). Cancers (Basel) 2020; 12 (2): 309. DOI: 10.3390/cancers12020309</mixed-citation><mixed-citation xml:lang="ru">Ladenstein R., Pötschger U., Valteau-Couanet D., Luksch R., Castel V., Ash S., еt al. Investigation of the Role of Dinutuximab Beta-Based Immunotherapy in the SIOPEN High-Risk Neuroblastoma 1 Trial (HR-NBL1). Cancers (Basel) 2020; 12 (2): 309. DOI: 10.3390/cancers12020309</mixed-citation></citation-alternatives></ref><ref id="B54"><label>54.</label><citation-alternatives><mixed-citation xml:lang="en">54. Cheung N. K., Cheung I. Y., Kushner B. H., Ostrovnaya I., Chamberlain E., Kramer K., еt al. Murine anti-GD2 monoclonal antibody 3F8 combined with granulocyte-macrophage colony-stimulating factor and 13-cis-retinoic acid in high-risk patients with stage 4 neuroblastoma in first remission. J Clin Oncol 2012; 30 (26): 3264–70. DOI: 10.1200/JCO.2011.41.3807</mixed-citation><mixed-citation xml:lang="ru">Cheung N. K., Cheung I. Y., Kushner B. H., Ostrovnaya I., Chamberlain E., Kramer K., еt al. Murine anti-GD2 monoclonal antibody 3F8 combined with granulocyte-macrophage colony-stimulating factor and 13-cis-retinoic acid in high-risk patients with stage 4 neuroblastoma in first remission. J Clin Oncol 2012; 30 (26): 3264–70. DOI: 10.1200/JCO.2011.41.3807</mixed-citation></citation-alternatives></ref><ref id="B55"><label>55.</label><citation-alternatives><mixed-citation xml:lang="en">55. Kholodenko I. V., Kalinovsky D. V., Doronin I. I., Deyev S. M., Kholodenko R. V. Neuroblastoma Origin and Therapeutic Targets for Immunotherapy. J Immunol Res 2018; 2018: 7394268. DOI: 10.1155/2018/7394268</mixed-citation><mixed-citation xml:lang="ru">Kholodenko I. V., Kalinovsky D. V., Doronin I. I., Deyev S. M., Kholodenko R. V. Neuroblastoma Origin and Therapeutic Targets for Immunotherapy. J Immunol Res 2018; 2018: 7394268. DOI: 10.1155/2018/7394268</mixed-citation></citation-alternatives></ref><ref id="B56"><label>56.</label><citation-alternatives><mixed-citation xml:lang="en">56. Sait S., Modak S. Anti-GD2 immunotherapy for neuroblastoma. Expert Rev Anticancer Ther 2017; 17 (10): 889–904. DOI: 10.1080/14737140.2017.1364995</mixed-citation><mixed-citation xml:lang="ru">Sait S., Modak S. Anti-GD2 immunotherapy for neuroblastoma. Expert Rev Anticancer Ther 2017; 17 (10): 889–904. DOI: 10.1080/14737140.2017.1364995</mixed-citation></citation-alternatives></ref><ref id="B57"><label>57.</label><citation-alternatives><mixed-citation xml:lang="en">57. Terzic T., Cordeau M., Herblot S., Teira P., Cournoyer S., Beaunoyer M., еt al. Expression of Disialoganglioside (GD2) in Neuroblastic Tumors: A Prognostic Value for Patients Treated With Anti-GD2 Immunotherapy. Pediatr Dev Pathol 2018; 21 (4): 355–62. DOI: 10.1177/1093526617723972</mixed-citation><mixed-citation xml:lang="ru">Terzic T., Cordeau M., Herblot S., Teira P., Cournoyer S., Beaunoyer M., еt al. Expression of Disialoganglioside (GD2) in Neuroblastic Tumors: A Prognostic Value for Patients Treated With Anti-GD2 Immunotherapy. Pediatr Dev Pathol 2018; 21 (4): 355–62. DOI: 10.1177/1093526617723972</mixed-citation></citation-alternatives></ref><ref id="B58"><label>58.</label><citation-alternatives><mixed-citation xml:lang="en">58. Brodeur G. M. Spontaneous regression of neuroblastoma. Cell Tissue Res 2018; 372 (2): 277–86. DOI: 10.1007/s00441-017-2761-2</mixed-citation><mixed-citation xml:lang="ru">Brodeur G. M. Spontaneous regression of neuroblastoma. Cell Tissue Res 2018; 372 (2): 277–86. DOI: 10.1007/s00441-017-2761-2</mixed-citation></citation-alternatives></ref></ref-list></back></article>
