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<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="other" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Advances in Molecular Oncology</journal-id><journal-title-group><journal-title xml:lang="en">Advances in Molecular Oncology</journal-title><trans-title-group xml:lang="ru"><trans-title>Успехи молекулярной онкологии</trans-title></trans-title-group></journal-title-group><issn publication-format="print">2313-805X</issn><issn publication-format="electronic">2413-3787</issn><publisher><publisher-name xml:lang="en">Publishing House ABV Press</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">754</article-id><article-id pub-id-type="doi">10.17650/2313-805X-2025-12-1-14-30</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>REVIEW ARTICLES</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ОБЗОРНЫЕ СТАТЬИ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">The balance between deception and adaptation: vasculogenic mimicry as a tumor survival strategy</article-title><trans-title-group xml:lang="ru"><trans-title>Баланс между обманом и адаптацией: васкулогенная мимикрия как стратегия выживания опухоли</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-1235-3829</contrib-id><name-alternatives><name xml:lang="en"><surname>Prosekina</surname><given-names>E. A.</given-names></name><name xml:lang="ru"><surname>Просекина</surname><given-names>Е. А.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Elizaveta Andreevna Prosekina </p><p>68 Leningradskaya St., Pesochny Settlement, Saint Petersburg 197758, Russia </p></bio><bio xml:lang="ru"><p>Елизавета Андреевна Просекина <bold> </bold></p><p>Россия, 197758 Санкт-Петербург, пос. Песочный, ул.  Ленинградская, 68 </p></bio><email>elizaveta.prosekina@gmail.com</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-1843-2808</contrib-id><name-alternatives><name xml:lang="en"><surname>Shapkina</surname><given-names>V. A.</given-names></name><name xml:lang="ru"><surname>Шапкина</surname><given-names>В. А.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>7/9 Universitetskaya Emb., Saint Petersburg 199034, Russia </p></bio><bio xml:lang="ru"><p>Россия, 199034 Санкт-Петербург, Университетская наб., 7/9 </p></bio><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-3913-9619</contrib-id><name-alternatives><name xml:lang="en"><surname>Karpov</surname><given-names>A. E.</given-names></name><name xml:lang="ru"><surname>Карпов</surname><given-names>А. Е.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>68 Leningradskaya St., Pesochny Settlement, Saint Petersburg 197758, Russia </p></bio><bio xml:lang="ru"><p>Россия, 197758 Санкт-Петербург, пос. Песочный, ул.  Ленинградская, 68 </p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0009-0001-3577-8379</contrib-id><name-alternatives><name xml:lang="en"><surname>Fedorutseva</surname><given-names>E. Yu.</given-names></name><name xml:lang="ru"><surname>Федоруцева</surname><given-names>Е. Ю.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>36 Lenin Prospekt, Tomsk 634050, Russia </p></bio><bio xml:lang="ru"><p>Россия, 634050 Томск, пр-кт Ленина, 36 </p></bio><xref ref-type="aff" rid="aff3"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-2948-397X</contrib-id><name-alternatives><name xml:lang="en"><surname>Artemyeva</surname><given-names>A. S.</given-names></name><name xml:lang="ru"><surname>Артемьева</surname><given-names>А. С.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>68 Leningradskaya St., Pesochny Settlement, Saint Petersburg 197758, Russia </p></bio><bio xml:lang="ru"><p>Россия, 197758 Санкт-Петербург, пос. Песочный, ул.  Ленинградская, 68 </p></bio><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">N.N. Petrov National Medical Research Center of Oncology, Ministry of Health of Russia</institution></aff><aff><institution xml:lang="ru">ФГБУ «Национальный медицинский исследовательский центр онкологии им. Н.Н. Петрова» Минздрава России</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">Saint Petersburg State University</institution></aff><aff><institution xml:lang="ru">ФГБОУ ВО «Санкт-Петербургский государственный университет»</institution></aff></aff-alternatives><aff-alternatives id="aff3"><aff><institution xml:lang="en">National Research Tomsk State University</institution></aff><aff><institution xml:lang="ru">ФГАОУ ВО «Национальный исследовательский Томский государственный университет»</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2025-01-15" publication-format="electronic"><day>15</day><month>01</month><year>2025</year></pub-date><volume>12</volume><issue>1</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>14</fpage><lpage>30</lpage><history><date date-type="received" iso-8601-date="2025-04-14"><day>14</day><month>04</month><year>2025</year></date><date date-type="accepted" iso-8601-date="2025-04-14"><day>14</day><month>04</month><year>2025</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2025, Prosekina E.A., Shapkina V.A., Karpov A.E., Fedorutseva E.Y., Artemyeva A.S.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2025, Просекина Е.А., Шапкина В.А., Карпов А.Е., Федоруцева Е.Ю., Артемьева А.С.</copyright-statement><copyright-year>2025</copyright-year><copyright-holder xml:lang="en">Prosekina E.A., Shapkina V.A., Karpov A.E., Fedorutseva E.Y., Artemyeva A.S.</copyright-holder><copyright-holder xml:lang="ru">Просекина Е.А., Шапкина В.А., Карпов А.Е., Федоруцева Е.Ю., Артемьева А.С.</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://umo.abvpress.ru/jour/article/view/754">https://umo.abvpress.ru/jour/article/view/754</self-uri><abstract xml:lang="en"><p>Vasculogenic mimicry is a unique process through which tumor cells imitate normal vascular endothelial cells to secure access to the blood flow. In this review, we consider molecular mechanisms underlying this phenomenon and its importance in the context of solid tumor development. We have analyzed survival strategies of tumor cells using vasculogenic mimicry and described potential therapeutic approaches aimed at tumor growth and metastasis suppression. Highlighting the methods of histological and molecular identification of vasculogenic mimicry promotes better understanding of this phenomenon and its early diagnosis. The review focuses on the necessity of further research in the area of vasculogenic mimicry to conceptualize mechanisms underlying carcinogenesis. We have analyzed 109 articles from the leading biomedical databases including SciVerse Scopus, PubMed, Web of Science and RSCI (Russian Science Citation Index) which allowed us to summarize current scientific data and identify the key trends in the area of molecular oncology.</p></abstract><trans-abstract xml:lang="ru"><p>Васкулогенная мимикрия представляет собой уникальный процесс, при котором опухолевые клетки имитируют нормальные эндотелиальные клетки сосудов с целью обеспечения себе доступа к кровоснабжению. В настоящем обзоре рассмотрены молекулярные механизмы, предшествующие этому явлению, а также его важность в контексте развития солидных опухолей. Мы проанализировали стратегии выживания опухолевых клеток, использующих васкулогенную мимикрию, и описали потенциальные терапевтические подходы, направленные на подавление роста и метастазирования опухоли. Освещение методов гистологической и молекулярной идентификации васкулогенной мимикрии способствует лучшему пониманию данного феномена и его ранней диагностике. В обзоре акцентируется внимание на необходимости дальнейших исследований васкулогенной мимикрии для формирования представлений о механизмах, лежащих в основе канцерогенеза. Мы проанализировали результаты 109 работ, представленных в ведущих биомедицинских базах данных, включая SciVerse Scopus, PubMed, Web of Science и РИНЦ (Российский индекс научного цитирования), что позволило обобщить актуальные научные данные и выявить ключевые тенденции в области молекулярной онкологии.</p></trans-abstract><kwd-group xml:lang="en"><kwd>vasculogenic mimicry</kwd><kwd>аngiogenesis</kwd><kwd>carcinogenesis</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>васкулогенная мимикрия</kwd><kwd>ангиогенез</kwd><kwd>канцерогенез</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Kuczynski E.A., Vermeulen P.B., Pezzella F. et al. Vessel co-option in cancer. Nat Rev Clin Oncol 2019;16(8):469–93. DOI: 10.1038/s41571-019-0181-9</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Jiang X., Wang J., Deng X. et al. The role of microenvironment in tumor angiogenesis. J Exp Clin Cancer Res 2020;39(1):1–19. DOI: 10.1186/s13046-020-01709-5</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Pinto M.P., Sotomayor P., Carrasco-Avino G. et al. Escaping antiangiogenic therapy: strategies employed by cancer cells. Int J Mol Sci 2016;17(9):1–20. DOI: 10.3390/ijms17091489</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>Maniotis A.J., Folberg R., Hess A. et al. Vascular channel formation by human melanoma cells in vivo and in vitro: vasculogenic mimicry. Am J Pathol 1999;155(3):739–52. DOI: 10.1016/S0002-9440(10)65173-5</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>Damsky C.H., Fisher S.J. Trophoblast pseudo-vasculogenesis: faking it with endothelial adhesion receptors. Curr Opin Cell Biol 1998;10(5):660–6. DOI: 10.1016/S0955-0674(98)80043-4</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>Kučera T., Strilić B., Regener K. et al. Ancestral vascular lumen formation via basal cell surfaces. PLoS One 2009;4(1):e4132. DOI: 10.1371/JOURNAL.PONE.0004132</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>Racordon D., Valdivia A., Mingo G. et al. Structural and functional identification of vasculogenic mimicry in vitro. Sci Rep 2017;7(1):1–12. DOI: 10.1038/s41598-017-07622-w</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>Paulis Y.W.J., Soetekouw P.M.М.B., Verheul H.M.W. et al. Signalling pathways in vasculogenic mimicry. Biochim Bioph Acta 2010;1806(1):18–28. DOI: 10.1016/J.BBCAN.2010.01.001</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>El Hallani S., Boisselier B., Peglion F. et al. A new alternative mechanism in glioblastoma vascularization: tubular vasculogenic mimicry. Brain 2010;133(Pt 4):973. DOI: 10.1093/BRAIN/AWQ044</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>Wang W., Lin P., Han C. et al. Vasculogenic mimicry contributes to lymph node metastasis of laryngeal squamous cell carcinoma. J Exp Clin Cancer Res 2010;29(1):60. DOI: 10.1186/1756-9966-29-60/TABLES/4</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>Ricci-Vitiani L., Lombardi D.G., Pilozzi E. et al. Identification and expansion of human colon-cancer-initiating cells. Nature 2006;445(7123):111–5. DOI: 10.1038/nature05384</mixed-citation></ref><ref id="B12"><label>12.</label><mixed-citation>Ponti D., Costa A., Zaffaroni N. et al. Isolation and in vitro propagation of tumorigenic breast cancer cells with stem/progenitor cell properties. Cancer Res 2005;65(13):5506–11. DOI: 10.1158/0008-5472.CAN-05-0626</mixed-citation></ref><ref id="B13"><label>13.</label><mixed-citation>Liu Z., Li Y., Zhao W. et al. Demonstration of vasculogenic mimicry in astrocytomas and effects of Endostar on U251 cell. Pathol Res Pract 2011;207(10):645–51. DOI: 10.1016/J.PRP.2011.07.012</mixed-citation></ref><ref id="B14"><label>14.</label><mixed-citation>Gao Y., Zhao X.L., Gu Q. et al. Correlation of vasculogenic mimicry with clinicopathologic features and prognosis of ovarian carcinoma. Zhonghua Bing Li Xue Za Zhi 2009;38(9):585–9. (In Chinese). DOI: 10.3760/cma.j.issn.0529-5807.2009.09.003</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>Lim D., Do Y., Kwon B.S. et al. Angiogenesis and vasculogenic mimicry as therapeutic targets in ovarian cancer. BMB Rep 2020;53(6):291. DOI: 10.5483/BMBREP.2020.53.6.060</mixed-citation></ref><ref id="B16"><label>16.</label><mixed-citation>Van Der Schaft D.W.J., Hillen F., Pauwels P. et al. Tumor cell plasticity in Ewing sarcoma, an alternative circulatory system stimulated by hypoxia. Cancer Res 2005;65(24):11520–8. DOI: 10.1158/0008-5472.CAN-05-2468</mixed-citation></ref><ref id="B17"><label>17.</label><mixed-citation>Cesca K., Oliveira E.M. Confocal laser microscopy for VM analysis with DAPI and phalloidin staining. Methods Mol Biol 2022;2514:153–61. DOI: 10.1007/978-1-0716-2403-6_15</mixed-citation></ref><ref id="B18"><label>18.</label><mixed-citation>De Andrade Peixoto M., Marques dos Reis E., Marques Porto L. Cancer cell spheroids as a 3D model for exploring the pathobiology of vasculogenic mimicry. Methods Mol Biol 2022;2514:45–51. DOI: 10.1007/978-1-0716-2403-6_5</mixed-citation></ref><ref id="B19"><label>19.</label><mixed-citation>Kobayashi H., Shirakawa K., Kawamoto S. et al. Rapid accumulation and internalization of radiolabeled Herceptin in an inflammatory breast cancer xenograft with vasculogenic mimicry predicted by the contrast-enhanced dynamic MRI with the macromolecular contrast agent G6-(1B4M-Gd) 256. Cancer Res 2002;62(3):860–6.</mixed-citation></ref><ref id="B20"><label>20.</label><mixed-citation>Chen L., Zhang S., Li X. et al. A pilot study of vasculogenic mimicry immunohistochemical expression in intraocular melanoma model. Oncol Rep 2009;21(4):989–94. DOI: 10.3892/OR_00000313/HTML</mixed-citation></ref><ref id="B21"><label>21.</label><mixed-citation>Zhang S., Zhang D., Wang Y. et al. Morphologic research of microcirculation patterns in human and animal melanoma. Med Oncol 2005;23(3):403–9. DOI: 10.1385/MO:23:3:403</mixed-citation></ref><ref id="B22"><label>22.</label><mixed-citation>Angara K., Borin T.F., Arbab A.S. Vascular mimicry: a novel neovascularization mechanism driving anti-angiogenic therapy (AAT) resistance in glioblastoma. Transl Oncol 2017;10(4):650–60. DOI: 10.1016/j.tranon.2017.04.007</mixed-citation></ref><ref id="B23"><label>23.</label><mixed-citation>Delgado-Bellido D., Serrano-Saenz S., Fernández-Cortés M. et al. Vasculogenic mimicry signaling revisited: focus on non-vascular VE-cadherin. Mol Cancer 2017;16(1):1–14. DOI: 10.1186/S12943-017-0631-X</mixed-citation></ref><ref id="B24"><label>24.</label><mixed-citation>Clemente M., Pérez-Alenza M.D., Illera J.C. et al. Histological, immunohistological, and ultrastructural description of vasculogenic mimicry in canine mammary cancer. Vet Pathol 2010;47(2):265–74. DOI: 10.1177/0300985809353167</mixed-citation></ref><ref id="B25"><label>25.</label><mixed-citation>Folberg R., Maniotis A.J. Vasculogenic mimicry. APMIS 2004; 112(7–8):508–25. DOI: 10.1111/J.1600-0463.2004.APM11207-0810.X</mixed-citation></ref><ref id="B26"><label>26.</label><mixed-citation>Hendrix M.J.C., Seftor E.A., Hess A.R. et al. Vasculogenic mimicry and tumour-cell plasticity: lessons from melanoma. Nat Rev Cancer 2003;3(6):411–21. DOI: 10.1038/nrc1092</mixed-citation></ref><ref id="B27"><label>27.</label><mixed-citation>Hendrix M.J.C., Seftor E.A., Kirschmann D.A. et al. Remodeling of the microenvironment by aggressive melanoma tumor cells. Ann N Y Acad Sci 2003;995:151–61. DOI: 10.1111/j.1749-6632.2003.tb03218.x</mixed-citation></ref><ref id="B28"><label>28.</label><mixed-citation>Kirschmann D.A., Seftor E.A., Hardy K.M. et al. Molecular pathways: vasculogenic mimicry in tumor cells: diagnostic and therapeutic implications. Clin Cancer Res 2012;18(10):2726–32. DOI: 10.1158/1078-0432.CCR-11-3237</mixed-citation></ref><ref id="B29"><label>29.</label><mixed-citation>Sun B., Zhang S., Zhao X. et al. Vasculogenic mimicry is associated with poor survival in patients with mesothelial sarcomas and alveolar rhabdomyosarcomas. Int J Oncol 2004;25(6):1609–14. DOI: 10.3892/IJO.25.6.1609/HTML</mixed-citation></ref><ref id="B30"><label>30.</label><mixed-citation>McDonald D.M., Munn L., Jain R.K. Vasculogenic mimicry: how convincing, how novel, and how significant? Am J Pathol 2000;156(2):383. DOI: 10.1016/S0002-9440(10)64740-2</mixed-citation></ref><ref id="B31"><label>31.</label><mixed-citation>Huijbers E.J.M., Van Beijnum J.R., Thijssen V.L. et al. Role of the tumor stroma in resistance to anti-angiogenic therapy. Drug Resist Updat 2016;25:26–37. DOI: 10.1016/J.DRUP.2016.02.002</mixed-citation></ref><ref id="B32"><label>32.</label><mixed-citation>Riabov V., Gudima A., Wang N. et al. Role of tumor associated macrophages in tumor angiogenesis and lymphangiogenesis. Front Physiol 2014;5:75. DOI: 10.3389/FPHYS.2014.00075</mixed-citation></ref><ref id="B33"><label>33.</label><mixed-citation>Barnett F.H., Rosenfeld M., Wood M. et al. Macrophages form functional vascular mimicry channels in vivo. Sci Rep 2016;6:36659. DOI: 10.1038/SREP36659</mixed-citation></ref><ref id="B34"><label>34.</label><mixed-citation>Hutchenreuther J., Vincent K., Norley C.R. et al. Activation of cancer-associated fibroblasts is required for tumor neovascularization in a murine model of melanoma. Matrix Biol 2018;74:52–61. DOI: 10.1016/J.MATBIO.2018.06.003</mixed-citation></ref><ref id="B35"><label>35.</label><mixed-citation>Anderberg C., Pietras K. On the origin of cancer-associated fibroblasts. Cell Cycle 2009;8(10):1461–5. DOI: 10.4161/CC.8.10.8557</mixed-citation></ref><ref id="B36"><label>36.</label><mixed-citation>Yu Y., Xiao C.H., Tan L.D. et al. Cancer-associated fibroblasts induce epithelial-mesenchymal transition of breast cancer cells through paracrine TGF-β signalling. Br J Cancer 2014;110(3):724–32. DOI: 10.1038/BJC.2013.768</mixed-citation></ref><ref id="B37"><label>37.</label><mixed-citation>Heldin C.H., Rubin K., Pietras K. et al. High interstitial fluid pressure – an obstacle in cancer therapy. Nat Rev Cancer 2004;4(10): 806–13. DOI: 10.1038/nrc1456</mixed-citation></ref><ref id="B38"><label>38.</label><mixed-citation>Bittner M., Meltzer P., Chen Y. et al. Molecular classification of cutaneous malignant melanoma by gene expression profiling. Nature 2000;406(6795):536–40. DOI: 10.1038/35020115</mixed-citation></ref><ref id="B39"><label>39.</label><mixed-citation>Seftor E.A., Meltzer P.S., Schatteman G.C. et al. Expression of multiple molecular phenotypes by aggressive melanoma tumor cells: role in vasculogenic mimicry. Crit Rev Oncol Hematol 2002;44(1):17–27. DOI: 10.1016/S1040-8428(01)00199-8</mixed-citation></ref><ref id="B40"><label>40.</label><mixed-citation>Seftor E.A., Meltzer P.S., Kirschmann D.A. et al. Molecular determinants of human uveal melanoma invasion and metastasis. Clin Exp Metastasis 2002;19(3):233–46. DOI: 10.1023/A:1015591624171</mixed-citation></ref><ref id="B41"><label>41.</label><mixed-citation>Sun B., Zhang D., Zhao N. et al. Epithelial-to-endothelial transition and cancer stem cells: two cornerstones of vasculogenic mimicry in malignant tumors. Oncotarget 2017;8(18):30502. DOI: 10.18632/ONCOTARGET.8461</mixed-citation></ref><ref id="B42"><label>42.</label><mixed-citation>Velez D.O., Tsui B., Goshia T. et al. 3D collagen architecture induces a conserved migratory and transcriptional response linked to vasculogenic mimicry. Nature Commun 2017;8(1):1–12. DOI: 10.1038/s41467-017-01556-7</mixed-citation></ref><ref id="B43"><label>43.</label><mixed-citation>Li M., Gu Y., Zhang Z. et al. Vasculogenic mimicry: a new prognostic sign of gastric adenocarcinoma. Pathol Oncol Res 2009;16(2):259–66. DOI: 10.1007/S12253-009-9220-7</mixed-citation></ref><ref id="B44"><label>44.</label><mixed-citation>Lu X.S., Sun W., Ge C.Y. et al. Contribution of the PI3K/MMPs/Ln-5γ2 and EphA2/FAK/Paxillin signaling pathways to tumor growth and vasculogenic mimicry of gallbladder carcinomas. Int J Oncol 2013;42(6):2103–115. DOI: 10.3892/IJO.2013.1897/HTML</mixed-citation></ref><ref id="B45"><label>45.</label><mixed-citation>Liu X., He H., Zhang F. et al. m6A methylated EphA2 and VEGFA through IGF2BP2/3 regulation promotes vasculogenic mimicry in colorectal cancer via PI3K/AKT and ERK1/2 signaling. Cell Death Dis 2022;13(5):483. DOI: 10.1038/S41419-022-04950-2</mixed-citation></ref><ref id="B46"><label>46.</label><mixed-citation>Schnegg C.I., Yang M.H., Ghosh S.K. et al. Induction of vasculogenic mimicry overrides VEGF-A silencing and enriches stem-like cancer cells in melanoma. Cancer Res 2015;75(8):1682–90. DOI: 10.1158/0008-5472.CAN-14-1855/651621/AM/INDUCTION-OF-VASCULOGENIC-MIMICRY-OVERRIDES-VEGF-A</mixed-citation></ref><ref id="B47"><label>47.</label><mixed-citation>Valdivia A., Mingo G., Aldana V. et al. Fact or fiction, it is time for a verdict on vasculogenic mimicry? Front Oncol 2019;9:680. DOI: 10.3389/fonc.2019.00680</mixed-citation></ref><ref id="B48"><label>48.</label><mixed-citation>Williamson S.C., Metcalf R.L., Trapani F. et al. Vasculogenic mimicry in small cell lung cancer. Nat Commun 2016;7(1):1–14. DOI: 10.1038/ncomms13322</mixed-citation></ref><ref id="B49"><label>49.</label><mixed-citation>Liu T.J., Sun B.C., Zhao X.L. et al. CD133+ cells with cancer stem cell characteristics associates with vasculogenic mimicry in triple-negative breast cancer. Oncogene 2013;32(5):544–53. DOI: 10.1038/ONC.2012.85</mixed-citation></ref><ref id="B50"><label>50.</label><mixed-citation>Ren K., Yao N., Wang G. et al. Vasculogenic mimicry: a new prognostic sign of human osteosarcoma. Hum Pathol 2014;45(10): 2120–9. DOI: 10.1016/J.HUMPATH.2014.06.013</mixed-citation></ref><ref id="B51"><label>51.</label><mixed-citation>Tang N.N., Zhu H., Zhang H.J. et al. HIF-1α induces VE-cadherin expression and modulates vasculogenic mimicry in esophageal carcinoma cells. World J Gastroenterol 2914;20(47):17894–904. DOI: 10.3748/WJG.V20.I47.17894</mixed-citation></ref><ref id="B52"><label>52.</label><mixed-citation>Xiao T., Zhong W., Zhao J. et al. Polyphyllin I suppresses the formation of vasculogenic mimicry via Twist1/VE-cadherin pathway. Cell Death Dis 2018;9(9):906. DOI: 10.1038/S41419-018-0902-5</mixed-citation></ref><ref id="B53"><label>53.</label><mixed-citation>Yeo C., Lee H.J., Lee E.O. Serum promotes vasculogenic mimicry through the EphA2/VE-cadherin/AKT pathway in PC-3 human prostate cancer cells. Life Sci 2019;221:267–73. DOI: 10.1016/J.LFS.2019.02.043</mixed-citation></ref><ref id="B54"><label>54.</label><mixed-citation>Zhao N., Sun B.C., Sun T. et al. Hypoxia-induced vasculogenic mimicry formation via VE-cadherin regulation by Bcl-2. Med Oncol 2912;29(5):3599–607. DOI: 10.1007/S12032-012-0245-5</mixed-citation></ref><ref id="B55"><label>55.</label><mixed-citation>Chen L.X., He Y.J., Zhao S.Z. et al. Inhibition of tumor growth and vasculogenic mimicry by curcumin through down-regulation of the EphA2/PI3K/MMP pathway in a murine choroidal melanoma model. Cancer Biol Ther 2011;11(2):229–35. DOI: 10.4161/CBT.11.2.13842</mixed-citation></ref><ref id="B56"><label>56.</label><mixed-citation>Hess A.R., Margaryan N.V., Seftor E.A. et al. Deciphering the signaling events that promote melanoma tumor cell vasculogenic mimicry and their link to embryonic vasculogenesis: role of the Eph receptors. Dev Dyn 2007;236(12):3283–96. DOI: 10.1002/DVDY.21190</mixed-citation></ref><ref id="B57"><label>57.</label><mixed-citation>Margaryan N.V., Strizzi L., Abbott D.E. et al. EphA2 as a promoter of melanoma tumorigenicity. Cancer Biol Ther 2009;8(3):279. DOI: 10.4161/CBT.8.3.7485</mixed-citation></ref><ref id="B58"><label>58.</label><mixed-citation>Hess A.R., Seftor E.A., Seftor R.E.B. et al. Phosphoinositide 3-kinase regulates membrane type 1-matrix metalloproteinase (MMP) and MMP-2 activity during melanoma cell vasculogenic mimicry. Cancer Res 2003;63(16):4757–62.</mixed-citation></ref><ref id="B59"><label>59.</label><mixed-citation>Li Y., Sun B., Zhao X. et al. MMP-2 and MMP-13 affect vasculogenic mimicry formation in large cell lung cancer. J Cell Mol Med 2017;21(12):3741. DOI: 10.1111/JCMM.13283</mixed-citation></ref><ref id="B60"><label>60.</label><mixed-citation>Liu X., Fassett J., Wei Y., Chen Y. Regulation of DDAH1 as a potential therapeutic target for treating cardiovascular diseases. Evid Based Complement Alternat Med 2013;2:2013:619207. DOI: 10.1155/2013/619207</mixed-citation></ref><ref id="B61"><label>61.</label><mixed-citation>Seftor R.E.B., Seftor E.A., Koshikawa N. et al. Cooperative interactions of laminin 5 gamma2 chain, matrix metalloproteinase-2, and membrane type-1-matrix/metalloproteinase are required for mimicry of embryonic vasculogenesis by aggressive melanoma. Cancer Res 2001;61(17):6322–7.</mixed-citation></ref><ref id="B62"><label>62.</label><mixed-citation>Yodkeeree S., Chaiwangyen W., Garbisa S. et al. Curcumin, demethoxycurcumin and bisdemethoxycurcumin differentially inhibit cancer cell invasion through the down-regulation of MMPs and uPA. J Nutr Biochem 2009;20(2):87–95. DOI: 10.1016/j.jnutbio.2007.12.003</mixed-citation></ref><ref id="B63"><label>63.</label><mixed-citation>Sood A.K., Seftor E.A., Fletcher M.S. et al. Molecular determinants of ovarian cancer plasticity. Am J Pathol 2001;158(4):1279–88. DOI: 10.1016/S0002-9440(10)64079-5</mixed-citation></ref><ref id="B64"><label>64.</label><mixed-citation>Hess A.R., Postovit L.M., Margaryan N.V. et al. Focal adhesion kinase promotes the aggressive melanoma phenotype. Cancer Res 2005;65(21):9851–60. DOI: 10.1158/0008-5472.CAN-05-2172</mixed-citation></ref><ref id="B65"><label>65.</label><mixed-citation>Fu R., Du W., Ding Z. et al. HIF-1α promoted vasculogenic mimicry formation in lung adenocarcinoma through NRP1 upregulation in the hypoxic tumor microenvironment. Cell Death Disease 2021;12(4):1–11. DOI: 10.1038/s41419-021-03682-z</mixed-citation></ref><ref id="B66"><label>66.</label><mixed-citation>Li W., Zong S.Q., Shi Q. et al. Hypoxia-induced vasculogenic mimicry formation in human colorectal cancer cells: involvement of HIF-1α, claudin-4, and E-cadherin and vimentin. Sci Rep 2016;6:37534. DOI: 10.1038/SREP37534</mixed-citation></ref><ref id="B67"><label>67.</label><mixed-citation>Song Y.Y., Sun L.D., Liu M.L. et al. STAT3, p-STAT3 and HIF-1α are associated with vasculogenic mimicry and impact on survival in gastric adenocarcinoma. Oncol Lett 2014;8(1):431–7. DOI: 10.3892/OL.2014.2059</mixed-citation></ref><ref id="B68"><label>68.</label><mixed-citation>Sun W., Shen Z.Y., Zhang H. et al. Overexpression of HIF-1α in primary gallbladder carcinoma and its relation to vasculogenic mimicry and unfavourable prognosis. Oncol Rep 2012;27(6): 1990–2002. DOI: 10.3892/OR.2012.1746</mixed-citation></ref><ref id="B69"><label>69.</label><mixed-citation>Wang M., Zhao X., Zhu D. et al. HIF-1α promoted vasculogenic mimicry formation in hepatocellular carcinoma through LOXL2 up-regulation in hypoxic tumor microenvironment. J Exp Clin Cancer Res 2017;36(1):60. DOI: 10.1186/S13046-017-0533-1</mixed-citation></ref><ref id="B70"><label>70.</label><mixed-citation>Wu S., Cheng Z., Yu L. et al. [Expression of CD82/KAI1 and HIF-1α in non-small cell lung cancer and their relationship to vasculogenic mimicry]. Zhongguo Fei Ai Za Zhi 2011;14(12):918–25. DOI: 10.3779/J.ISSN.1009-3419.2011.12.04</mixed-citation></ref><ref id="B71"><label>71.</label><mixed-citation>Zhang J.G., Zhou H.M., Zhang X. et al. Hypoxic induction of vasculogenic mimicry in hepatocellular carcinoma: role of HIF-1α, RhoA/ROCK and Rac1/PAK signaling. BMC Cancer 2020;20(1):32. DOI: 10.1186/S12885-019-6501-8</mixed-citation></ref><ref id="B72"><label>72.</label><mixed-citation>Wang Y., Yang R., Wang X. et al. Evaluation of the correlation of vasculogenic mimicry, Notch4, DLL4, and KAI1/CD82 in the prediction of metastasis and prognosis in non-small cell lung cancer. Medicine 2018;97(52):e13817. DOI: 10.1097/MD.0000000000013817</mixed-citation></ref><ref id="B73"><label>73.</label><mixed-citation>Strizzi L., Postovit L.M., Margaryan N.V. et al. Nodal as a biomarker for melanoma progression and a new therapeutic target for clinical intervention. Expert Rev Dermatol 2009;4(1):67–78. DOI: 10.1586/17469872.4.1.67</mixed-citation></ref><ref id="B74"><label>74.</label><mixed-citation>Strizzi L., Hardy K.M., Seftor E.A. et al. Development and cancer: At the crossroads of Nodal and Notch signaling. Cancer Res 2009;69(18):7131. DOI: 10.1158/0008-5472.CAN-09-1199</mixed-citation></ref><ref id="B75"><label>75.</label><mixed-citation>Hardy K.M., Kirschmann D.A., Seftor E.A. et al. Regulation of the embryonic morphogen Nodal by Notch4 facilitates manifestation of the aggressive melanoma phenotype. Cancer Res 2010;70(24):10340–50. DOI: 10.1158/0008-5472.CAN-10-0705</mixed-citation></ref><ref id="B76"><label>76.</label><mixed-citation>Gong W., Sun B., Zhao X. et al. Nodal signaling promotes vasculogenic mimicry formation in breast cancer via the Smad2/3 pathway. Oncotarget 2016;7(43):70152. DOI: 10.18632/ONCOTARGET.12161</mixed-citation></ref><ref id="B77"><label>77.</label><mixed-citation>Zang M., Hu L., Zhang B. et al. Luteolin suppresses angiogenesis and vasculogenic mimicry formation through inhibiting Notch1-VEGF signaling in gastric cancer. Biochem Biophys Res Commun 2017;490(3):913–19. DOI: 10.1016/J.BBRC.2017.06.140</mixed-citation></ref><ref id="B78"><label>78.</label><mixed-citation>Hsu M.Y., Yang M.H., Schnegg C.I. et al. Notch3 signaling-mediated melanoma-endothelial crosstalk regulates melanoma stem-like cell homeostasis and niche morphogenesis. Lab Invest 2017;97(6):725–36. DOI: 10.1038/LABINVEST.2017.1</mixed-citation></ref><ref id="B79"><label>79.</label><mixed-citation>Han C., Sun B., Zhao X. et al. Phosphorylation of STAT3 promotes vasculogenic mimicry by inducing epithelial-to-mesenchymal transition in colorectal cancer. Technol Cancer Res Treat 2017;16(6):1209–19. DOI: 10.1177/1533034617742312</mixed-citation></ref><ref id="B80"><label>80.</label><mixed-citation>Sun T., Zhao N., Zhao X.L. et al. Expression and functional significance of Twist1 in hepatocellular carcinoma: its role in vasculogenic mimicry. Hepatology 2010;51(2):545–56. DOI: 10.1002/HEP.23311</mixed-citation></ref><ref id="B81"><label>81.</label><mixed-citation>Hulin J.A., Tommasi S., Elliot D., Mangoni A.A. Small molecule inhibition of DDAH1 significantly attenuates triple negative breast cancer cell vasculogenic mimicry in vitro. Biomed Pharmacother 2019;111:602–12. DOI: 10.1016/j.biopha.2018.12.117</mixed-citation></ref><ref id="B82"><label>82.</label><mixed-citation>Cabral-Pacheco G.A., Garza-Veloz I., Castruita-De la Rosa C. et al. The roles of matrix metalloproteinases and their inhibitors in human diseases. Int J Mol Sci 2020;21(24):1–53. DOI: 10.3390/IJMS21249739</mixed-citation></ref><ref id="B83"><label>83.</label><mixed-citation>Sharma N., Seftor R.E., Seftor E.A. et al. Prostatic tumor cell plasticity involves cooperative interactions of distinct phenotypic subpopulations: role in vasculogenic mimicry. Prostate 2002;50(3):189–201. DOI: 10.1002/PROS.10048</mixed-citation></ref><ref id="B84"><label>84.</label><mixed-citation>Noorolyai S., Shajari N., Baghbani E. et al. The relation between PI3K/AKT signalling pathway and cancer. Gene 2019;698:120–8. DOI: 10.1016/J.GENE.2019.02.076</mixed-citation></ref><ref id="B85"><label>85.</label><mixed-citation>Hendrix M.J.C., Seftor E.A., Meltzer P.S. et al. Expression and functional significance of VE-cadherin in aggressive human melanoma cells: role in vasculogenic mimicry. Proc Natl Acad Sci USA 2001;98(14):8018–23. DOI: 10.1073/PNAS.131209798</mixed-citation></ref><ref id="B86"><label>86.</label><mixed-citation>Ferrara N. Role of vascular endothelial growth factor in regulation of physiological angiogenesis. Am J Physiol Cell Physiol 2001;280(6):49–6. DOI: 10.1152/AJPCELL.2001.280.6.C1358</mixed-citation></ref><ref id="B87"><label>87.</label><mixed-citation>Hanahan D., Folkman J. Patterns and emerging mechanisms of the angiogenic switch during tumorigenesis. Cell 1996;86(3):353–64. DOI: 10.1016/S0092-8674(00)80108-7</mixed-citation></ref><ref id="B88"><label>88.</label><mixed-citation>Wang J.Y., Sun T., Zhao X.L. et al. Functional significance of VEGF-a in human ovarian carcinoma: role in vasculogenic mimicry. Cancer Biol Ther 2008;7(5):758–66. DOI: 10.4161/CBT.7.5.5765</mixed-citation></ref><ref id="B89"><label>89.</label><mixed-citation>Cheng N., Brantley D., Fang W.B. et al. Inhibition of VEGF-dependent multistage carcinogenesis by soluble EphA receptors. Neoplasia 2003;5(5):445–56. DOI: 10.1016/S1476-5586(03)80047-7</mixed-citation></ref><ref id="B90"><label>90.</label><mixed-citation>Frank N.Y., Schatton T., Kim S. et al. VEGFR-1 expressed by malignant melanoma-initiating cells is required for tumor growth. Cancer Res 2011;71(4):1474–85. DOI: 10.1158/0008-5472.CAN-10-1660</mixed-citation></ref><ref id="B91"><label>91.</label><mixed-citation>Serova M., Tijeras-Raballand A., Dos Santos C. et al. Everolimus affects vasculogenic mimicry in renal carcinoma resistant to sunitinib. Oncotarget 2016;7(25):38467–86. DOI: 10.18632/ONCOTARGET.9542</mixed-citation></ref><ref id="B92"><label>92.</label><mixed-citation>Sun H., Zhang D., Yao Z. et al. Anti-angiogenic treatment promotes triple-negative breast cancer invasion via vasculogenic mimicry. Cancer Biol Ther 2017;18(4):205–13. DOI: 10.1080/15384047.2017.1294288</mixed-citation></ref><ref id="B93"><label>93.</label><mixed-citation>Brown S., Teo A., Pauklin S. et al. Activin/Nodal signaling controls divergent transcriptional networks in human embryonic stem cells and in endoderm progenitors. Stem Cells 2011;20(8):1176–85. DOI: 10.1002/STEM.666</mixed-citation></ref><ref id="B94"><label>94.</label><mixed-citation>Topczewska J.M., Postovit L.M., Margaryan N.V. et al. Embryonic and tumorigenic pathways converge via Nodal signaling: role in melanoma aggressiveness. Nat Med 2006;12(8):925–32. DOI: 10.1038/NM1448</mixed-citation></ref><ref id="B95"><label>95.</label><mixed-citation>Jue C., Lin C., Zhisheng Z. et al. Notch1 promotes vasculogenic mimicry in hepatocellular carcinoma by inducing EMT signaling. Oncotarget 2017;8(2):2501. DOI: 10.18632/ONCOTARGET.12388</mixed-citation></ref><ref id="B96"><label>96.</label><mixed-citation>Lee S.L.C., Rouhi P., Dahl Jensen L. et al. Hypoxia-induced pathological angiogenesis mediates tumor cell dissemination, invasion, and metastasis in a zebrafish tumor model. Proc Natl Acad Sci USA 2009;106(46):19485–90. DOI: 10.1073/PNAS.0909228106</mixed-citation></ref><ref id="B97"><label>97.</label><mixed-citation>Wei X., Chen Y., Jiang X. et al. Mechanisms of vasculogenic mimicry in hypoxic tumor microenvironments. Mol Cancer 2021;20(1):1–18. DOI: 10.1186/s12943-020-01288-1</mixed-citation></ref><ref id="B98"><label>98.</label><mixed-citation>De Bock K., Mazzone M., Carmeliet P. Antiangiogenic therapy, hypoxia, and metastasis: risky liaisons, or not? Nat Rev Clin Oncol 2011;8(7):393–404. DOI: 10.1038/NRCLINONC.2011.83</mixed-citation></ref><ref id="B99"><label>99.</label><mixed-citation>Compernolle V., Brusselmans K., Acker T. et al. Loss of HIF-2alpha and inhibition of VEGF impair fetal lung maturation, whereas treatment with VEGF prevents fatal respiratory distress in premature mice. Nat Med 2002;8(7):702–10. DOI: 10.1038/NM721</mixed-citation></ref><ref id="B100"><label>100.</label><mixed-citation>Postovit L.M., Abbott D.E., Payne S.L. et al. Hypoxia/reoxygenation: a dynamic regulator of lysyl oxidase-facilitated breast cancer migration. J Cell Biochem 2008;103(5):1369–78. DOI: 10.1002/jcb.21517</mixed-citation></ref><ref id="B101"><label>101.</label><mixed-citation>Jin-lu M., Han S.X., Zhu Q. et al. Role of Twist in vasculogenic mimicry formation in hypoxic hepatocellular carcinoma cells in vitro. Biochem Biophys Res Commun 2011;408(4):686–91. DOI: 10.1016/J.BBRC.2011.04.089</mixed-citation></ref><ref id="B102"><label>102.</label><mixed-citation>Zhang S., Li M., Zhang D. et al. Hypoxia influences linearly patterned programmed cell necrosis and tumor blood supply patterns formation in melanoma. Lab Invest 2009;89(5):575–86. DOI: 10.1038/LABINVEST.2009.20</mixed-citation></ref><ref id="B103"><label>103.</label><mixed-citation>Sun B., Zhang D., Zhang S. et al. Hypoxia influences vasculogenic mimicry channel formation and tumor invasion-related protein expression in melanoma. Cancer Lett 2007;249(2):188–97. DOI: 10.1016/J.CANLET.2006.08.016</mixed-citation></ref><ref id="B104"><label>104.</label><mixed-citation>Quail D.F., Taylor M.J., Walsh L.A. et al. Low oxygen levels induce the expression of the embryonic morphogen Nodal. Mol Biol Cell 2011;22(24):4809–21. DOI: 10.1091/MBC.E11-03-0263</mixed-citation></ref><ref id="B105"><label>105.</label><mixed-citation>Luo H., Chen Z., Jin H. et al. Cyclooxygenase-2 up-regulates vascular endothelial growth factor via a protein kinase C pathway in non-small cell lung cancer. J Exp Clin Cancer Res 2011;30(1):6. DOI: 10.1186/1756-9966-30-6</mixed-citation></ref><ref id="B106"><label>106.</label><mixed-citation>Wu W.K.K., Yiu Sung J.J., Lee C.W. et al. Cyclooxygenase-2 in tumorigenesis of gastrointestinal cancers: an update on the molecular mechanisms. Cancer Lett 2010;295(1):7–16. DOI: 10.1016/J.CANLET.2010.03.015</mixed-citation></ref><ref id="B107"><label>107.</label><mixed-citation>Basu G.D., Liang W.S., Stephan D.A. et al. A novel role for cyclooxygenase-2 in regulating vascular channel formation by human breast cancer cells. Breast Cancer Res 2006;8(6):1–11. DOI: 10.1186/BCR1626/FIGURES/6</mixed-citation></ref><ref id="B108"><label>108.</label><mixed-citation>Rong X., Huang B., Qiu S. et al. Tumor-associated macrophages induce vasculogenic mimicry of glioblastoma multiforme through cyclooxygenase-2 activation. Oncotarget 2016;7(51):83976–86. DOI: 10.18632/ONCOTARGET.6930</mixed-citation></ref></ref-list></back></article>
