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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="review-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">I.P. Pavlov Journal of Higher Nervous Activity</journal-id><journal-title-group><journal-title xml:lang="en">I.P. Pavlov Journal of Higher Nervous Activity</journal-title><trans-title-group xml:lang="ru"><trans-title>Журнал высшей нервной деятельности им. И.П. Павлова</trans-title></trans-title-group></journal-title-group><issn publication-format="print">0044-4677</issn><issn publication-format="electronic">3034-5316</issn><publisher><publisher-name xml:lang="en">The Russian Academy of Sciences</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">652104</article-id><article-id pub-id-type="doi">10.31857/S0044467724010037</article-id><article-categories><subj-group subj-group-type="toc-heading"><subject>ОБЗОРЫ И ТЕОРЕТИЧЕСКИЕ СТАТЬИ</subject></subj-group><subj-group subj-group-type="article-type"><subject>Review Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Participation of the subventricular zone of the brain in the development of brain glioma</article-title><trans-title-group xml:lang="ru"><trans-title>Участие субвентрикулярной зоны мозга в развитии глиомы головного мозга</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Revishchin</surname><given-names>A. V.</given-names></name><name xml:lang="ru"><surname>Ревищин</surname><given-names>А. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>revishchin@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Pavlova</surname><given-names>G. V.</given-names></name><name xml:lang="ru"><surname>Павлова</surname><given-names>Г. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>revishchin@mail.ru</email><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/><xref ref-type="aff" rid="aff3"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Institute of Higher Nervous Activity and Neurophysiology, Russian Academy of Sciences</institution></aff><aff><institution xml:lang="ru">ФГБУН “Институт высшей нервной деятельности и нейрофизиологии Российской Академии Наук”</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">N.N. Burdenko National Medical Research Center of Neurosurgery, Ministry of Healthcare of Russia</institution></aff><aff><institution xml:lang="ru">ФГАУ “НМИЦ нейрохирургии им. академика Н. Н. Бурденко” Минздрава России</institution></aff></aff-alternatives><aff-alternatives id="aff3"><aff><institution xml:lang="en">Sechenov First Moscow State Medical University</institution></aff><aff><institution xml:lang="ru">Первый Московский государственный медицинский университет им. И. М. Сеченова</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2024-07-10" publication-format="electronic"><day>10</day><month>07</month><year>2024</year></pub-date><volume>74</volume><issue>1</issue><fpage>26</fpage><lpage>35</lpage><history><date date-type="received" iso-8601-date="2025-02-02"><day>02</day><month>02</month><year>2025</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2024, Russian Academy of Sciences</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2024, Российская академия наук</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="en">Russian Academy of Sciences</copyright-holder><copyright-holder xml:lang="ru">Российская академия наук</copyright-holder></permissions><self-uri xlink:href="https://innoscience.ru/0044-4677/article/view/652104">https://innoscience.ru/0044-4677/article/view/652104</self-uri><abstract xml:lang="en"><p>Glioblastoma (GBM) is a malignant tumor with an average survival rate of 15–16 months with standard treatment; however, cases of successful treatment provide hope that a better understanding of the pathology will improve prognosis. Glial tumors contain clonogenic cells (cells capable of forming colonies in a culture medium) with a high proliferative potential, and their descendants have a wide range of possible differentiation; these clonogenic cells are currently considered as glioma stem cells (GSCs). In normal and pathological conditions, there are zones in the adult brain that contain proliferating neural stem cells (NSCs) and their descendants – progenitor cells that have begun to differentiate. One such zone lying on the lateral wall of the lateral ventricle, called the subventricular zone of the lateral ventricle (SVZ), has attracted much attention due to its importance for gliomagenesis. Numerous studies have shown that the intense exchange of signaling molecules and cells between the GBM and the SVZ leads to accelerated tumor growth and an increased risk of relapse. Research results indicate the possibility of developing new, more effective strategies to combat this dangerous disease, taking into account knowledge about the role of SVZ in the development of this pathology.</p></abstract><trans-abstract xml:lang="ru"><p>Глиобластома (ГБМ) – злокачественная опухоль со средней выживаемостью 15–16 месяцев при стандартном лечении; однако случаи успешного лечения дают надежду на то, что более глубокое понимание патологии улучшит прогноз. Глиальные опухоли содержат клоногенные клетки (клетки, способные образовывать колонии в культуральной среде) с высоким пролиферативным потенциалом, а их потомки обладают широким спектром возможной дифференцировки; данные клоногенные клетки в настоящее время рассматриваются как стволовые клетки глиомы (ГСК). В норме и патологии во взрослом мозге существуют зоны, которые содержат пролиферирующие нейральные стволовые клетки (НСК) и их потомки – начавшие дифференцировку прогениторные клетки. Одна из таких зон, лежащая на латеральной стенке бокового желудочка, называемая субвентрикулярной зоной бокового желудочка (СВЗ), привлекает большое внимание в связи с ее значением для глиомогенеза. Многочисленные исследования показали, что интенсивный обмен сигнальными молекулами и клетками между ГБМ и СВЗ приводит к ускорению роста опухоли и повышению риска рецидивов. Результаты исследований указывают на возможности разработки новых, более действенных стратегий борьбы с этим опасным заболеванием с учетом знаний о роли СВЗ в развитии этой патологии.</p></trans-abstract><kwd-group xml:lang="en"><kwd>glioma</kwd><kwd>glioblastoma</kwd><kwd>subventricular zone</kwd><kwd>stem cell</kwd><kwd>neurogenesis</kwd><kwd>subventricular zone</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>глиома</kwd><kwd>глиобластома</kwd><kwd>субвентрикулярная зона</kwd><kwd>стволовая клетка</kwd><kwd>нейрогенез</kwd><kwd>субвентрикулярная зона</kwd></kwd-group><funding-group><award-group><funding-source><institution-wrap><institution xml:lang="ru">Минобрнауки России</institution></institution-wrap><institution-wrap><institution xml:lang="en">Ministry of Education and Science of Russia</institution></institution-wrap></funding-source><award-id>075–15–2021–1343</award-id></award-group></funding-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Корочкин Л. И., Ревищин A. B., Охотин В. Е. Нейральные стволовые клетки, их значение в восстановительных процессах в нервной системе. Морфология. 2005. 127 (3): 7–16.</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Павлова Г. В., Охотин В. Е., Корочкин Л. И., Ревищин А. В. Геномная регуляция судьбы нейральных стволовых клеток млекопитающих. Генетика. 2008. 44 (3): 293–299.</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Aboody K. S., Brown A., Rainov N. G., Bower K. A., Liu S., Yang W., Small J. E., Herrlinger U., Ourednik V., Black P. M., Breakefield X. O., and Snyder E. Y. Neural stem cells display extensive tropism for pathology in adult brain: evidence from intracranial gliomas. Proc Natl Acad Sci U S A. 2000. 97(23): 12846–12851.</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>Adeberg S., Bostel T., Konig L., Welzel T., Debus J., and Combs S. E. A comparison of long-term survivors and short-term survivors with glioblastoma, subventricular zone involvement: a predictive factor for survival? Radiat Oncol. 2014. 9 (95).</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>Ahmadipour Y., Krings J. I., Rauschenbach L., Gembruch O., Chihi M., Darkwah Oppong M., Pierscianek D., Jabbarli R., Sure U., and El Hindy N. The influence of subventricular zone involvement in extent of resection and tumor growth pattern of glioblastoma. Innov Surg Sci. 2020. 5 (3–4): 127–132.</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>Allport J. R., Shinde Patil V. R., and Weissleder R. Murine neuronal progenitor cells are preferentially recruited to tumor vasculature via alpha4-integrin and SDF-1alpha-dependent mechanisms. Cancer Biol Ther. 2004. 3 (9): 838–844.</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>Bergmann O., Liebl J., Bernard S., Alkass K., Yeung M. S., Steier P., Kutschera W., Johnson L., Landen M., Druid H., Spalding K. L., and Frisen J. The age of olfactory bulb neurons in humans. Neuron. 2012. 74 (4): 634–639.</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>Bexell D., Gunnarsson S., Nordquist J., and Bengzon J. Characterization of the subventricular zone neurogenic response to rat malignant brain tumors. Neuroscience, 2007. 147 (3): 824–832.</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>Burns M. J., and Weiss W. Targeted therapy of brain tumors utilizing neural stem and progenitor cells. Front Biosci. 2003. 8: 228–234.</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>Cao F., Hata R., Zhu P., Ma Y. J., Tanaka J., Hanakawa Y., Hashimoto K., Niinobe M., Yoshikawa K., and Sakanaka M. Overexpression of SOCS3 inhibits astrogliogenesis and promotes maintenance of neural stem cells. J Neurochem. 2006. 98 (2): 459–470.</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>Chen L., Guerrero-Cazares H., Ye X., Ford E., McNutt T., Kleinberg L., Lim M., Chaichana K., Quinones-Hinojosa A., and Redmond K. Increased subventricular zone radiation dose correlates with survival in glioblastoma patients after gross total resection. Int J Radiat Oncol Biol Phys. 2013. 86 (4): 616–622.</mixed-citation></ref><ref id="B12"><label>12.</label><mixed-citation>Doetsch F., Caille I., Lim D. A., Garcia-Verdugo J.M., and Alvarez-Buylla A. Subventricular zone astrocytes are neural stem cells in the adult mammalian brain. Cell. 1999. 97 (6): 703–716.</mixed-citation></ref><ref id="B13"><label>13.</label><mixed-citation>Ehtesham M., Winston J. A., Kabos P., and Thompson R. C. CXCR4 expression mediates glioma cell invasiveness. Oncogene. 2006. 25 (19): 2801–2806.</mixed-citation></ref><ref id="B14"><label>14.</label><mixed-citation>Ehtesham M., Yuan X., Kabos P., Chung N. H., Liu G., Akasaki Y., Black K. L., and Yu J. S. Glioma tropic neural stem cells consist of astrocytic precursors and their migratory capacity is mediated by CXCR4. Neoplasia. 2004. 6 (3): 287–293.</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>Ellingson B. M., Lai A., Harris R. J., Selfridge J. M., Yong W. H., Das K., Pope W. B., Nghiemphu P. L., Vinters H. V., Liau L. M., Mischel P. S., and Cloughesy T. F. Probabilistic radiographic atlas of glioblastoma phenotypes. AJNR Am J Neuroradiol. 2013. 34 (3): 533–540.</mixed-citation></ref><ref id="B16"><label>16.</label><mixed-citation>Eriksson P. S., Perfilieva E., Bjork-Eriksson T., Alborn A. M., Nordborg C., Peterson D. A., and Gage F. H. Neurogenesis in the adult human hippocampus. Nat Med. 1998. 4 (11): 1313–1317.</mixed-citation></ref><ref id="B17"><label>17.</label><mixed-citation>Ernst A., Alkass K., Bernard S., Salehpour M., Perl S., Tisdale J., Possnert G., Druid H., and Frisen J. Neurogenesis in the striatum of the adult human brain. Cell. 2014. 156 (5): 1072–1083.</mixed-citation></ref><ref id="B18"><label>18.</label><mixed-citation>Furth J., Kahn M. C., and Breedis C. The Transmission of Leukemia of Mice with a Single Cell. Am Journal Cancer. 1937. 31: (276–282.</mixed-citation></ref><ref id="B19"><label>19.</label><mixed-citation>Gage F. H., Ray J., and Fisher L. J. Isolation, characterization, and use of stem cells from the CNS. Annu Rev Neurosci. 1995. 18: 159–192.</mixed-citation></ref><ref id="B20"><label>20.</label><mixed-citation>Glass R., Synowitz M., Kronenberg G., Walzlein J. H., Markovic D. S., Wang L. P., Gast D., Kiwit J., Kempermann G., and Kettenmann H. Glioblastoma-induced attraction of endogenous neural precursor cells is associated with improved survival. J Neurosci. 2005. 25 (10): 2637–2646.</mixed-citation></ref><ref id="B21"><label>21.</label><mixed-citation>Gleeson J. G., Lin P. T., Flanagan L. A., and Walsh C. A. Doublecortin is a microtubule-associated protein and is expressed widely by migrating neurons. Neuron. 1999. 23 (2): 257–271.</mixed-citation></ref><ref id="B22"><label>22.</label><mixed-citation>Goffart N., Kroonen J., Di Valentin E., Dedobbeleer M., Denne A., Martinive P., and Rogister B. Adult mouse subventricular zones stimulate glioblastoma stem cells specific invasion through CXCL12/CXCR4 signaling. Neuro Oncol. 2015. 17 (1): 81–94.</mixed-citation></ref><ref id="B23"><label>23.</label><mixed-citation>Goffart N., Lombard A., Lallemand F., Kroonen J., Nassen J., Di Valentin E., Berendsen S., Dedobbeleer M., Willems E., Robe P., Bours V., Martin D., Martinive P., Maquet P., and Rogister B. CXCL12 mediates glioblastoma resistance to radiotherapy in the subventricular zone. Neuro Oncol. 2017. 19 (1): 66–77.</mixed-citation></ref><ref id="B24"><label>24.</label><mixed-citation>Gollapalli K., Ghantasala S., Kumar S., Srivastava R., Rapole S., Moiyadi A., Epari S., and Srivastava S. Subventricular zone involvement in Glioblastoma – A proteomic evaluation and clinicoradiological correlation. Sci Rep. 2017. 7 (1): 1449.</mixed-citation></ref><ref id="B25"><label>25.</label><mixed-citation>Gupta T., Nair V., Paul S. N., Kannan S., Moiyadi A., Epari S., and Jalali R. Can irradiation of potential cancer stem-cell niche in the subventricular zone influence survival in patients with newly diagnosed glioblastoma? J Neurooncol. 2012. 109 (1): 195–203.</mixed-citation></ref><ref id="B26"><label>26.</label><mixed-citation>Hira V. V.V., Molenaar R. J., Breznik B., Lah T., Aronica E., and Van Noorden C. J.F. Immunohistochemical Detection of Neural Stem Cells and Glioblastoma Stem Cells in the Subventricular Zone of Glioblastoma Patients. J Histochem Cytochem. 2021. 69 (5): 349–364.</mixed-citation></ref><ref id="B27"><label>27.</label><mixed-citation>Ichimura K., Ohgaki H., Kleihues P., and Collins V. P. Molecular pathogenesis of astrocytic tumours. J Neurooncol. 2004. 70 (2): 137–160.</mixed-citation></ref><ref id="B28"><label>28.</label><mixed-citation>Ignatova T. N., Kukekov V. G., Laywell E. D., Suslov O. N., Vrionis F. D., and Steindler D. A. Human cortical glial tumors contain neural stem-like cells expressing astroglial and neuronal markers in vitro. Glia. 2002. 39 (3): 193–206.</mixed-citation></ref><ref id="B29"><label>29.</label><mixed-citation>Jafri N. F., Clarke J. L., Weinberg V., Barani I. J., and Cha S. Relationship of glioblastoma multiforme to the subventricular zone is associated with survival. Neuro Oncol. 2013. 15 (1): 91–96.</mixed-citation></ref><ref id="B30"><label>30.</label><mixed-citation>Kam M., Curtis M. A., McGlashan S.R., Connor B., Nannmark U., and Faull R. L. The cellular composition and morphological organization of the rostral migratory stream in the adult human brain. J Chem Neuroanat. 2009. 37 (3): 196–205.</mixed-citation></ref><ref id="B31"><label>31.</label><mixed-citation>Kim J. E., Park J. E., Park S. Y., Kim Y. H., Hong C. K., Kim J. H., and Kim H. S. Defining subventricular zone involvement to predict the survival of patients in isocitrate dehydrogenase-wild type glioblastoma: validation in a prospective registry. Eur Radiol. 2023. 33 (9): 6448– 6458.</mixed-citation></ref><ref id="B32"><label>32.</label><mixed-citation>Kimura M., Lee Y., Miller R., and Castillo M. Glioblastoma multiforme: relationship to subventricular zone and recurrence. Neuroradiol J. 2013. 26 (5): 542–547.</mixed-citation></ref><ref id="B33"><label>33.</label><mixed-citation>Kornack D. R., and Rakic P. The generation, migra tion, and differentiation of olfactory neurons in the adult primate brain. Proc Natl Acad Sci U S A. 2001. 98 (8): 4752–4757.</mixed-citation></ref><ref id="B34"><label>34.</label><mixed-citation>Kroonen J., Nassen J., Boulanger Y. G., Provenzano F., Capraro V., Bours V., Martin D., Deprez M., Robe P., and Rogister B. Human glioblastoma-initiating cells invade specifically the subventricular zones and olfactory bulbs of mice after striatal injection. Int J Cancer. 2011. 129 (3): 574–585.</mixed-citation></ref><ref id="B35"><label>35.</label><mixed-citation>Kucia M., Reca R., Miekus K., Wanzeck J., Wojakowski W., Janowska-Wieczorek A., Ratajczak J., and Ratajczak M. Z. Trafficking of normal stem cells and metastasis of cancer stem cells involve similar mechanisms: pivotal role of the SDF-1CXCR4 axis. Stem Cells. 2005. 23 (7): 879–894.</mixed-citation></ref><ref id="B36"><label>36.</label><mixed-citation>Levison S. W., and Goldman J. E. Both oligodendrocytes and astrocytes develop from progenitors in the subventricular zone of postnatal rat forebrain. Neuron. 1993. 10 (2): 201–212.</mixed-citation></ref><ref id="B37"><label>37.</label><mixed-citation>Liu Q., Sanai N., Jin W. N., La Cava A., Van Kaer L., and Shi F. D. Neural stem cells sustain natural killer cells that dictate recovery from brain inflammation. Nat Neurosci. 2016. 19 (2): 243–252.</mixed-citation></ref><ref id="B38"><label>38.</label><mixed-citation>MacLeod G., Bozek D. A., Rajakulendran N., Monteiro V., Ahmadi M., Steinhart Z., Kushida M. M., Yu H., Coutinho F. J., Cavalli F. M.G., Restall I., Hao X., Hart T., Luchman H. A., Weiss S., Dirks P. B., and Angers S. Genome-Wide CRISPRCas9 Screens Expose Genetic Vulnerabilities and Mechanisms of Temozolomide Sensitivity in Glioblastoma Stem Cells. Cell Rep. 2019. 27 (3): 971–986 e979.</mixed-citation></ref><ref id="B39"><label>39.</label><mixed-citation>Matarredona E. R., and Pastor A. M. Neural Stem Cells of the Subventricular Zone as the Origin of Human Glioblastoma Stem Cells. Therapeutic Implications. Front Oncol. 2019. 9: 779.</mixed-citation></ref><ref id="B40"><label>40.</label><mixed-citation>Mattei V, Santilli F, Martellucci S, Delle Monache S, Fabrizi J, Colapietro A, Angelucci A, Festuccia C. The Importance of Tumor Stem Cells in Glioblastoma Resistance to Therapy. Int J Mol Sci. 2021. 22 (8): 3863. doi: 10.3390/ijms22083863.</mixed-citation></ref><ref id="B41"><label>41.</label><mixed-citation>Morshead C. M., Craig C. G., and van der Kooy D. In vivo clonal analyses reveal the properties of endogenous neural stem cell proliferation in the adult mammalian forebrain. Development. 1998. 125 (12): 2251–2261.</mixed-citation></ref><ref id="B42"><label>42.</label><mixed-citation>Pavlova G., Kolesnikova V., Samoylenkova N., Drozd S., Revishchin A., Shamadykova D., Usachev D. Y., and Kopylov A. A Combined Effect of G-Quadruplex and Neuro-Inducers as an Alternative Approach to Human Glioblastoma Therapy. Front Oncol. 2022. 12: 880740.</mixed-citation></ref><ref id="B43"><label>43.</label><mixed-citation>Quinones-Hinojosa A., Sanai N., Soriano-Navarro M., Gonzalez-Perez O., Mirzadeh Z., Gil-Perotin S., Romero-Rodriguez R., Berger M. S., Garcia-Verdugo J.M., and Alvarez-Buylla A. Cellular composition and cytoarchitecture of the adult human subventricular zone: a niche of neural stem cells. J Comp Neurol. 2006. 494 (3): 415–434.</mixed-citation></ref><ref id="B44"><label>44.</label><mixed-citation>Rempel S. A., Dudas S., Ge S., and Gutierrez J. A. Identification and localization of the cytokine SDF1 and its receptor, CXC chemokine receptor 4, to regions of necrosis and angiogenesis in human glioblastoma. Clin Cancer Res. 2000. 6 (1): 102–111.</mixed-citation></ref><ref id="B45"><label>45.</label><mixed-citation>Revishchin A. V., Korochkin L. I., Okhotin V. E., Pavlova G. V. Neural stem cells in the mammalian brain. Int Rev Cytol. 2008. 265: 55–109.</mixed-citation></ref><ref id="B46"><label>46.</label><mixed-citation>Ripari L. B., Norton E. S., Bodoque-Villar R., Jeanneret S., Lara-Velazquez M., Carrano A., Zarco N., Vazquez-Ramos C.A., Quinones-Hinojosa A., de la Rosa-Prieto C., and Guerrero-Cazares H. Glioblastoma Proximity to the Lateral Ventricle Alters Neurogenic Cell Populations of the Subventricular Zone. Front Oncol. 2021. 11: 650316.</mixed-citation></ref><ref id="B47"><label>47.</label><mixed-citation>Rizzo A. E., Yu J., Suh J., Emch T., Murphy E., Ahluwalia M., Reddy C., and S. Chao. Investigating the Relationship Between Radiation Dose to Neural Stem Cell Niches and Survival in GBM. Int J Radiat Oncol 2014. 90 (1S): S283-S284.</mixed-citation></ref><ref id="B48"><label>48.</label><mixed-citation>Rousselot P., Lois C., and Alvarez-Buylla A. Embryonic (PSA) N-CAM reveals chains of migrating neuroblasts between the lateral ventricle and the olfactory bulb of adult mice. J Comp Neurol. 1995. 351(1): 51–61.</mixed-citation></ref><ref id="B49"><label>49.</label><mixed-citation>Sanai N., Alvarez-Buylla A., and Berger M. S. Neural stem cells and the origin of gliomas. N Engl J Med. 2005. 353 (8): 811–822.</mixed-citation></ref><ref id="B50"><label>50.</label><mixed-citation>Sanai N., Berger M. S., Garcia-Verdugo J.M., and Alvarez-Buylla A. Comment on “Human neuroblasts migrate to the olfactory bulb via a lateral ventricular extension”. Science. 2007. 318 (5849): 393; author reply 393.</mixed-citation></ref><ref id="B51"><label>51.</label><mixed-citation>Sanai N., Tramontin A. D., Quinones-Hinojosa A., Barbaro N. M., Gupta N., Kunwar S., Lawton M. T., McDermott M.W., Parsa A. T., Manuel-Garcia Verdugo J., Berger M. S., and Alvarez-Buylla A. Unique astrocyte ribbon in adult human brain contains neural stem cells but lacks chain migration. Nature. 2004. 427 (6976): 740–744.</mixed-citation></ref><ref id="B52"><label>52.</label><mixed-citation>Staflin K., Honeth G., Kalliomaki S., Kjellman C., Edvardsen K., and Lindvall M. Neural progenitor cell lines inhibit rat tumor growth in vivo. Cancer Res. 2004. 64 (15): 5347–5354.</mixed-citation></ref><ref id="B53"><label>53.</label><mixed-citation>Susman S., Leucuta D. C., Kacso G., and Florian S. I. High dose vs low dose irradiation of the subventricular zone in patients with glioblastoma-a systematic review and meta-analysis. Cancer Manag Res. 2019. 11: 6741–6753.</mixed-citation></ref><ref id="B54"><label>54.</label><mixed-citation>Wang C., Liu F., Liu Y.Y., Zhao C.H., You Y., Wang L., Zhang J., Wei B., Ma T., Zhang Q., Zhang Y., Chen R., Song H., Yang Z. Identification and characterization of neuroblasts in the subventricular zone and rostral migratory stream of the adult human brain. Cell Res. 2011. 21 (11): 1534–1550.</mixed-citation></ref><ref id="B55"><label>55.</label><mixed-citation>Wang C., You Y., Qi D., Zhou X., Wang L., Wei S., Zhang Z., Huang W., Liu Z., Liu F., Ma L., and Yang Z. Human and monkey striatal interneurons are derived from the medial ganglionic eminence but not from the adult subventricular zone. J Neurosci. 2014. 34 (33): 10906–10923.</mixed-citation></ref><ref id="B56"><label>56.</label><mixed-citation>Weinstein D. E., Shelanski M. L., and Liem R. K. C17, a retrovirally immortalized neuronal cell line, inhibits the proliferation of astrocytes and astrocytoma cells by a contact-mediated mechanism. Glia. 1990. 3 (2): 130–139.</mixed-citation></ref><ref id="B57"><label>57.</label><mixed-citation>Yip S., Aboody K. S., Burns M., Imitola J., Boockvar J. A., Allport J., Park K. I., Teng Y. D., Lachyankar M., McIntosh T., O’Rourke D.M., Khoury S., Weissleder R., Black P. M., Weiss W., and Snyder E. Y. Neural stem cell biology may be well suited for improving brain tumor therapies. Cancer J. 2003. 9 (3): 189–204.</mixed-citation></ref><ref id="B58"><label>58.</label><mixed-citation>Zhang J., Sarkar S., and Yong V. W. The chemokine stromal cell derived factor-1 (CXCL12) promotes glioma invasiveness through MT2-matrix metalloproteinase. Carcinogenesis. 2005. 26 (12): 2069–2077.</mixed-citation></ref><ref id="B59"><label>59.</label><mixed-citation>Zhang S., and Cui W. Sox2, a key factor in the regulation of pluripotency and neural differentiation. World J Stem Cells. 2014. 6 (3): 305–311.</mixed-citation></ref><ref id="B60"><label>60.</label><mixed-citation>Zhang S., Zhao F., Zhou T., Liu D., Yao X., Fu W., Liu Z., Lan C., Lai Z., Liu C., Li H., Li Y., Hu S., Yin Y., Tan L., Li W., Li F., Hu R., and Feng H. Combination of the Distance From Tumor Edge to Subventricular Zone and IDH Mutation Predicts Prognosis of Patients With Glioma. Front Oncol. 2021. 11: 693693.</mixed-citation></ref></ref-list></back></article>
