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Isolation of glioma cancer stem cells in relation to histological grades in glioma specimens
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  • 作者:Byung Ho Kong (1)
    Na-Ri Park (2)
    Jin-Kyoung Shim (3)
    Bo-Kyung Kim (3)
    Hye-Jin Shin (2)
    Ji-Hyun Lee (3)
    Yong-Min Huh (4)
    Su-Jae Lee (5)
    Se-Hoon Kim (6)
    Eui-Hyun Kim (3)
    Eun-Kyung Park (3)
    Jong Hee Chang (3)
    Dong-Seok Kim (3)
    Sun Ho Kim (3)
    Yong-Kil Hong (2)
    Seok-Gu Kang (3)
    Frederick F. Lang (7)
  • 关键词:Glioma ; Glioma cancer stem cell ; Gliomasphere ; Histological grade ; Isolation
  • 刊名:Child's Nervous System
  • 出版年:2013
  • 出版时间:February 2013
  • 年:2013
  • 卷:29
  • 期:2
  • 页码:217-229
  • 全文大小:690KB
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  • 作者单位:Byung Ho Kong (1)
    Na-Ri Park (2)
    Jin-Kyoung Shim (3)
    Bo-Kyung Kim (3)
    Hye-Jin Shin (2)
    Ji-Hyun Lee (3)
    Yong-Min Huh (4)
    Su-Jae Lee (5)
    Se-Hoon Kim (6)
    Eui-Hyun Kim (3)
    Eun-Kyung Park (3)
    Jong Hee Chang (3)
    Dong-Seok Kim (3)
    Sun Ho Kim (3)
    Yong-Kil Hong (2)
    Seok-Gu Kang (3)
    Frederick F. Lang (7)

    1. Department of Medical Science, The Catholic University of Korea College of Medicine, Seoul, South Korea
    2. Department of Neurosurgery, Seoul St. Mary’s Hospital, The Catholic University of Korea College of Medicine, Seoul, South Korea
    3. Department of Neurosurgery, Severance Hospital, Yonsei University College of Medicine, 50 Yonsei-ro, Seodaemun-gu, Seoul, 120-752, South Korea
    4. Department of Radiology, Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea
    5. Department of Chemistry, Hanyang University, Seoul, South Korea
    6. Department of Pathology, Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea
    7. Department of Neurosurgery, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA
  • ISSN:1433-0350
文摘
Purpose The existence of cancer stem cells (CSCs) in glioblastoma has been proposed. However, the unknown knowledge that is yet to be revealed is the presence of glioma CSCs (gCSCs) in correlation to each WHO grades of glioma. We approached this study with a hypothesis that specimens from high-grade gliomas would have higher isolation rate of gCSCs in comparison to those of lower-grade gliomas. Methods The glioma specimens were obtained from patients and underwent gliomasphere assay. The gliomaspheres were chosen to be analyzed with immunocytochemisty for surface markers. Then the selected gliomaspheres were exposed to neural differentiation conditions. Lastly, we made mouse orthotopic glioma models to examine the capacity of gliomagenesis. Results The gliomaspheres were formed in WHO grade IV (13 of 21) and III (two of nine) gliomas. Among them, WHO grade IV (11 of 13) and III (two of two) gliomaspheres showed similar surface markers to gCSCs and were capable of neural differentiation. Lastly, among the chosen cells, 10 of 11 WHO grade IV and two of two WHO grade III gliomaspheres were capable of gliomagenesis. Thus, overall, the rates of existence of gCSCs were more prominent in high-grade gliomas: 47.6?% (10 of 21) in WHO grade IV gliomas and 22.2?% (two of nine) in WHO grade III gliomas, whereas WHO grade II and I gliomas showed virtually no gCSCs. Conclusions This trend of stage-by-stage increase of gCSCs in gliomas showed statistical significance by chi-square test linear-by-linear association. We prove that the rates of existence of gCSCs increase proportionally as the WHO grades of gliomas rise.

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