Cancer Letters
Volume 291, Issue 2 , Pages 150-157, 28 May 2010

Isolation of cancer stem-like cells from a side population of a human glioblastoma cell line, SK-MG-1

  • Raita Fukaya

      Affiliations

    • Department of Neurosurgery, Keio University School of Medicine, Tokyo, Japan
  • ,
  • Shigeki Ohta

      Affiliations

    • Division of Cellular Signaling, Institute for Advanced Medical Research, Keio University School of Medicine, Tokyo Japan
  • ,
  • Masayuki Yamaguchi

      Affiliations

    • Functional Imaging Division, Research Center for Innovative Oncology, National Cancer Center Hospital East, Kashiwa, Japan
  • ,
  • Hirofumi Fujii

      Affiliations

    • Functional Imaging Division, Research Center for Innovative Oncology, National Cancer Center Hospital East, Kashiwa, Japan
  • ,
  • Yutaka Kawakami

      Affiliations

    • Division of Cellular Signaling, Institute for Advanced Medical Research, Keio University School of Medicine, Tokyo Japan
  • ,
  • Takeshi Kawase

      Affiliations

    • Department of Neurosurgery, Keio University School of Medicine, Tokyo, Japan
  • ,
  • Masahiro Toda

      Affiliations

    • Department of Neurosurgery, Keio University School of Medicine, Tokyo, Japan
    • Corresponding Author InformationCorresponding author. Address: Department of Neurosurgery, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan. Tel.: +81 3 5363 3587; fax: +81 3 5363 3862.

Received 1 December 2008; received in revised form 8 September 2009; accepted 13 October 2009. published online 16 November 2009.

Abstract 

Accumulating evidence suggests that in several types of brain tumors, including glioma, only a phenotypic subset of tumor cells called brain cancer stem cells (BCSCs) may be capable of initiating tumor growth. Recently, the isolation of side population (SP) cells using Hoechst dye has become a useful method for obtaining cancer stem cells in various tumors. In this study, we isolated cancer stem-like cells from human glioma cell lines using the SP technique. Flow cytometry analysis revealed that SK-MG-1, a human glioblastoma cell line, contained the largest number of SP cells among the five glioma cell lines that were analyzed. The SP cells had a self-renewal ability and were capable of forming spheres in a neurosphere culture medium containing EGF and FGF2. Spheres derived from the SP cells differentiated into three different lineage cells: neurons, astrocytes and oligodendrocytes. RT-PCR analysis revealed that the SP cells expressed a neural stem cell marker, Nestin. The SP cells generated tumors in the brains of NOD/SCID mice at 8weeks after implantation, whereas the non-SP cells did not generate any tumors in the brain. These results indicate that SP cells isolated from SK-MG-1 possess the properties of cancer stem cells, including their self-renewal ability, multi-lineage differentiation, and tumorigenicity. Therefore, the SP cells from SK-MG-1 may be useful for analyzing BCSCs because of the ease with which they can be handled and their yield.

Keywords: Brain cancer stem cell, Side population, Glioblastoma

Abbreviations: BCSC, brain cancer stem cell, SP, side population, EGF, epidermal growth factor, FGF2, fibroblast growth factor 2, WHO, World Health Organization, FBS, fetal bovine serum

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PII: S0304-3835(09)00632-6

doi:10.1016/j.canlet.2009.10.010

Cancer Letters
Volume 291, Issue 2 , Pages 150-157, 28 May 2010