Abstract
Stem cells have been accredited for their contribution towards tissue repair and regeneration, however, their potential to cause cancer is given more attention. CD133, a glioma stem cell marker has been linked to brain tumour proliferation and multi-drug resistance. Failure of CD133+ cells to define tumour relapse and an effective tumour forming ability of CD133– cells enhances the need to identify a selective and reliable stem cell marker. This review focuses on the undifferentiated and differentiated aspects of stem cells involving embryonic stem cell markers Oct4A and BMP2. In addition, alternative molecular targets have been enlisted that may help to further locate and eliminate tumour-initiating cells, thereby increasing the effectiveness of therapeutic drugs used to cure glioma.
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Khan, Z., Shervington, L., Shervington, A. (2012). Is CD133 the Appropriate Stem Cell Marker for Glioma?. In: Hayat, M. (eds) Stem Cells and Cancer Stem Cells, Volume 1. Stem Cells and Cancer Stem Cells, vol 1. Springer, Dordrecht. https://doi.org/10.1007/978-94-007-1709-1_13
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DOI: https://doi.org/10.1007/978-94-007-1709-1_13
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