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Whether CD44 is an applicable marker for glioma stem cells
Hsiao-Han Wang1, Chen-Chieh Liao2, Nan-Haw Chow3,4
1Institute of Basic Medical Sciences, College of Medicine, National Cheng Kung UniversityTainan, Taiwan.
American Journal of Translational Research
|December 9, 2017
Summary
CD44 is not a reliable marker for glioma stem cells (GSCs). Low CD44 expression correlates with GSC traits, while CD44 may be more involved in tumor invasion and migration.
Area of Science:
- Neuro-oncology
- Cancer Biology
- Cell Biology
Background:
- Glioblastoma multiforme (GBM) is a highly aggressive brain tumor.
- Hyaluronan (HA) and its receptor CD44 are implicated in GBM.
- CD44 is often considered a cancer stem cell (CSC) marker, but conflicting data exists regarding its role in glioma stem cells (GSCs).
Purpose of the Study:
- To investigate the role of CD44 as a marker for glioma stem cells (GSCs).
- To determine if CD44 expression levels correlate with GSC properties and patient prognosis.
Main Methods:
- Manipulated CD44 expression in glioma cells using CD44 knockdown (CD44kd) and HA supplementation (HA+).
- Assessed cell proliferation, cell cycle progression, differentiation markers (GFAP), sphere formation, and stem cell markers (CD133, nestin, Oct4).
- Examined CD44 expression at the invasive rim of rat glioma specimens.
Main Results:
- CD44kd suppressed cell proliferation and induced GSC traits, including reduced GFAP and increased sphere formation and stem cell marker expression.
- HA+ treatment, which reduced CD44 expression, also increased GSC properties.
- Conversely, HA+ facilitated differentiation in GSC-like cells.
- CD44 was preferentially expressed at the invasive rim of gliomas.
Conclusions:
- CD44 is not an appropriate marker for identifying GSCs, as CD44-low cells exhibit more GSC traits.
- CD44 expression may be more critical for glioma cell invasion and migration than for maintaining stemness.

