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Induction of neural differentiation in rat C6 glioma cells with taxol
Abstract
Background: Glioblastoma is a common and aggressive type of primary brain tumor. Several anticancer drugs affect GBM (glioblastoma multiforme) cells on cell growth and morphology. Taxol is one of the widely used antineoplastic drugs against many types of solid tumors, such as breast, ovarian, and prostate cancers. However, the effect of taxol on GBM cells remains unclear and requires further investigation. Methods: Survival rate of C6 glioma cells under different taxol concentrations was quantified. To clarify the differentiation patterns of rat C6 glioma cells under taxol challenge, survived glioma cells were characterized by immunocytochemical, molecular biological, and cell biological approaches. Results: After taxol treatment, not only cell death but also morphological changes, including cell elongation, cellular processes thinning, irregular shapes, and fragmented nucleation or micronuclei, occurred in the survived C6 cells. Neural differentiation markers NFL (for neurons), βIII‐tubulin (for neurons), GFAP (for astrocytes), and CNP ase (for oligodendrocytes) were detected in the taxol‐treated C6 cells. Quantitative analysis suggested a significant increase in the percentage of neural differentiated cells. The results exhibited that taxol may trigger neural differentiation in C6 glioma cells. Increased expression of neural differentiation markers in C6 cells after taxol treatment suggest that some anticancer drugs could be applied to elimination of the malignant cancer cells as well as changing proliferation and differentiation status of tumor cells.
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The pattern of GFAP upregulation by LDL is consistent with previous reports that deleterious stimuli induce GFAP expression in C6 cells, supporting the interpretation that LDL triggers a classical astrocytic stress response.
“This pattern is consistent with previous reports showing that deleterious stimuli induce GFAP expression in C6 cells (Shu et al. 2011; Chao et al. 2015), supporting the interpretation that LDL triggers a classical astrocytic stress response.”
From LDL Cholesterol Modulates Astrocyte Metabolism, Lipid Handling, and Morphology: Evidence From In Vitro and In Vivo Models (2026) · cites this paper as Chao et al. 2015
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Cited by
Sorted by citations
Baumart, G. J., Rodrigues, M. S., Sholl, J. N., de Sousa, A. C., Weber, A. F., Costa‐Beber, L. C., Farias, H. R., Costa, M. V., Peres, A. M., de Camargo, P. R., et al. (2026) · Journal of Neurochemistry · doi:10.1111/jnc.70403 · Cited by 2
Metadata
- Authors
- Chao, C., Kan, D., Lo, T., Lu, K., & Chien, C.
- Affiliations
- Department of Anatomy and Cell Biology College of Medicine National Taiwan University Taipei Taiwan
- Center of Genomic Medicine National Taiwan University Taipei Taiwan
- Venue
- Brain and Behavior
- Publisher
- Wiley
- Published
- 2015-10-26
- Volume
- 5
- Issue
- 12
- ISSN
- 2162-3279
- PMC
- PMC4667627
- Cited by
- 28
- References
- 0
- Language
- en
- Funders
- Ministry of Science and Technology Taiwan (NSC 100-2320-B-002-085)
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