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Gallic acid suppresses cell viability, proliferation, invasion and angiogenesis in human glioma cells

Open access
Lu, Yong, Jiang, Feng, Jiang, Hao, Wu, Kalina, Zheng, Xuguang, Cai, Yizhong, Katakowski, Mark, Chopp, Michael, To, Shing-Shun Tony·2010·European Journal of Pharmacology

Abstract

Gallic acid, an organic acid, also known as 3,4,5-trihydroxybenzoic acid, is cytotoxic against certain cancer cells, without harming normal cells. The objective of this study is to evaluate whether gallic acid can inhibit glioma cell viability, proliferation, invasion and reduce glioma cell mediated angiogenesis. Treatment of U87 and U251n glioma cells with gallic acid inhibited cell viability in a dose- and time-dependent manner. BrdU and tube formation assays indicated that gallic acid significantly decreased glioma cell proliferation and tube formation in mouse brain endothelial cells, respectively. In addition, gallic acid decreased U87 cell invasion in vitro. Western blot analysis showed that expression of ADAM17, p-Akt and p-Erk was suppressed by gallic acid in both U87 and U251n cell lines. These data suggest that suppression of ADAM17 and downregulation of PI3K/Akt and Ras/MAPK signaling pathways may contribute to gallic acid-induced decrease of invasiveness. Gallic acid may be a valuable candidate for treatment of brain tumor.

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Metadata

Authors
Lu, Y., Jiang, F., Jiang, H., Wu, K., Zheng, X., Cai, Y., Katakowski, M., Chopp, M., & To, S.-S. T.
Venue
European Journal of Pharmacology
Publisher
Elsevier BV
Published
2010-09
Volume
641
Issue
2-3
Pages
102-107
ISSN
0014-2999 (ISSN-L)
OpenAlex
W1965909855
Cited by
220
References
0
FWCI
4.15
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Gallic acid suppresses cell viability, proliferation, invasion and angiogenesis in human glioma cells. https://app.cochat.ai/papers/10.1016/j.ejphar.2010.05.043
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Lu, Y., Jiang, F., Jiang, H., Wu, K., Zheng, X., Cai, Y., Katakowski, M., Chopp, M., & To, S.-S. T. (2010). Gallic acid suppresses cell viability, proliferation, invasion and angiogenesis in human glioma cells. European Journal of Pharmacology. https://doi.org/10.1016/j.ejphar.2010.05.043

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