Tamoxifen-induced apoptosis of rat C6 glioma cells via PI3K/Akt, JNK and ERK activation

  • Authors:
    • Ying Feng
    • Jintao Huang
    • Ying Ding
    • Fukang Xie
    • Xiaoyan Shen
  • View Affiliations

  • Published online on: December 1, 2010     https://doi.org/10.3892/or_00001018
  • Pages: 1561-1567
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Abstract

To elucidate the mechanism of TAM treatment on gliomas, we hypothesised that PI3K/Akt and MAPK signaling pathway may play important roles on TAM-induced apoptosis in C6 glioma cells. Our results demonstrated that TAM induced apoptosis of C6 glioma cells in a dose-dependent manner. The activation of AKT significantly decreased in a time-dependent manner in response to TAM treatment, JNK was transiently activated, and subsequently decreased activation and kept stable level, whereas ERK evidenced sustained activations in response to the drug treatment. The inhibition of PI3K/Akt and JNK both accelerated and enhanced TAM-induced apoptosis and ERK inhibition apparently exerted negative effect on apoptosis. We also observed that PI3K/Akt had intimate association with JNK and ERK activation in TAM-induced apoptosis. These findings may provide strategies for the molecularly targeted therapy in malignant gliomas.

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December 2010
Volume 24 Issue 6

Print ISSN: 1021-335X
Online ISSN:1791-2431

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Spandidos Publications style
Feng Y, Huang J, Ding Y, Xie F and Shen X: Tamoxifen-induced apoptosis of rat C6 glioma cells via PI3K/Akt, JNK and ERK activation . Oncol Rep 24: 1561-1567, 2010
APA
Feng, Y., Huang, J., Ding, Y., Xie, F., & Shen, X. (2010). Tamoxifen-induced apoptosis of rat C6 glioma cells via PI3K/Akt, JNK and ERK activation . Oncology Reports, 24, 1561-1567. https://doi.org/10.3892/or_00001018
MLA
Feng, Y., Huang, J., Ding, Y., Xie, F., Shen, X." Tamoxifen-induced apoptosis of rat C6 glioma cells via PI3K/Akt, JNK and ERK activation ". Oncology Reports 24.6 (2010): 1561-1567.
Chicago
Feng, Y., Huang, J., Ding, Y., Xie, F., Shen, X." Tamoxifen-induced apoptosis of rat C6 glioma cells via PI3K/Akt, JNK and ERK activation ". Oncology Reports 24, no. 6 (2010): 1561-1567. https://doi.org/10.3892/or_00001018