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IL-17 induces the proliferation and migration of glioma cells through the activation of PI3K/Akt1/NF-?B-p65 | Abstract
Journal of Molecular Imaging & Dynamics

Journal of Molecular Imaging & Dynamics
Open Access

ISSN: 2155-9937

+44-151-808-0171

Abstract

IL-17 induces the proliferation and migration of glioma cells through the activation of PI3K/Akt1/NF-?B-p65

Wen Qiu

Interleukin 17 (IL?17), as a pro-inflammatory cytokine, is up-regulated in the sera and tumor tissues of glioma patients; however the effects of IL-17 on glioma proliferation and migration remain unclear. In this study, the roles of IL-17 in the proliferation and migration of glioma cells and their potential mechanisms were determined. The results showed that IL-17 could not only enhance the proliferation and migration of cultured glioma cells (in vitro), but also promote the tumor formation of glioma cells in BALB/c nude mice (in vivo). Mechanical exploration revealed that IL-17 stimulation could increase the phosphorylation levels of Akt1 and NF-κ B-p65 in glioma cells, and knockdown or inhibition of PI3K, Akt1 and NF-κ B-p65 could also reduce the IL-17-induced proliferation and migration of the glioma cells. Moreover, PI3K/Akt1 was the upstream regulator of NF-κ B-p65 activation in IL-17-incubated glioma cells. Furthermore, the inhibition of PI3K, Akt1 and NF-κ B-p65 markedly suppressed the tumor formation of glioma cells induced by IL-17. Together, these data indicate that IL-17 can promote the proliferation and migration of glioma cells via PI3K/Akt1/NF-κ B-p65 activation, and these findings might provide a new insight into glioma pathogenesis.

Published Date: 2021-03-22;

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