| Literature DB >> 30405821 |
Yijun Qi1, Wendi Zhao2, Zhengguang Wang1, Qingsong Xie1, Jing Cao3, Xiangling Meng1.
Abstract
The Sonic hedgehog (Shh) signaling pathway may be interrelated with other signaling pathways, such as the phosphoinositide 3-kinase (PI3K) and mitogen-activated protein kinase (MAPK) pathways in gastrointestinal stromal tumor (GIST). The present study investigated the interaction among Shh, PI3K and MAPK signaling pathways in GIST cells. The expression of PI3K, MAPK and Shh signaling pathways in GIST-H1 cells were upregulated by endothelial growth factor (EGF) and recombinant Shh (N-shh) stimulation, and were downregulated by specific inhibitors of each signaling pathway. The proliferation rate of GIST-H1 cells were significantly increased under EGF or N-shh treatment (P<0.01). In addition, this effect was partially prevented by the pretreatment of the inhibitors of these signaling pathways. In summary, a cross regulation exists among the Shh, PI3K and MAPK signaling pathways in GIST-H-1 cells. The combined use of the inhibitors of these signaling pathways is a potentially novel option for GIST targeted therapy.Entities:
Keywords: Imatinib-resistance; Sonic hedgehog; gastrointestinal stromal tumor; mitogen-activated protein kinase; phosphoinositide 3-kinase
Year: 2018 PMID: 30405821 PMCID: PMC6202513 DOI: 10.3892/ol.2018.9494
Source DB: PubMed Journal: Oncol Lett ISSN: 1792-1074 Impact factor: 2.967