Orai1 mediates tumor-promoting store-operated Ca entry in human gastrointestinal stromal tumors via c-KIT and the extracellular signal–regulated kinase pathway

Gastrointestinal stromal tumors originate from interstitial cells of Cajal, the pacemaker cells of the gut. Ca 2+ regulates the pacemaker activity of interstitial cells of Cajal. Store-operated Ca 2+ entry mediates the majority of Ca 2+ entry in most cancer cells and may be a factor in regulating in...

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Bibliographic Details
Published inTumor biology Vol. 39
Main Authors Lei Wang, Jiaqi Hao, Yijian Zhang, Ziyi Yang, Yang Cao, Wei Lu, Yijun Shu, Lin Jiang, Yunping Hu, Wenjie Lv, Yingbin Liu, Ping Dong
Format Journal Article
LanguageEnglish
Published IOS Press 01.02.2017
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Summary:Gastrointestinal stromal tumors originate from interstitial cells of Cajal, the pacemaker cells of the gut. Ca 2+ regulates the pacemaker activity of interstitial cells of Cajal. Store-operated Ca 2+ entry mediates the majority of Ca 2+ entry in most cancer cells and may be a factor in regulating intracellular Ca 2+ in interstitial cells of Cajal and gastrointestinal stromal tumors. Therefore, a blockade of this mechanism may affect the progression of gastrointestinal stromal tumors. Orai1 is the pore subunit of store-operated Ca 2+ channels. Here, we reported that Orai1 was overexpressed in gastrointestinal stromal tumor tissues and was positively correlated with a high-risk grade in gastrointestinal stromal tumor patients. Furthermore, upon Orai1 silencing, the functional store-operated Ca 2+ entry in gastrointestinal stromal tumor cells was decreased, indicating that the function of store-operated Ca 2+ entry was mediated by Orai1. Inhibition of Orai1-mediated store-operated Ca 2+ entry by Orai1 silencing or store-operated Ca 2+ entry blockers (SKF-96365 and 2-aminoethyl diphenylborate) induced obvious cell proliferation suppression, cell-cycle distribution, and apoptosis stimulation in GIST-T1 cells. Conversely, Orai1 overexpression increased store-operated Ca 2+ entry and cell proliferation in GIST882 cells. In addition, we found that activation of c-KIT and the extracellular signal–regulated kinase pathway participated in the oncogenic functions of Orai1-mediated store-operated Ca 2+ entry in gastrointestinal stromal tumor cells. These results revealed that Orai1-mediated store-operated Ca 2+ entry is critical for gastrointestinal stromal tumor cell proliferation via c-KIT and ERK signaling pathway activation. Orai1-mediated store-operated Ca 2+ entry plays an oncogenic role and may be a novel prognostic factor and therapeutic target for patients with gastrointestinal stromal tumors.
ISSN:1423-0380
DOI:10.1177/1010428317691426