Involvement of acid-sensing ion channel 1a in gastric carcinoma cell migration and invasion. (23rd March 2018)

• Record Type: Journal Article
• Authors: Chen, Xin; Sun, Xue; Wang, Zhe; Zhou, Xiaojun; Xu, Lu; Li, Feng'e; Zhang, Xingding; Pan, Ji'an; Qi, Lin; Qian, Haixin; Mao, Zhongqi
• Is Part Of: Acta biochimica et biophysica Sinica. Volume 50:Number 5(2018:May)
• Page Start: 440
• Page End: 446
• Publication Date: 2018-03-23
• Subjects: acid-sensing ion channel 1a -- gastric carcinoma -- migration -- invasion; Biochemistry -- Periodicals; Biophysics -- Periodicals; 572.05
• DOI: 10.1093/abbs/gmy026
• Languages: English
• ISSNs: 1672-9145

Abstract

Abstract: Acidic microenvironment, particularly acid-sensing ion channel 1a (ASIC1a), has been reported to promote carcinoma cell proliferation as well as migration. In this study, we explored the effect of ASIC1a on migration and invasion of gastric carcinoma (GC). ASIC1a expression levels were examined in paired GC and adjacent normal tissues from 16 patients by immunohistochemistry. Reverse transcription real-time PCR and immunoblotting were conducted to assess the ASIC1a expression levels in the GC cell line AGS after transfection with ASIC1a small hairpin RNA (shRNA). Wound healing and transwell invasion assays were utilized to detect metastasis and invasion following ASIC1a silencing. Tumor formation was used to detect the role of ASIC1a in tumorigenicity in vivo . It was found that ASIC1a expression level was significantly higher in GC tissues showing postoperative metastasis compared with non-metastasis and non-tumor tissues. Moreover, silencing of ASIC1a with shRNA significantly down-regulated ASIC1a expression and reduced GC cell migration and invasion. A moderately acidic extracellular environment inhibited GC cell viability. Furthermore, ASIC1a shRNA caused inhibition of tumorigenicity in vivo . Our study is the first report of attenuating the malignant phenotype of GC in vitro and in vivo by suppressing ASIC1a, and suggests a novel approach to study the relationship between ASICs and GC cell migration and invasion.