| Journal of Translational Medicine | |
| CD24 associates with EGFR and supports EGF/EGFR signaling via RhoA in gastric cancer cells | |
| Research | |
| Wenjie Deng1  Jun Du1  Yujie Zhang2  Luo Gu2  Jie Cui3  Jing Dong4  Xiaojie Li5  Biao Duan5  Jianchao Zheng5  | |
| [1] Cancer Center, Nanjing Medical University, 140 Hanzhong Road, 210029, Nanjing, Jiangsu, China;Department of Physiology, Nanjing Medical University, 210029, Nanjing, Jiangsu, China;Cancer Center, Nanjing Medical University, 140 Hanzhong Road, 210029, Nanjing, Jiangsu, China;Department of Physiology, Nanjing Medical University, 210029, Nanjing, Jiangsu, China;Department of Biochemistry and Molecular Biology, Nanjing Medical University, 210029, Nanjing, Jiangsu, China;Department of Biochemistry and Molecular Biology, Nanjing Medical University, 210029, Nanjing, Jiangsu, China;Department of Biochemistry and Molecular Biology, Nanjing Medical University, 210029, Nanjing, Jiangsu, China;Epidemiology and Biostatistics and Ministry of Education (MOE) Key Laboratory for Modern Toxicology, Nanjing Medical University, 210029, Nanjing, Jiangsu, China;Department of Physiology, Nanjing Medical University, 210029, Nanjing, Jiangsu, China; | |
| 关键词: CD24; EGFR; RhoA; Gastric cancer; | |
| DOI : 10.1186/s12967-016-0787-y | |
| received in 2015-03-23, accepted in 2016-01-18, 发布年份 2016 | |
| 来源: Springer | |
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【 摘 要 】
BackgroundCD24, a mucin-like membrane glycoprotein, plays a critical role in carcinogenesis, but its role in human gastric cancer and the underlying mechanism remains undefined.MethodsThe contents of CD24 and epidermal growth factor receptor (EGFR) in gastric cancer cells (SGC-7901 and BGC-823) and non-malignant gastric epithelial cells (GES-1) were evaluated by Western blotting assay. Cellular EGFR staining was examined by immunofluorescence assay. Cell migration rate was measured by wound healing assay. The effects of depletion/overexperssion of CD24 on EGFR expression and activation of EGF/EGFR singaling pathways were evaluated by immunofluorescence, qPCR, Western blotting and flow cytometry techniques. RhoA activity was assessed by pulldown assay. CD24 and EGFR expression patterns in human gastric tumor samples were also investigated by immunohistochemistry staining.ResultsCD24 was overexpressed in human gastric cancer cells. Ectopic expression of CD24 in gastric epithelial cells augmented the expression of EGFR, while knockdown of CD24 in gastric cancer cells decreased the level of EGFR and cell migration velocity. To further explore the mechanisms, we investigated the effect of CD24 expression on EGF/EGFR signaling. We noticed that this effect of CD24 on EGFR expression was dependent on promoting EGFR internalization and degradation. Lower ERK and Akt phosphorylations in response to EGF stimulation were observed in CD24-depleted cells. In addition, we noticed that the effect of CD24 on EGFR stability was mediated by RhoA activity in SGC-7901 gastric cancer cells. Analysis of gastric cancer specimens revealed a positive correlation between CD24 and EGFR levels and an association between CD24 expression and worse prognosis.ConclusionThus, these findings suggest for the first time that CD24 regulates EGFR signaling by inhibiting EGFR internalization and degradation in a RhoA-dependent manner in gastric cancer cells.
【 授权许可】
CC BY
© Deng et al. 2016
【 预 览 】
| Files | Size | Format | View |
|---|---|---|---|
| RO202311100525074ZK.pdf | 2238KB |
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