多嘧啶结合蛋白
癌症研究
生物
转移
基因敲除
RNA结合蛋白
癌基因
癌症
分子生物学
信使核糖核酸
细胞周期
细胞培养
遗传学
基因
作者
Xiaolin Wang,Ce Liang,Shimin Wang,Qiang Ma,Xiaojuan Pan,Ai Ran,Changhong Qin,Bo Huang,Feifei Yang,Yuying Liu,Yuying Zhang,Junwu Ren,Hao Ning,Haiping Li,Yan Jiang,Bin Xiao
出处
期刊:Cells
[Multidisciplinary Digital Publishing Institute]
日期:2024-01-12
卷期号:13 (2): 140-140
被引量:12
标识
DOI:10.3390/cells13020140
摘要
Gastric cancer (GC) is the most common type of malignant tumor within the gastrointestinal tract, and GC metastasis is associated with poor prognosis. Polypyrimidine tract binding protein 1 (PTBP1) is an RNA-binding protein implicated in various types of tumor development and metastasis. However, the role of PTBP1 in GC metastasis remains elusive. In this study, we verified that PTBP1 was upregulated in GC tissues and cell lines, and higher PTBP1 level was associated with poorer prognosis. It was shown that PTBP1 knockdown in vitro inhibited GC cell migration, whereas PTBP1 overexpression promoted the migration of GC cells. In vivo, the knockdown of PTBP1 notably reduced both the size and occurrence of metastatic nodules in a nude mice liver metastasis model. We identified phosphoglycerate kinase 1 (PGK1) as a downstream target of PTBP1 and found that PTBP1 increased the stability of PGK1 by directly binding to its mRNA. Furthermore, the PGK1/SNAIL axis could be required for PTBP1’s function in the promotion of GC cell migration. These discoveries suggest that PTBP1 could be a promising therapeutic target for GC.
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