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首页> 外文期刊>Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function >CircFOXO3 functions as a molecular sponge for miR-143-3p to promote the progression of gastric carcinoma via upregulating USP44
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CircFOXO3 functions as a molecular sponge for miR-143-3p to promote the progression of gastric carcinoma via upregulating USP44

机译:循环氧化丝用作MiR-143-3P的分子海绵,通过上调USP44来促进胃癌的进展

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摘要

Gastric carcinoma (GC) ranks fifth in terms of cancer morbidity and third in cancer-related death worldwide and imposes enormous health and economic burdens. The molecular mechanisms underlying GC formation and progression remain unclear. Our aim was to identify the involvement of circular RNA circFOXO3 in GC, and to determine the underlying mechanisms. In this study, we revealed a stimulatory role of circular RNA circFOXO3 in tumor growth in vivo. CircFOXO3 enhanced GC cell proliferation and migration in vitro and promoted tumor growth of GC cells in vivo. Bioinformatic analysis revealed that circFOXO3 might regulate USP44 expression by specifically binding to microRNA (miR)-143-3p. Existence of circFOXO3-miR-143-3p-USP44 axis in GC cells was confirmed by RNA-binding protein immunoprecipitation, luciferase reporter assay, and an RNA pull-down experiments. All the data indicate that circFOXO3 promotes GC cell proliferation and migration by upregulating USP44 expression via targeting of miR-143-3p.
机译:胃癌(GC)在全世界癌症发病率和第三个在癌症相关死亡方面排名第五,并造成了巨大的健康和经济负担。 GC形成和进展的分子机制仍不清楚。我们的目的是识别循环RNA循环循环赛中GC的参与,并确定潜在机制。在这项研究中,我们揭示了圆形RNA循环循环循环在体内肿瘤生长中的刺激作用。循环氧化烃增强型GC细胞增殖和体外迁移,促进体内GC细胞的肿瘤生长。生物信息分析表明,循环氧化烃可以通过特异性结合MicroRNA(miR)-143-3p来调节USP44表达。通过RNA结合蛋白免疫沉淀,荧光素酶报告试验和RNA下拉实验证实了GC细胞中循环氧化物3-MIR-143-3P-USP44轴的存在性。所有数据表明,循环氟肟3通过靶向MIR-143-3P来提高USP44表达来促进GC细胞增殖和迁移。

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