期刊文献+
共找到3篇文章
< 1 >
每页显示 20 50 100
UCK2 promotes the proliferation,migration,and invasion of trophoblast cells in preeclampsia by activating the STAT3 pathway
1
作者 WEI XIA NING YANG +4 位作者 XIAOYAN FENG TING XIN YONGLE JING YUMING LI CHENGZHI LU 《BIOCELL》 SCIE 2023年第4期837-847,共11页
Background:Preeclampsia(PE),characterized by hypertension and proteinuria,leads to serious maternal and infant complications.Uridine-cytidine kinase 2(UCK2)belongs to the UCK family,a class of enzymes that catalyzes t... Background:Preeclampsia(PE),characterized by hypertension and proteinuria,leads to serious maternal and infant complications.Uridine-cytidine kinase 2(UCK2)belongs to the UCK family,a class of enzymes that catalyzes the conversion of uridine and cytidine to monophosphate form.However,the role of UCK2 in PE has not been reported.Methods:The expression of UCK2 was detected in the placenta of PE patients and N(ω)-nitro-L-arginine methyl esterinduced PE mouse model.Through forced up-regulation or down-regulation of UCK2 in vitro,we examined the effects of UCK2 on the proliferation,apoptosis,migration,and invasion of trophoblast cells.Stattic,the inhibitor of STAT3 pathway,was used to investigate whether the STAT3 pathway mediates the biological function of UCK2 in trophoblast cells.Results:The present study found that UCK2 showed low expression in the placenta of PE patients and PE mouse model.MTT(3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide)and flow cytometry assays verified that up-regulation of UCK2 promoted the proliferation of trophoblast cells,while the silence of UCK2 suppressed cell proliferation.Besides,flow cytometry and TdT-mediated dUTP Nick-End Labeling assays demonstrated that knockdown of UCK2 resulted in apoptosis of trophoblast cells.The wound healing and transwell assays showed that the migration and invasion activities of the trophoblast cells were facilitated by the overexpression of UCK2 and were blocked by the silence of UCK2.Furthermore,the expression of phosphorylated STAT3 was increased with the upregulation of UCK2 and decreased with the inhibition of UCK2.When the STAT3 pathway was blocked by its inhibitor stattic,the promotion effects of UCK2 on trophoblast cells were suppressed.Conclusion:UCK2 promotes the proliferation,migration,and invasion of trophoblast cells,and these effects may be partly mediated by the activation of the STAT3 pathway. 展开更多
关键词 uck2 PREECLAMPSIA STAT3 TROPHOBLAST INVASION
下载PDF
基于TCGA数据库分析肝细胞癌组织UCK2、PRIM1和DNTM1基因水平对患者预后的影响 被引量:1
2
作者 赵艺 卢秉久 《实用肝脏病杂志》 CAS 2021年第5期729-732,共4页
目的通过分析TCGA数据库肝细胞癌(HCC)组织基因组数据,分析差异基因,寻找影响肝癌患者预后的分子标志物。方法搜索癌症基因图谱(TCGA)数据库,查找HCC组织差异基因及临床和病理学资料,进行基因筛选和生存分析。根据差异基因水平,以fdr=0... 目的通过分析TCGA数据库肝细胞癌(HCC)组织基因组数据,分析差异基因,寻找影响肝癌患者预后的分子标志物。方法搜索癌症基因图谱(TCGA)数据库,查找HCC组织差异基因及临床和病理学资料,进行基因筛选和生存分析。根据差异基因水平,以fdr=0.05和lgFC=1为筛选依据,绘制生存曲线,选择基因集“c2.cp.kegg.v6.2.symbols.gmt”行KEGG富集分析。结果在TCGA-LIHC数据库,收集374例HCC组织和50例癌旁组织所对应的临床和病理学参数;高风险组HCC患者总体生存率显著低于低风险组患者;研究筛选出具有显著水平性基因DNTM1、PRIM1和UCK2,进行GSEA富集分析,GSEA显示了许多显著丰富的信号通路,进一步证明了上述基因与HCC发生及与患者预后的显著性关系,从而揭示了HCC组织DNTM1、PRIM1和UCK2基因水平对生存有显著性影响。结论通过TCGA数据库筛选和验证,发现HCC患者癌组织UCK2、PRIM1和DNTM1基因水平显著上调,而CYP2C9基因显著下调,它们可以作为肝癌的分子标志物而指导临床,判断预后。 展开更多
关键词 肝细胞癌 TCGA数据库 差异基因 COX回归模型 uck2 PRIM1 DNTM1
下载PDF
miR-432-5p靶向UCK2调控乳腺癌细胞MCF-7凋亡的研究 被引量:2
3
作者 梁磊 黄飞 曹芳丽 《中国现代普通外科进展》 CAS 2021年第7期518-521,526,共5页
目的 :探讨miR-432-5p调控乳腺癌细胞MCF-7凋亡的分子机制。方法 :过表达或敲低miR-432-5p后,检测乳腺癌细胞MCF-7的凋亡水平。敲低miR-432-5p后,检测miRDB数据库在线分析的靶标的mRNA水平。通过荧光素酶报告系统检测miRNA是否与潜在靶... 目的 :探讨miR-432-5p调控乳腺癌细胞MCF-7凋亡的分子机制。方法 :过表达或敲低miR-432-5p后,检测乳腺癌细胞MCF-7的凋亡水平。敲低miR-432-5p后,检测miRDB数据库在线分析的靶标的mRNA水平。通过荧光素酶报告系统检测miRNA是否与潜在靶标直接结合。过表达或敲低靶标后,分析乳腺癌细胞MCF-7的凋亡水平。结果:过表达miR-432-5p后,乳腺癌细胞MCF-7的凋亡上升(P<0.05);敲低miR-432-5p后,乳腺癌细胞MCF-7的凋亡下降(P<0.05)。miRDB在线分析发现miR-432-5p潜在靶向COL4A5、E2F3、ADAR、UCK2、KRTAP19-6、UTP-23、BACE1、EMX2、WDFY3、ZNF621。过表达miR-432-5p后,乳腺癌细胞MCF-7中UCK2的mRNA水平下降(P<0.05);敲低miR-432-5p后,乳腺癌细胞MCF-7中UCK2的mRNA水平上升(P<0.05)。荧光素酶报告实验发现miR-432-5p靶向UCK2的3端非编码区。过表达UCK2后,乳腺癌细胞MCF-7的凋亡水平下降(P<0.05);敲低UCK2后,乳腺癌细胞MCF-7的凋亡水平上升(P<0.05)。同时敲低miR-432-5p和UCK2后,乳腺癌细胞MCF-7的凋亡水平无显著变化(P>0.05);同时过表达miR-432-5p和UCK2后,乳腺癌细胞MCF-7的凋亡水平无显著变化(P>0.05)。结论 :miR-432-5p通过靶向UCK2的3端非编码区,降低了UCK2的表达水平,随后促进了乳腺癌细胞MCF-7的凋亡。 展开更多
关键词 miR-432-5p uck2 乳腺癌 MCF-7 凋亡
下载PDF
上一页 1 下一页 到第
使用帮助 返回顶部