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首页> 外文期刊>Biochemistry and Cell Biology >circ-NOTCH1 acts as a sponge of miR-637 and affects the expression of its target gene Apelin to regulate gastric cancer cell growth
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circ-NOTCH1 acts as a sponge of miR-637 and affects the expression of its target gene Apelin to regulate gastric cancer cell growth

机译:循环NOTCH1用作miR-637的海绵,并影响其靶基因脂素的表达来调节胃癌细胞生长

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Gastric cancer (GC) is a major cause of cancer-related deaths worldwide, and has a low survival rate, low cure rate, high recurrence rate, and poor prognosis. Recent studies have indicated that circular RNAs (circRNAs) have important functions in the occurrence and progression of GC. Studies on circ-NOTCH1, which was shown to be highly expressed in GC, have indicated that miR-637 binds to circ-NOTCH1 at multiple sites, and a dual-luciferase reporter gene assay further confirmed that miR-637 indeed targeted circ-NOTCH1 and Apelin. Circ-NOTCH1 and Apelin are highly expressed in GC cells and tissues, whereas the expression of miR-637 is reduced. Circ-NOTCH1 and miR-637 do not regulate each other’s expression levels, but circ-NOTCH1significantly upregulates the expression of the miR-637 target gene Apelin, whereas miR-637 inhibites the expression of Apelin. Examination of GC cells showed that circ-NOTCH1 enhances cell proliferation and invasiveness, and reduces cell apoptosis; these effects were reversed by miR-637, which could terminate the above effects of circ-NOTCH1. When co-transfected with the circ-NOTCH1 overexpression plasmid and Apelin siRNAs, there were no obvious changes to the levels of cell proliferation, apoptosis, or invasiveness. Therefore, in GC cells, circ-NOTCH1 inhibits the transcriptional activity of miR-637, thereby upregulating the expression of its target gene Apelin and regulating cell proliferation, apoptosis, and invasiveness. This finding provides more experimental evidence for the function of circRNA in GC.
机译:胃癌(GC)是全世界癌症相关死亡的主要原因,生存率低,治愈率低,复发率高,预后差。最近的研究表明,圆形RNA(Circrnas)在GC的发生和进展中具有重要功能。在GC中显示出高度表达的循环Notch1的研究表明,MIR-637在多个位点结合循环NOTCH1,并且双荧光素酶报告基因测定进一步证实MIR-637实际上是靶向循环NOTCH1和阿贝林。循环Notch1和Apelin在GC细胞和组织中高度表达,而MiR-637的表达减少。 Circ-Notch1和MiR-637不调节彼此的表达水平,但是循环毫无张突显上调MiR-637靶基因阿皮肽的表达,而MiR-637抑制阿比松的表达。对GC细胞的检查表明,循环诺奇1增强细胞增殖和侵袭性,降低细胞凋亡; MiR-637逆转了这些效果,其可以终止上述电路Notch1的效果。当用CiRC-Notch1过表达质粒和Apelin siRNA共转染时,对细胞增殖,细胞凋亡或侵袭性的水平没有明显的变化。因此,在GC细胞中,循环诺奇1抑制miR-637的转录活性,从而提高其靶基因素和调节细胞增殖,细胞凋亡和侵袭性的表达。该发现为GC中的Circrna功能提供了更多的实验证据。

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