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Downregulation of Lnc-OC1 attenuates the pathogenesis of polycystic ovary syndrome

机译:LNC-OC1的下调衰减多囊卵巢综合征的发病机制

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Long non-coding RNAs (lncRNAs) play a vital role in the progression of many human diseases. The aim of this study is to explore the relationship between 1ncRNA-ovarian cancer associated 1 (Lnc-OC1) and PCOS. In this study, we found that Lnc-OC1 was significantly higher in PCOS granulosa cells (GCs) compared to non-PCOS GCs. Lnc-OC1 knockdown inhibited cell viability and promoted cell apoptosis, expression of aromatase mRNA and production of estradiol in KGN cells. In PCOS mice, Lnc-OC1 promoted the serum insulin release, production of angiogenesis-related factors and I kappa B alpha phosphorylation, which could be partially restored by Lnc-OC1 shRNA. These results suggest that Lnc-OC1 plays an important part in the pathogenesis of PCOS.
机译:长期非编码RNA(LNCRNA)在许多人类疾病的进展中起着至关重要的作用。 本研究的目的是探讨1ncra-卵巢癌相关的1(LNC-OC1)和PCO之间的关系。 在本研究中,与非PCOS GCS相比,我们发现PCOS颗粒细胞(GCS)中的LNC-OC1显着较高。 LNC-OC1敲低抑制细胞活力和促进细胞凋亡,芳香酶mRNA的表达和在KGN细胞中产生雌二醇。 在PCOS小鼠中,LNC-OC1促进了血清胰岛素释放,产生了血管生成相关因子和I KappaBα磷酸化,其可以通过LNC-OC1 ShRNA部分恢复。 这些结果表明,LNC-OC1在PCOS的发病机制中起重要作用。

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