首页> 外文期刊>Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function >Circ-ATP8A2 promotes cell proliferation and invasion as a ceRNA to target EGFR by sponging miR-433 in cervical cancer
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Circ-ATP8A2 promotes cell proliferation and invasion as a ceRNA to target EGFR by sponging miR-433 in cervical cancer

机译:循环ATP8A2促进细胞增殖和侵袭作为CERNA以宫颈癌的miR-433靶向EGFR

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摘要

Cervical cancer (CC), a common gynecological carcinoma, is a serious threat to women's health. The dysregulation of circular RNAs (circRNAs) is associated with the pathogenesis of cervical cancer. Therefore, we explored the role of circ-ATP8A2 in CC cell development and progression. Circ-ATP8A2 profiles in CC specimens and cells were detected using real-time PCR. In addition, cell counting kit-8 (CCK-8), acridine orange/ethidium bromide (AO/EB), flow cytometric, and Transwell experiments were carried out on HeLa and SW756 cells to determine cell proliferation, apoptosis, migration and invasion. Furthermore, the mechanism of circ-ATP8A2 was explored by dual-luciferase reporter system. Circ-ATP8A2 was significantly enhanced in CC specimens and cells. Knockdown of circ-ATP8A2 inhibited cell proliferation, migratory and invasive capacities and increased apoptotic cells. Ectopically expressed circ-ATP8A2 induced the opposite effects. For the mechanism exploration, circATP8A2 sponges miR-433 to release its suppression on epidermal growth factor receptor (EGFR) expression at post-transcriptional level. What's more, circ-ATP8A2 could promote cell progression by miR-433/EGFR axis in CC cells. Collectively, this work might offer a potential treatment target for CC.
机译:宫颈癌(CC)是一种常见的妇科癌,对女性健康有严重威胁。圆形RNA(Circrnas)的失调与宫颈癌的发病机制有关。因此,我们探讨了CIC-ATP8A2在CC细胞开发和进展中的作用。使用实时PCR检测CC样本和细胞中的循环ATP8A2型材。此外,在Hela和SW756细胞上进行细胞计数试剂盒-8(CCK-8),吖啶橙/乙锭(AO / EB),流式细胞术和Transwell实验,以确定细胞增殖,细胞凋亡,迁移和侵袭。此外,通过双荧光素酶报告系统探索了循环ATP8A2的机制。 CC样本和细胞中CIRP-ATP8A2显着增强。循环循环循环循环抑制抑制细胞增殖,迁移和侵袭性和增加的凋亡细胞。异位表达的循环循环诱导效应相反。对于机制勘探,Circatp8a2海绵MiR-433释放其在转录后水平的表皮生长因子受体(EGFR)表达上的抑制。更重要的是,CIC-ATP8A2可以通过CC细胞中的miR-433 / EGFR轴促进细胞进展。统称,这项工作可能为CC提供潜在的治疗目标。

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