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首页> 外文期刊>Thoracic cancer. >Circular RNA CirCHIPK3 promotes cell proliferation and invasion of breast cancer by sponging miR ‐ 193a / HMGB1 / PI3K / AKT axis
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Circular RNA CirCHIPK3 promotes cell proliferation and invasion of breast cancer by sponging miR ‐ 193a / HMGB1 / PI3K / AKT axis

机译:圆形RNA circhipk3通过冲水 - 193A / HMGB1 / PI3K / AKT轴促进细胞增殖和侵袭乳腺癌

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BACKGROUND:The aim of this study was to explore the potential mechanism of circular RNA (circRNA) CirCHIPK3 on the malignant proliferation and metastasis of breast cancer (BC).METHODS:Human BC samples and their matched normal adjacent tissues were obtained from 50 patients to assess the expression of CirCHIPK3 and its relationship with BC prognosis. A series of in vitro and in vivo functional experiments were carried out to elucidate the role of CirCHIPK3 in BC progression and its underlying molecular mechanisms. Moreover, the interaction of CirCHIPK3, miR-193a, and HMGB1 was examined using bioinformatics, FISH, RIP, RNA-pull down and luciferase reporter assays. Western blot analysis was performed to examine the expression of HMGB1, p-PI3K, total PI3K, p-AKT, and AKT after si-CirCHIPK3 transfection.RESULTS:Upregulation of CirCHIPK3 was identified in BC, which predicted a worse prognosis in BC patients. Furthermore, it was found that CirCHIPK3 facilitated cell proliferation, migration, and invasion in BC by regulating miR-193a/HMGB1/PI3K/AKT signaling. CirCHIPK3 acted as a sponge for miR-193a to facilitate HMGB1 expression. si-CirCHIPK3 also inhibited tumor growth of BC in nude mice. si-CircCHIPK3 decreased HMGB1/PI3K/AKT signal expression in MDA-MB-231 cells, whereas overexpression of CircCHIPK3 enhanced HMGB1/PI3K/AKT signal.CONCLUSIONS:CirCHIPK3 regulated miR-193a/HMGB1/PI3K/AKT signaling to facilitate BC development and progression, providing a novel therapeutic target for BC.? 2020 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd.
机译:背景:本研究的目的是探讨圆形RNA(Circrna)Circhipk3对乳腺癌恶性增殖和转移的潜在机制(BC)。方法:人类BC样品和其匹配的正常相邻组织是从50例患者获得评估Circhipk3的表达及其与BC预后的关系。进行了一系列体外和体内功能实验,以阐明Circhipk3在BC进展中的作用及其潜在的分子机制。此外,使用生物信息学,鱼类,RIP,RNA拉管和荧光素酶报告器测定来检查CiRChipk3,miR-193a和HMGB1的相互作用。进行Western印迹分析以检查Si-circhipk3转染后HMGB1,P-PI3K,总Pi3K,P-AKT和AKT的表达,CO-Chipk3转染后的表达:在BC中鉴定了Circhipk3的上调,预测了BC患者的预后更糟。此外,发现通过调节miR-193a / hmgb1 / pi3k / akt信号传导,Circhipk3促进细胞增殖,迁移和侵袭。 Circhipk3充当MIR-193A的海绵,以促进HMGB1表达。 Si-circhipk3还抑制了裸鼠中BC的肿瘤生长。 Si-CircChipk3减少了MDA-MB-231细胞中HMGB1 / PI3K / AKT信号表达,而CircChipk3的过度表达增强了HMGB1 / PI3K / AKT信号。结论:Circhipk3调节MiR-193A / HMGB1 / PI3K / AKT信号,以促进BC开发和进展,为BC提供新的治疗目标。 2020作者。中国肺部肿瘤集团和约翰瓦里和儿子澳大利亚发表的胸癌

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