首页> 外文期刊>Journal of clinical laboratory analysis. >CircRNA WHSC1 promotes non-small cell lung cancer progression via sponging microRNA-296-3p and up-regulating expression of AKT serine/threonine kinase 3
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CircRNA WHSC1 promotes non-small cell lung cancer progression via sponging microRNA-296-3p and up-regulating expression of AKT serine/threonine kinase 3

机译:Circrna Whsc1通过海绵MicroRNA-296-3P提高非小细胞肺癌进展和AKT丝氨酸/苏氨酸激酶3的上调表达

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Background Lung cancer is the most commonly diagnosed cancer and leading cause of cancer death, with 80%–85% of non-small cell lung cancer (NSCLC). Circular RNAs (circRNAs) have been shown to be promising early diagnostic and therapeutic molecular biomarkers for NSCLC. However, biological role and regulatory mechanism of circRNA WHSC1 (circWHSC1) in NSCLC are unknown. Therefore, we aim to explore the function and mechanism of circWHSC1 in NSCLC oncogenesis and progression. Methods qRT-PCR was used for circWHSC1 level evaluation; Kaplan-Meier was used for survival analysis; bioinformatics, dual-luciferase activity, and RNA pull-down were used for evaluating competing endogenous RNA (ceRNA) network; cell viability, colony formation, apoptosis, migration, and invasion were used for cell function analysis; function gain and loss with rescue experiments were used for exploring mechanism of circWHSC1 in NSCLC development. Results Significantly up-regulated circWHSC1 and down-regulated microRNA-296-3p (miR-296-3p) were identified in NSCLC tissues and cells. Up-regulated circWHSC1 was associated with poor prognosis in NSCLC patients. MiR-296-3p was sponged by circWHSC1, and AKT serine/threonine kinase 3 (AKT3) was target of miR-296-3p; meanwhile, miR-296-3p over-expression significantly down-regulated AKT3 expression, and co-transfecting anti-miR-296-3p rescued circWHSC1?silence caused AKT3 down-regulation. CircWHSC1?silence significantly inhibited colony formation, viability, invasion, and migration, while increased NSCLC cell apoptosis, which were partially rescued by anti-miR-296-3p. Conclusion CircWHSC1 is an independent indicator of poor prognosis in NSCLC patients, and functions as a ceRNA of miR-296-3p to up-regulate AKT3, consequently promotes NSCLC cell growth and metastasis. Targeting circWHSC1?might be a prospective strategy for diagnosis, therapeutics, and prognosis of NSCLC.
机译:背景技术肺癌是癌症最常见的癌症和主要原因,80%-85%的非小细胞肺癌(NSCLC)。圆形RNA(CircRNA)已被证明是NSCLC的早期诊断和治疗分子生物标志物。然而,NSCLC中Circrna Whsc1(CircWhsc1)的生物作用和调节机制是未知的。因此,我们的目标是探讨NSCLC蜂癌生成和进展中Circwhsc1的功能和机制。方法QRT-PCR用于CircWhSC1水平评价; Kaplan-Meier用于存活分析;生物信息学,双荧光素酶活性和RNA下拉用于评估竞争内源性RNA(CERNA)网络;细胞活力,菌落形成,细胞凋亡,迁移和侵袭用于细胞功能分析;救援实验的功能增益和损失用于探索NSCLC开发中的CircWhsc1的机制。结果在NSCLC组织和细胞中鉴定出显着上调的昼夜昼夜昼夜昼夜昼夜循环〜296-3p(miR-296-3p)。上调的昼夜循环株式会有问题与NSCLC患者的预后差有关。 MiR-296-3P由CircWhSC1和AKT丝氨酸/苏氨酸激酶3(AKT3)是miR-296-3p的靶标;同时,MIR-296-3P过表达显着下调AKT3表达,并共转染抗MIR-296-3P救出了CircWhSC1?沉默导致AKT3下调。 Circwhsc1?沉默显着抑制菌落形成,活力,侵袭和迁移,同时增加了NSCLC细胞凋亡,其部分通过抗miR-296-3p抵抗。结论CircWhsc1是NSCLC患者预后不良的独立指标,并作为MIR-296-3P的CERNA,因此促进了NSCLC细胞生长和转移。瞄准CIRCWHSC1?可能是NSCLC诊断,治疗和预后的前瞻性策略。

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