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Circular RNA CDR1as sponges miR-7-5p to enhance E2F3 stability and promote the growth of nasopharyngeal carcinoma

机译:环状RNA CDR1作为海绵体miR-7-5p增强E2F3稳定性并促进鼻咽癌的生长

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Circular RNA (circRNA) CDR1as plays an important role in the occurrence and development of human tumors. The purpose of this study is to investigate the molecular mechanism of circRNA CDR1as in the development of nasopharyngeal carcinoma (NPC). The mRNA expressions of circRNA CDR1as, miR-7-5p, and E2F3 were detected by qRT-PCR. The effects of circRNA CDR1as, miR-7-5p, and E2F3 on NPC cells were investigated using cell counting kit-8 (CCK8) method, colony formation assay, and representative metabolite assay. The molecular mechanism of circRNA CDR1 in NPC was studied by bioinformatics and luciferase reporter assay. In addition, the biological activity of circRNA CDR1as was also investigated in NPC xenograft tumor mice model. The results showed that the circRNA CDR1as expression was significantly up-regulated in NPC tissues by comparison with non-tumor NPE tissues (p??0.01), suggesting that circRNA CDR1as was associated with poor prognosis in NPC patients. Moreover, circRNA CDR1as could up-regulate E2F3 expression by binding miR-7-5p, and promote the growth and glucose metabolism of NPC cells. Meanwhile, circRNA CDR1as could promote NPC progression through the negative regulation of miR-7-5p in the xenograft tumor model. CircRNA CDR1as promoted the occurrence and development of NPCs by successively up-regulating the expression of miR-7-5p and E2F3, suggesting CircRNA CDR1as as a potential target for the treatment of NPC patients.
机译:环状RNA(circRNA)CDR1as在人类肿瘤的发生和发展中起着重要作用。本研究的目的是研究circRNA CDR1as在鼻咽癌(NPC)发生中的分子机制。通过qRT-PCR检测circRNA CDR1as,miR-7-5p和E2F3的mRNA表达。使用细胞计数试剂盒8(CCK8)方法,集落形成测定和代表性代谢产物测定,研究了circRNA CDR1as,miR-7-5p和E2F3对NPC细胞的作用。通过生物信息学和萤光素酶报告基因检测研究了NPC中circRNA CDR1的分子机制。此外,还在NPC异种移植肿瘤小鼠模型中研究了circRNA CDR1as的生物学活性。结果表明,与非肿瘤的NPE组织相比,NPC组织中circRNA CDR1as的表达显着上调(p 0.01),表明circRNA CDR1as与NPC患者的预后不良有关。此外,circRNA CDR1as可以通过结合miR-7-5p上调E2F3表达,并促进NPC细胞的生长和葡萄糖代谢。同时,circRNA CDR1as可以通过在异种移植肿瘤模型中对miR-7-5p的负调控来促进NPC进程。通过连续上调miR-7-5p和E2F3的表达,CircRNA CDR1as促进了NPC的发生和发展,提示CircRNA CDR1as是治疗NPC的潜在靶标。

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