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首页> 外文期刊>Cell death & disease. >The long non-coding RNA FOXD2-AS1 promotes bladder cancer progression and recurrence through a positive feedback loop with Akt and E2F1
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The long non-coding RNA FOXD2-AS1 promotes bladder cancer progression and recurrence through a positive feedback loop with Akt and E2F1

机译:长期非编码RNA FOXD2-AS1通过AKT和E2F1的正反馈环促进膀胱癌进展和复发性

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Long non-coding RNAs (lncRNAs) have been identified as significant regulators in cancer progression. Positive feedback loops between lncRNAs and transcription factors have attracted increasing attention. Akt pathway plays a crucial role in bladder cancer growth and recurrence. In the present study, we demonstrate a novel regulatory pattern involving FOXD2-AS1, Akt, and E2F1. FOXD2-AS1 is highly expressed in bladder cancer and is associated with tumor stage, recurrence, and poor prognosis. Further experiments showed that FOXD2-AS1 promotes bladder cancer cell proliferation, migration, and invasion in vitro and in vivo. Microarray analysis demonstrated that FOXD2-AS1 negatively regulates the expression of Tribbles pseudokinase 3 (TRIB3), a negative regulator of Akt. Mechanistically, FOXD2-AS1 forms an RNA-DNA complex with the promoter of TRIB3, the transcriptional activity of which is subsequently repressed, and leads to the activation of Akt, which further increases the expression of E2F1, a vital transcription factor involved in the G/S transition. Interestingly, E2F1 could bind to the FOXD2-AS1 promoter region and subsequently enhance its transcriptional activity, indicating that FOXD2-AS1/Akt/E2F1 forms a feedback loop. In summary, this regulatory pattern of positive feedback may be a novel target for the treatment of bladder cancer and FOXD2-AS1 has the potential to be a new recurrence predictor.
机译:长期未编码RNA(LNCRNA)已被鉴定为癌症进展中的重要调节剂。 LNCRNA和转录因子之间的正反馈循环引起了越来越多的关注。 Akt途径在膀胱癌生长和复发中起着至关重要的作用。在本研究中,我们展示了涉及Foxd2-AS1,AKT和E2F1的新型调节模式。 Foxd2-AS1在膀胱癌中高度表达,与肿瘤阶段,复发性和预后不良有关。进一步的实验表明,Foxd2-AS1促进膀胱癌细胞增殖,迁移和体内侵袭。微阵列分析证明Foxd2-AS1负调节Troughts伪转子酶3(TRED3)的表达,AKT的负调节剂。机械地,FOXD2-AS1与TRED3的启动子形成RNA-DNA络合物,随后将其转录活性抑制,并导致AKT的激活,这进一步增加了E2F1的表达,这是G的重要转录因子。 / s过渡。有趣的是,E2F1可以与FoxD2-AS1启动子区结合,随后增强其转录活性,表明FoxD2-AS1 / AKT / E2F1形成反馈回路。总之,这种阳性反馈的调节模式可以是膀胱癌和Foxd2-AS1的治疗的新靶标,有可能成为一种新的复发预测因子。

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