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环状锌指蛋白SCAN域包含蛋白1(Circ-ZKSCAN1)通过靶向微小RNA-330-5p(miR-330-5p)调节FAM83A表达并使丝裂原活化蛋白激酶(MAPK)信号失活,从而促进非小细胞肺癌进展。

Circ-ZKSCAN1 regulates FAM83A expression and inactivates MAPK signaling by targeting miR-330-5p to promote non-small cell lung cancer progression.

作者信息

Wang Yuanyong, Xu Rongjian, Zhang Dongyang, Lu Tong, Yu Wanpeng, Wo Yang, Liu Ao, Sui Tianyi, Cui Jian, Qin Yi, Dong Yanting, Leng Xiaoliang, Kong Dezhi, Du Wenxing, Huang Zhangfeng, Su Wenhao, Yuan Tianxiang, Sun Xiao, Wang Jianxun, Jiao Wenjie

机构信息

Department of Thoracic Surgery, Affiliated Hospital of Qingdao University, Qingdao 266000, China.

Center for Regenerative Medicine, Institute for Translational Medicine, College of Medicine, Qingdao University, Qingdao 266000, China.

出版信息

Transl Lung Cancer Res. 2019 Dec;8(6):862-875. doi: 10.21037/tlcr.2019.11.04.

Abstract

BACKGROUND

Circular RNAs (circRNAs) belong to a new type of endogenous non-coding RNA and plays a key role in carcinogenesis. Circ-ZKSCAN1 (hsa_circ_0001727) has been proven to be a tumor-dependent circRNA. However, its role in non-small cell lung cancer (NSCLC) has been underreported.

METHODS

The expression patterns of circ-ZKSCAN1 were determined using qRT-PCR in NSCLC samples and cell lines. Cell proliferation was examined utilizing the CCK-8 assay. Cell migration and invasion were evaluated using the Transwell assay. The combination of circ-ZKSCAN1 and miR-330-5p in NSCLC cells was analyzed by RNA pull-down and luciferase reporter assay. We used the bioinformatics software circbank, CircInteractome, TargetScan and Miranda to predict circRNA-miRNA and miRNA-mRNA interactions.

RESULTS

Our results showed that circ-ZKSCAN1 was significantly up-regulated in NSCLC, closely related to malignant characteristics and poor prognosis, and clinically related to tumor size and clinical stage. Subsequent experiments showed that circ-ZKSCAN1 could inhibit the growth of NSCLC cells in vitro and in vivo. Importantly, circ-ZKSCAN1 can act as a sponge of carcinogenic miR-330-5p to increase the expression of FAM83A, resulting in the inhibition of MAPK signal transduction pathway, thus promoting the progress of NSCLC. Interestingly, the increase in FAM83A expression caused by circ-ZKSCAN1 overexpression could in turn promote the expression of circ-ZKSCAN1.

CONCLUSIONS

Circ-ZKSCAN1 is a key positive regulator of NSCLC, and clarifies the potential molecular mechanism of the new circ-ZKSCAN1/miR-330-5p/FAM83A feedback loop in promoting the progress of NSCLC.

摘要

背景

环状RNA(circRNAs)属于一类新型内源性非编码RNA,在肿瘤发生过程中起关键作用。Circ-ZKSCAN1(hsa_circ_0001727)已被证明是一种肿瘤相关的环状RNA。然而,其在非小细胞肺癌(NSCLC)中的作用报道较少。

方法

采用qRT-PCR检测NSCLC样本和细胞系中circ-ZKSCAN1的表达模式。利用CCK-8法检测细胞增殖。采用Transwell法评估细胞迁移和侵袭能力。通过RNA下拉和荧光素酶报告基因检测分析NSCLC细胞中circ-ZKSCAN1与miR-330-5p的结合情况。我们使用生物信息学软件circbank、CircInteractome、TargetScan和Miranda预测circRNA-miRNA和miRNA-mRNA相互作用。

结果

我们的结果表明,circ-ZKSCAN1在NSCLC中显著上调,与恶性特征和不良预后密切相关,且在临床上与肿瘤大小和临床分期相关。后续实验表明,circ-ZKSCAN1在体外和体内均可抑制NSCLC细胞的生长。重要的是,circ-ZKSCAN1可作为致癌性miR-330-5p的海绵,增加FAM83A的表达,导致MAPK信号转导通路受到抑制,从而促进NSCLC的进展。有趣的是,circ-ZKSCAN1过表达引起的FAM83A表达增加反过来又可促进circ-ZKSCAN1的表达。

结论

Circ-ZKSCAN1是NSCLC的关键正调控因子,并阐明了新的circ-ZKSCAN1/miR-330-5p/FAM83A反馈环在促进NSCLC进展中的潜在分子机制。

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