Hsa_circ_0109320 Serves as a Novel Circular RNA Biomarker in Non-small Cell Lung Cancer by Promoting Metastasis.

IF 2.4 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Xiaoyan Guo, Hongyan Yu, Xiansheng Wang, Shifeng Zhao, Chunyan Wang, Shuai Wang
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Abstract

Non-small cell lung cancer (NSCLC), including squamous cell carcinoma and adenocarcinoma, ranks among the top 10 cancers worldwide in terms of prevalence and mortality. NSCLC, a highly malignant tumor, exhibits distant invasion and migration as well as an unfavorable prognosis. As an innovative circular RNA, hsa _circ_0109320 (circ_0109320) has been recognized as a promising cancer modulator. However, our understanding of the influence of circ_0109320 in NSCLC remains insufficient. Our research explored the clinical significance and effects of circ_0109320 on oncogenic non-small cell lung cancer (NSCLC) phenotypes. Microarray analysis and qPCR indicated that circ_0109320 expression in NSCLC specimens increased relative to that in adjacent normal tissues and was further elevated in metastatic lymph nodes. The specimens acquired from 25 patients confirmed these findings. Additionally, circ_0109320 indicated a good score (AUC = 0.688, P = 0.013) on the ROC curves, which suggests its suitability as a promising biomarker for lung cancer. Meanwhile, circ_0109320 was noticeably upregulated in lung cancer (LC) cell lines compared to human bronchial epithelial cells. Next, we performed loss- and gain-of-function experiments to examine the role of circ_0109320 in the tumor phenotypes of the cell lines. We observed that depletion or overexpression of circ_0109320 did not alter cell viability. However, the ectopic removal of circ_0109320 repressed the migration and invasion of A549 and SK-MES-1 cells, whereas circ_0109320 overexpression promoted cell migration and invasion. Furthermore, the examination of epithelial-mesenchymal transition (EMT) markers indicated that circ_0109320 elevates cell EMT activity. In conclusion, circ_0109320 level was highly associated with increased tumor cell proliferation and metastasis. circ_0109320 could be a promising predictor of clinical outcomes and a reliable target to treat NSCLC by inhibiting metastasis.

Hsa_circ_0109320 通过促进转移成为非小细胞肺癌的新型环状 RNA 生物标记物
非小细胞肺癌(NSCLC)包括鳞状细胞癌和腺癌,是全球发病率和死亡率最高的十大癌症之一。NSCLC 是一种高度恶性肿瘤,具有远处侵袭和迁移的特点,预后不良。作为一种创新的环状 RNA,hsa _circ_0109320(circ_0109320)已被认为是一种很有前景的癌症调节剂。然而,我们对circ_0109320在NSCLC中的影响的了解仍然不足。我们的研究探讨了 circ_0109320 的临床意义及其对非小细胞肺癌(NSCLC)致癌表型的影响。微阵列分析和 qPCR 显示,与邻近正常组织相比,circ_0109320 在 NSCLC 标本中的表达增加,在转移淋巴结中的表达进一步升高。25 名患者的标本证实了这些发现。此外,circ_0109320 在 ROC 曲线上显示出良好的得分(AUC = 0.688,P = 0.013),这表明它适合作为肺癌的生物标记物。同时,与人类支气管上皮细胞相比,circ_0109320在肺癌细胞系中明显上调。接下来,我们进行了功能缺失和功能增益实验,研究 circ_0109320 在细胞系肿瘤表型中的作用。我们观察到,circ_0109320的缺失或过表达并不会改变细胞的活力。然而,异位删除 circ_0109320 会抑制 A549 和 SK-MES-1 细胞的迁移和侵袭,而过表达 circ_0109320 则会促进细胞的迁移和侵袭。此外,上皮-间质转化(EMT)标记物的检测表明,circ_0109320 能提高细胞的 EMT 活性。总之,circ_0109320水平与肿瘤细胞增殖和转移高度相关。circ_0109320可能是预测临床结果的一个有希望的指标,也是通过抑制转移治疗NSCLC的一个可靠靶点。
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来源期刊
Molecular Biotechnology
Molecular Biotechnology 医学-生化与分子生物学
CiteScore
4.10
自引率
3.80%
发文量
165
审稿时长
6 months
期刊介绍: Molecular Biotechnology publishes original research papers on the application of molecular biology to both basic and applied research in the field of biotechnology. Particular areas of interest include the following: stability and expression of cloned gene products, cell transformation, gene cloning systems and the production of recombinant proteins, protein purification and analysis, transgenic species, developmental biology, mutation analysis, the applications of DNA fingerprinting, RNA interference, and PCR technology, microarray technology, proteomics, mass spectrometry, bioinformatics, plant molecular biology, microbial genetics, gene probes and the diagnosis of disease, pharmaceutical and health care products, therapeutic agents, vaccines, gene targeting, gene therapy, stem cell technology and tissue engineering, antisense technology, protein engineering and enzyme technology, monoclonal antibodies, glycobiology and glycomics, and agricultural biotechnology.
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