Circ_0000735通过调节miR-635/FAM83F轴促进非小细胞肺癌的增殖、转移和糖酵解。

IF 1.5 4区 医学 Q3 RESPIRATORY SYSTEM Experimental Lung Research Pub Date : 2021-04-01 Epub Date: 2021-02-09 DOI:10.1080/01902148.2021.1881188
Guigang Tai, Miao Zhang, Fang Liu
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引用次数: 11

摘要

背景:环状RNA (circRNA)被认为是包括非小细胞肺癌(NSCLC)在内的癌症恶性进展的重要调节因子。Circ_0000735已被发现与NSCLC进展相关。因此,其在NSCLC中的作用和分子机制值得进一步探讨。方法:采用实时荧光定量PCR (qRT-PCR)检测circ_0000735、microRNA (miR)-635及序列相似家族83成员F (FAM83F)的表达情况。采用细胞计数试剂盒8法、集落形成法、transwell法和流式细胞术检测细胞增殖、迁移、侵袭和凋亡。通过检测细胞的葡萄糖消耗和乳酸生成来测量细胞糖酵解。Western blot检测糖酵解标志物和FAM83F蛋白水平。circ_0000735与miR-635或miR-635与FAM83F之间的关系通过双荧光素酶报告基因实验验证。通过构建异种移植模型评估circ_0000735对NSCLC肿瘤生长的影响。结果:Circ_0000735在NSCLC中是一个高表达的circRNA。沉默circ_0000735可抑制NSCLC细胞的增殖、迁移、侵袭、糖酵解,并增加细胞凋亡。MiR-635可以被circ_0000735擦拭,其抑制剂可以逆转circ_0000735沉默对NSCLC进展的调节。此外,FAM83F是miR-635的靶标,circ_0000735通过海绵化miR-635正向调节FAM83F。miR-635对NSCLC进展的抑制作用也可以被FAM83F过表达逆转。此外,circ_0000735敲低通过调节miR-635/FAM83F轴降低NSCLC肿瘤生长。结论:Circ_0000735通过miR-635/FAM83F轴促进NSCLC进展,表明Circ_0000735可能是一种有前景的NSCLC生物标志物。重点:Circ_0000735敲低抑制NSCLC细胞进展和肿瘤生长。Circ_0000735作为miR-635海绵。FAM83F是miR-635的靶点。
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Circ_0000735 enhances the proliferation, metastasis and glycolysis of non-small cell lung cancer by regulating the miR-635/FAM83F axis.

Background: Circular RNA (circRNA) is considered to be an important regulator of cancer malignant progression, including non-small cell lung cancer (NSCLC). Circ_0000735 has been found to be associated with NSCLC progression. Therefore, its role and molecular mechanism in NSCLC deserve further exploration.

Methods: Quantitative real-time PCR (qRT-PCR) was used to measure the expression of circ_0000735, microRNA (miR)-635 and family with sequence similarity 83 member F (FAM83F). Cell proliferation, migration, invasion and apoptosis were determined using cell counting kit 8 assay, colony formation assay, transwell assay and flow cytometry. Cell glycolysis were measured by detecting the glucose consumption and lactate production of cells. Western blot analysis was utilized to test the protein levels of glycolysis markers and FAM83F. The relationship between circ_0000735 and miR-635 or miR-635 and FAM83F was verified by dual-luciferase reporter assay. The effect of circ_0000735 on NSCLC tumor growth was evaluated by constructing xenograft models.

Results: Circ_0000735 was a highly expressed circRNA in NSCLC. Silenced circ_0000735 could inhibit NSCLC cell proliferation, migration, invasion, glycolysis, and increase apoptosis. MiR-635 could be sponged by circ_0000735, and its inhibitor could reverse the regulation of circ_0000735 silencing on NSCLC progression. Moreover, FAM83F was a target of miR-635, and circ_0000735 positively regulated FAM83F by sponging miR-635. The inhibitory effect of miR-635 on NSCLC progression could also be reversed by FAM83F overexpression. Additionally, circ_0000735 knockdown reduced NSCLC tumor growth through regulating miR-635/FAM83F axis.

Conclusion: Circ_0000735 promoted NSCLC progression by the miR-635/FAM83F axis, showing that circ_0000735 might be a promising biomarker for NSCLC. Highlights: Circ_0000735 knockdown represses NSCLC cell progression and tumor growth. Circ_0000735 functions as a miR-635 sponge. FAM83F is targeted by miR-635.

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来源期刊
Experimental Lung Research
Experimental Lung Research 医学-呼吸系统
CiteScore
3.80
自引率
0.00%
发文量
23
审稿时长
2 months
期刊介绍: Experimental Lung Research publishes original articles in all fields of respiratory tract anatomy, biology, developmental biology, toxicology, and pathology. Emphasis is placed on investigations concerned with molecular, biochemical, and cellular mechanisms of normal function, pathogenesis, and responses to injury. The journal publishes reports on important methodological advances on new experimental modes. Also published are invited reviews on important and timely research advances, as well as proceedings of specialized symposia. Authors can choose to publish gold open access in this journal.
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