Circular RNA sirtuin-1 restrains the malignant phenotype of non-small cell lung cancer cells via the microRNA-510-5p/SMAD family member 7 axis.

IF 1.4 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
ZiRan Zhao, HongYan Zhang, Fan Zhang, Ying Ji, Yue Peng, Fei Wang, Liang Zhao
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引用次数: 0

Abstract

Circular RNA (circRNA) sirtuin-1 (SIRT1) is differentially expressed in non-small cell lung cancer (NSCLC), but its specific mechanism is still uncertain. The study was to figure out the latent molecular mechanism of circSIRT1 in NSCLC. The results clarified that circSIRT1 and SMAD family member 7 (SMAD7) were downregulated, but microRNA (miR)-510-5p was upregulated in NSCLC. CircSIRT1 expression was linked with tumor-node-metastasis staging and tumor size in NSCLC patients. Elevating circSIRT1 or suppressing miR-510-5p refrained NSCLC cell activities and glycolysis and inactivated the wnt/β-catenin pathway, while knockdown of circSIRT1 promoted the malignant behavior of NSCLC cells. Besides, inhibition of malignant behavior in NSCLC cells by elevating circSIRT1 was reversed by knockdown of SMDA7. circSIRT1 bound to miR-510-5p to target SMAD7. In short, circSIRT1 represses NSCLC cell malignant development via miR-510-5p to target SMAD7, making it a latent target for NSCLC treatment.

环状RNA sirtuin-1通过微小RNA-510-5p/SMAD家族成员7轴抑制非小细胞肺癌癌症细胞的恶性表型。
环状RNA(circRNA)sirtuin-1(SIRT1)在癌症(NSCLC)中差异表达,但其具体机制尚不确定。本研究旨在探讨circSIRT1在NSCLC中的潜在分子机制。结果表明,在NSCLC中,circSIRT1和SMAD家族成员7(SMAD7)下调,但微小RNA(miR)-510-5p上调。CircSIRT1的表达与NSCLC患者的肿瘤淋巴结转移分期和肿瘤大小有关。升高circSIRT1或抑制miR-510-5p抑制了NSCLC细胞的活性和糖酵解,并使wnt/β-catenin通路失活,而敲低circSIRT1则促进了NSCLC的恶性行为。此外,通过升高circSIRT1对NSCLC细胞恶性行为的抑制作用被SMDA7的敲除所逆转。circSIRT1与miR-510-5p结合以靶向SMAD7。简而言之,circSIRT1通过miR-510-5p靶向SMAD7来抑制NSCLC细胞的恶性发展,使其成为NSCLC治疗的潜在靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Acta biochimica Polonica
Acta biochimica Polonica 生物-生化与分子生物学
CiteScore
2.40
自引率
0.00%
发文量
99
审稿时长
4-8 weeks
期刊介绍: Acta Biochimica Polonica is a journal covering enzymology and metabolism, membranes and bioenergetics, gene structure and expression, protein, nucleic acid and carbohydrate structure and metabolism.
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