Hsa_circ_0001640通过靶向MiR-942-5p/PTEN轴使PI3K/AKT信号通路失活,抑制非小细胞肺癌的进展

IF 3.5 3区 生物学 Q3 CELL BIOLOGY
Yanting Wang , Xinlin Wang , Tao Zhang , Xin He
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引用次数: 0

摘要

非小细胞肺癌(Non-small cell lung cancer, NSCLC)是肺癌的主要病理类型,发病率和死亡率都很高。为了鉴定特异性生物标志物,我们对非小细胞肺癌中异常表达的环状rna (circRNAs)进行了表征。我们发现hsa_circ_0001640在NSCLC组织和细胞系中表达下调。过表达hsa_circ_0001640抑制NSCLC细胞的增殖、侵袭和迁移,促进细胞凋亡。双荧光素酶测定证实了hsa_circ_0001640和miR-942-5p之间的相互作用。miR-942-5p与hsa_circ_0001640共转染部分逆转了hsa_circ_0001640过表达对肿瘤细胞生物学行为的影响。机制上,hsa_circ_0001640通过靶向miR-942-5p/PTEN轴使PI3K/AKT信号通路失活,从而抑制NSCLC的进展。此外,体内实验表明,过表达hsa_circ_0001640可抑制小鼠异种移植瘤的生长。我们的发现将为非小细胞肺癌的诊断和治疗提供新的标志物和可能的靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hsa_circ_0001640 inactivation of the PI3K/AKT signaling pathway by targeting the MiR-942-5p/PTEN axis to inhibit the progression of non-small cell lung cancer
Non-small cell lung cancer (NSCLC) is the main pathological type of lung cancer with high morbidity and mortality. To identify specific biomarkers, we characterized aberrantly expressed circular RNAs (circRNAs) in NSCLC. We found that hsa_circ_0001640 expression was downregulated in NSCLC tissues and cell lines. Overexpression of hsa_circ_0001640 inhibited proliferation, invasion and migration, and promoted apoptosis in NSCLC cells.Dual-luciferase assays confirmed the interaction between hsa_circ_0001640 and miR-942-5p. Co-transfection of miR-942-5p with hsa_circ_0001640 partially reversed the effects of hsa_circ_0001640 overexpression on tumor cell biological behaviors. Mechanistically, hsa_circ_0001640 inactivated the PI3K/AKT signaling pathway by targeting the miR-942-5p/PTEN axis, thereby suppressing NSCLC progression. Furthermore, in vivo experiments demonstrated that overexpression of hsa_circ_0001640 suppressed the growth of xenograft tumors in mice.Our findings will provide a new marker and possible target for the diagnosis and treatment of NSCLC.
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来源期刊
Experimental cell research
Experimental cell research 医学-细胞生物学
CiteScore
7.20
自引率
0.00%
发文量
295
审稿时长
30 days
期刊介绍: Our scope includes but is not limited to areas such as: Chromosome biology; Chromatin and epigenetics; DNA repair; Gene regulation; Nuclear import-export; RNA processing; Non-coding RNAs; Organelle biology; The cytoskeleton; Intracellular trafficking; Cell-cell and cell-matrix interactions; Cell motility and migration; Cell proliferation; Cellular differentiation; Signal transduction; Programmed cell death.
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