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长链非编码RNA DGUOK-AS1通过调控miR-653-5p/SLC6A15轴促进肺鳞状细胞癌的细胞进展。

LncRNA DGUOK-AS1 Promotes Cell Progression in Lung Squamous Cell Carcinoma by Regulation of miR-653-5p/SLC6A15 Axis.

作者信息

Teng Yan, Li Shixia, Wei Lijuan, Zhang Chi, Li Lijuan, Wang Shuang, Zhang Jing, Huang Jinchao, Zhang Huan, Wu Nan, Liu Juntian

机构信息

Key Laboratory of Cancer Prevention and Therapy, Tianjin, Tianjin's Clinical Research Center for Cancer, Tianjin Medical University Cancer Institute & Hospital, National Clinical Research Center for Cancer, Tianjin, 300060, China.

出版信息

Mol Biotechnol. 2025 Feb;67(2):734-745. doi: 10.1007/s12033-024-01088-8. Epub 2024 Feb 26.

Abstract

Long noncoding RNA (lncRNA) plays a key role in regulating cancer development. LncRNA deoxyguanosine kinase antisense RNA 1 (DGUOK-AS1) has been reported as a promoter in tumor. The work was designed to further investigate the mechanism of action of DGUOK-AS1 in lung squamous cell carcinoma (LUSC). DGUOK-AS1 level in LUSC cells was measured using RT-qPCR. Counting Kit-8 assays and colony forming assays were performed to evaluate LUSC cell viability and proliferation. Transwell assays were performed to detect cell migration and invasion. Luciferase reporter and RNA pulldown assays were used to verify the binding capacity of DGUOK-AS1 and miR-653-5p. RNA immunoprecipitation assays were performed to verify the relationship of DGUOK-AS1, miR-653-5p, and SLC6A15. DGUOK-AS1 was highly expressed in LUSC cells. DGUOK-AS1 knockdown suppressed LUSC cell proliferation, migration, and invasion. SLC6A15 was demonstrated to be targeted by miR-653-5p, and DGUOK-AS1 interacted with miR-653-5p to modulate SLC6A15 level in LUSC cells. Overexpression of SLC6A15 reversed the suppressive effects of DGUOK-AS1 knockdown on LUSC cell processes. In conclusion, DGUOK-AS1 promotes malignant behaviors of LUSC cells by upregulating SLC6A15 level through interaction with miR-653-5p.

摘要

长链非编码RNA(lncRNA)在调节癌症发展中起关键作用。据报道,lncRNA脱氧鸟苷激酶反义RNA 1(DGUOK-AS1)是一种肿瘤启动子。本研究旨在进一步探究DGUOK-AS1在肺鳞状细胞癌(LUSC)中的作用机制。采用RT-qPCR检测LUSC细胞中DGUOK-AS1的水平。进行细胞计数试剂盒-8检测和集落形成检测以评估LUSC细胞的活力和增殖。进行Transwell检测以检测细胞迁移和侵袭。使用荧光素酶报告基因检测和RNA下拉检测来验证DGUOK-AS1与miR-653-5p的结合能力。进行RNA免疫沉淀检测以验证DGUOK-AS1、miR-653-5p和SLC6A15之间的关系。DGUOK-AS1在LUSC细胞中高表达。敲低DGUOK-AS1可抑制LUSC细胞的增殖、迁移和侵袭。结果表明SLC6A15是miR-653-5p的靶标,并且DGUOK-AS1与miR-653-5p相互作用以调节LUSC细胞中SLC6A15的水平。过表达SLC6A15可逆转敲低DGUOK-AS1对LUSC细胞进程的抑制作用。总之,DGUOK-AS1通过与miR-653-5p相互作用上调SLC6A15水平,从而促进LUSC细胞的恶性行为。

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