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首页> 外文期刊>OncoTargets and therapy >LncRNA LINC00665 Promotes Prostate Cancer Progression via miR-1224-5p/SND1 Axis
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LncRNA LINC00665 Promotes Prostate Cancer Progression via miR-1224-5p/SND1 Axis

机译:LNCRNA LINC00665通过MIR-1224-5P / SND1轴促进前列腺癌进展

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Background: Increasing researches have revealed a critical role of long noncoding RNAs (lncRNAs) in tumor progression. LINC00665 is a poorly investigated lncRNA. In this research, we sought to determine the potential role of LINC00665 in prostate cancer (PC) progression. Methods: LINC00665 expression was analyzed by bioinformatics method and qRT-PCR. Proliferation was determined via CCK8 and colony formation assays. Transwell assay was conducted to analyze migration and invasion. Xenograft assay was used to test the roles of LINC00665 in vivo. Luciferase reporter assay, pulldown assay and RIP assay were utilized to confirm the interaction between LINC00665 and miR-1224-5p. Results: LINC00665 expression was increased in PC samples in contrast to control tissues, according to bioinformatics analysis and qRT-PCR validation. LINC00665 high expression was related to a poor prognosis. LINC00665 knockdown markedly attenuated growth and metastasis of PC cells and impaired tumor propagation in vivo. Mechanistic investigation revealed that?LINC00665 was the sponge for miR-1224-5p. By inhibiting miR-1224-5p level, LINC00665 dramatically promoted the expression of SND1 in PC cells. Ectopic expression of SND1 significantly rescued the effects of LINC00665 silencing. Conclusion: LINC00665 is a novel oncogenic gene in PC by targeting miR-1224-5p/SND1 pathway and may be a therapeutic target.
机译:背景:越来越多的研究揭示了长期非编码RNA(LNCRNA)在肿瘤进展中的关键作用。 LINC00665是一个较差的LNCRNA。在这项研究中,我们试图确定LINC00665在前列腺癌(PC)进展中的潜在作用。方法:通过生物信息学方法和QRT-PCR分析LINC00665表达。通过CCK8和菌落形成测定测定增殖。进行Transwell测定以分析迁移和侵袭。异种移植测定用于测试LINC00665在体内的作用。荧光素酶报告器测定,下拉测定和RIP测定用于证实LINC00665和MIR-1224-5P之间的相互作用。结果:根据生物信息学分析和QRT-PCR验证,PC样品中的PC样品中LINC00665表达升高。 LINC00665高表达与预后差有关。 LINC00665敲低明显减弱PC细胞的生长和转移,体内肿瘤繁殖受损。机械调查显示:LINC00665是MIR-1224-5P的海绵。通过抑制miR-1224-5P水平,LINC00665显着促进了PC细胞中SND1的表达。 SND1的异位表达显着拯救了LINC00665沉默的影响。结论:LINC00665是通过靶向MIR-1224-5P / SND1途径PC中的新型致癌基因,并且可以是治疗靶标。

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