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首页> 外文期刊>Cancer Medicine >Interference of the long noncoding RNA CDKN2B‐AS1 upregulates miR‐181a‐5p/TGFβI axis to restrain the metastasis and promote apoptosis and senescence of cervical cancer cells
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Interference of the long noncoding RNA CDKN2B‐AS1 upregulates miR‐181a‐5p/TGFβI axis to restrain the metastasis and promote apoptosis and senescence of cervical cancer cells

机译:长非编码RNA CDKN2B‐AS1的干扰会上调miR‐181a‐5p /TGFβI轴以抑制转移并促进子宫颈癌细胞的凋亡和衰老

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Long noncoding RNA (lncRNA) CDKN2B‐AS1 has been shown to play a crucial role in the development as well as in the prognosis of various human cancers, including cervical cancer. However, the underlying mechanisms need to be further explored between CDKN2B‐AS1 and cervical cancer. In the present study, RT‐PCR showed that the mRNA level of CDKN2B‐AS1 was significantly upregulated while the miR‐181a‐5p was downregulated in cervical cancer cell lines. In addition, the interference of CDKN2B‐AS1 by shRNA resulted in the suppression of cell proliferation, invasion, migration and promotion of apoptosis and senescence, and either CDKN2B‐AS1 overexpression or miR‐181a‐5p showed reversed results. Further studies demonstrated that CDKN2B‐AS1 could directly interact with miR‐181a‐5p, and that there was an inverse correlation between miR‐181a‐5p and CDKN2B‐AS1. In addition, we found that TGFβI was a target of miR‐181a‐5p and could be downregulated by CDKN2B‐AS1 knockdown. Moreover, the in vivo experiments further demonstrated the contribution of CDKN2B‐AS1 in cervical cancer including tumor growth, apoptosis inhibition and senescence inhibition, and CDKN2B‐AS1 knockdown could inhibit the aforementioned activities. In summary, our study demonstrated that the CDKN2B‐AS1/miR‐181a‐5p/TGFβI axis might play a vital role in cervical cancer development.
机译:长非编码RNA(lncRNA)CDKN2B‐AS1已被证明在包括宫颈癌在内的各种人类癌症的发生以及预后中起着至关重要的作用。但是,在CDKN2B‐AS1与宫颈癌之间需要进一步探索其潜在机制。在本研究中,RT-PCR显示在宫颈癌细胞系中CDKN2B-AS1的mRNA水平显着上调,而miR-181a-5p则下调。此外,shRNA干扰CDKN2B‐AS1会抑制细胞增殖,侵袭,迁移并促进凋亡和衰老,而CDKN2B‐AS1的过表达或miR‐181a‐5p的结果相反。进一步的研究表明CDKN2B‐AS1可以直接与miR‐181a‐5p相互作用,并且miR‐181a‐5p与CDKN2B‐AS1之间存在反相关关系。此外,我们发现TGFβI是miR‐181a‐5p的靶标,并可能通过CDKN2B‐AS1敲低而下调。此外,体内实验进一步证明了CDKN2B‐AS1在子宫颈癌中的作用,包括肿瘤生长,凋亡抑制和衰老抑制作用,而CDKN2B‐AS1的敲除可以抑制上述活性。总而言之,我们的研究表明CDKN2B‐AS1 / miR‐181a‐5p /TGFβI轴可能在宫颈癌的发展中起着至关重要的作用。

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