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首页> 外文期刊>OncoTargets and therapy >lncRNA NEAT1 Facilitates Cell Proliferation, Invasion and Migration by Regulating CBX7 and RTCB in Breast Cancer
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lncRNA NEAT1 Facilitates Cell Proliferation, Invasion and Migration by Regulating CBX7 and RTCB in Breast Cancer

机译:LNCRNA Neat1通过调节乳腺癌中的CBX7和RTCB来促进细胞增殖,侵袭和迁移

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Purpose: To investigate the association between the lncRNA NEAT1 and breast cancer, and to determine the influence of NEAT1 on regulation of other signaling molecules in breast cancer. Methods: In the present study, we measured levels of the lncRNA NEAT1 in 106 breast cancer patients and in a human breast cancer cell line by qRT-PCR. The correlation between NEAT1 expression and patients’ clinical characteristics was analyzed with in-house and TCGA data. We used cellular functioning assays and cell immunofluorescence assay to evaluate the role of NEAT1 and its target molecules in proliferation, invasion and migration in breast cancer. We used Western blotting to explore possible targets of NEAT1 and a subcellular fractionation assay to locate NEAT1 expression. Results: NEAT1 was overexpressed in breast cancer tissue and also closely related to advanced clinical stages and positive lymph node metastases. NEAT1 levels were also tightly correlated to prognosis for breast cancer patients in survival analyses. Cellular function assays revealed that downregulation of NEAT1 could inhibit breast cancer cell viability, invasion and migration. Western blotting revealed down-regulation of CBX7 and up-regulation of RTCB following NEAT1 inhibition. Based on the cytoplasmic and nuclear expression of NEAT1, we investigated the possible regulation of CBX7 and RTCB by NEAT1. Results showed that NEAT1 regulated the expression of CBX7 and RTCB, possibly by binding of NEAT1 to DNA in the nucleus, which facilitates cell proliferation, invasion and migration. Conclusion: The current results suggest that the lncRNA NEAT1 is upregulated in breast cancer and facilitates tumor cell viability, invasion and migration via CBX7 and RTCB.
机译:目的:探讨LNCRNA Neat1和乳腺癌之间的关联,并确定Neat1对乳腺癌其他信号分子调节的影响。方法:在本研究中,通过QRT-PCR测量106例乳腺癌患者和人乳腺癌细胞系中LNCRNA Neat1的水平。内部和TCGA数据分析了Neat1表达与患者的临床特征之间的相关性。我们使用细胞功能测定和细胞免疫荧光测定来评估Neat1及其靶分子在乳腺癌中的增殖,侵袭和迁移中的作用。我们使用Western Blotting来探讨Neat1和亚细胞分馏测定的可能靶标以定位Neat1表达。结果:Neat1在乳腺癌组织中过表达,也与晚期临床阶段和阳性淋巴结转移相关。 Neat1水平与存活分析中的乳腺癌患者的预后也紧密相关。细胞功能测定显示,Neat1的下调可以抑制乳腺癌细胞活力,入侵和迁移。蛋白质印迹显示CBX7的下调和Neat1抑制后RTCB的上调。基于Neat1的细胞质和核表达,我们通过Neat1调查了CBX7和RTCB的可能调节。结果表明,Neat1调节CBX7和RTCB的表达,可能是通过Neat1与细胞核中的DNA结合,这有助于细胞增殖,侵袭和迁移。结论:目前的结果表明,LNCRNA Neat1在乳腺癌中上调,促进肿瘤细胞活力,侵袭和迁移通过CBX7和RTCB。

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