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基于 microRNA 表达谱鉴定下咽鳞癌中的肿瘤抑制 microRNA-451a。

Identification of tumour suppressive microRNA-451a in hypopharyngeal squamous cell carcinoma based on microRNA expression signature.

机构信息

1] Department of Functional Genomics, Chiba University Graduate School of Medicine, Chiba, Japan [2] Department of Otorhinolaryngology/Head and Neck Surgery, Chiba University Graduate School of Medicine, Chiba, Japan.

Department of Otorhinolaryngology/Head and Neck Surgery, Chiba University Graduate School of Medicine, Chiba, Japan.

出版信息

Br J Cancer. 2014 Jul 15;111(2):386-94. doi: 10.1038/bjc.2014.293. Epub 2014 Jun 10.

Abstract

BACKGROUND

Hypopharyngeal squamous cell carcinoma (HSCC) has a very poor prognosis because of its high rates of regional and distant metastasis. Identification of differentially expressed miRNAs and their regulated molecular targets in tumour cells might enhance our understanding of the molecular mechanisms of metastasis in human cancers.

METHODS

A HSCC miRNA signature was constructed by array-based methods. Functional studies of microRNA-451a (miR-451a) and target genes were performed to investigate cell proliferation, migration and invasion by cancer cell lines. To identify miR-451a-regulated molecular targets, we adopted gene expression analysis and in silico database analysis.

RESULTS

Our miRNA signature revealed that miR-451a was significantly downregulated in HSCC. Restoration of miR-451a in cancer cell lines revealed that this miRNA significantly inhibited cancer cell migration and invasion. Our data demonstrated that the gene coding for endothelial and smooth muscle cell-derived neuropilin-like molecule (ESDN/DCBLD2) was a direct target of miR-451a regulation. Silencing of ESDN inhibited cell migration and invasion by cancer cells.

CONCLUSIONS

Loss of tumour suppressive miR-451a enhanced cancer cell migration and invasion in HSCC through direct regulation of ESDN. Our miRNA signature and functional analysis of targets regulated by tumour suppressive miR-451a provide new insights into the potential mechanisms of HSCC oncogenesis and metastasis.

摘要

背景

下咽鳞状细胞癌(HSCC)由于其较高的区域和远处转移率,预后非常差。鉴定肿瘤细胞中差异表达的 miRNA 及其调控的分子靶标可能会增强我们对人类癌症转移分子机制的理解。

方法

通过基于阵列的方法构建 HSCC miRNA 特征。通过癌细胞系进行 microRNA-451a(miR-451a)和靶基因的功能研究,以研究细胞增殖、迁移和侵袭。为了鉴定 miR-451a 调控的分子靶标,我们采用了基因表达分析和计算机数据库分析。

结果

我们的 miRNA 特征表明 miR-451a 在 HSCC 中显著下调。在癌细胞系中恢复 miR-451a 后,发现该 miRNA 显著抑制了癌细胞的迁移和侵袭。我们的数据表明,内皮细胞和平滑肌细胞衍生的神经纤毛蛋白样分子(ESDN/DCBLD2)的编码基因是 miR-451a 调节的直接靶标。ESDN 的沉默抑制了癌细胞的迁移和侵袭。

结论

肿瘤抑制性 miR-451a 的丢失通过直接调节 ESDN 增强了 HSCC 中癌细胞的迁移和侵袭。我们的 miRNA 特征和受肿瘤抑制性 miR-451a 调控的靶基因的功能分析为 HSCC 发生和转移的潜在机制提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35c9/4102946/961749f30b57/bjc2014293f1.jpg

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