Department of Functional Genomics, Chiba University Graduate School of Medicine, 1-8-1 Inohana Chuo-ku, Chiba 260-8670, Japan.
Br J Cancer. 2011 Sep 6;105(6):833-41. doi: 10.1038/bjc.2011.311. Epub 2011 Aug 16.
On the basis of the microRNA (miRNA) expression signature of maxillary sinus squamous cell carcinoma (MSSCC), we found that miR-874 was significantly reduced in cancer cells. We focused on the functional significance of miR-874 in cancer cells and identification of miR-874-regulated novel cancer networks in MSSCC.
We used PCR-based methods to investigate the downregulated miRNAs in clinical specimens of MSSCC. Our signature analyses identified 23 miRNAs that were significantly reduced in cancer cells, such as miR-874, miR-133a, miR-375, miR-204, and miR-1. We focused on miR-874 as the most downregulated novel miRNA in our analysis.
We found potential tumour suppressive functions such as inhibition of cancer cell proliferation and invasion. A molecular target search of miR-874 revealed that PPP1CA was directly regulated by miR-874. Overexpression of PPP1CA was observed in MSSCC clinical specimens. Silencing of the PPP1CA gene significantly inhibited cancer cell proliferation and invasion.
The downregulation of miR-874 was a frequent event in MSSCC, which suggests that miR-874 functions as a tumour suppressive miRNA, directly regulating PPP1CA that has a potential role of an oncogene. The identification of novel miR-874-regulated cancer pathways could provide new insights into potential molecular mechanisms of MSSCC oncogenesis.
基于上颌窦鳞状细胞癌(MSSCC)的 miRNA(miRNA)表达特征,我们发现癌细胞中 miR-874 显著降低。我们专注于 miR-874 在癌细胞中的功能意义,并鉴定 MSSCC 中 miR-874 调节的新型癌症网络。
我们使用基于 PCR 的方法来研究 MSSCC 临床标本中下调的 miRNA。我们的特征分析确定了 23 种 miRNA 在癌细胞中显著降低,如 miR-874、miR-133a、miR-375、miR-204 和 miR-1。我们专注于 miR-874,因为它是我们分析中下调最明显的新型 miRNA。
我们发现了潜在的肿瘤抑制功能,如抑制癌细胞增殖和侵袭。miR-874 的分子靶标搜索显示 PPP1CA 被 miR-874 直接调控。PPP1CA 在 MSSCC 临床标本中过表达。沉默 PPP1CA 基因显著抑制了癌细胞的增殖和侵袭。
miR-874 的下调是 MSSCC 中的一个常见事件,这表明 miR-874 作为肿瘤抑制 miRNA 发挥作用,直接调控 PPP1CA,后者可能具有癌基因的作用。鉴定新型 miR-874 调节的癌症途径可以为 MSSCC 致癌的潜在分子机制提供新的见解。