Stomatological Hospital of Guangdong Province Affiliated to Southern Medical University, Guangzhou, Guangdong 510280, P.R. China.
Department of Molecular Biology, Guangzhou Medical College, Guangzhou, Guangdong 510120, P.R. China.
Oncol Rep. 2014 Feb;31(2):867-73. doi: 10.3892/or.2013.2903. Epub 2013 Dec 6.
microRNAs (miRNAs) are aberrantly expressed in cancer. An enzyme essential for miRNA processing is Dicer, whose expression is deregulated in diverse types of cancer and correlates with tumor progression. However, whether the regulation of Dicer expression affects tongue squamous cell carcinoma is unknown. In the present study, we investigated how silencing the expression of Dicer alters cell proliferation, cell cycle patterns, and cell migration and invasion in the Tca-8113 tongue squamous cell carcinoma cell line. Dicer expression levels were determined using quantitative PCR and western blot analysis in normal oral gingival epithelial cells and in two tongue squamous cell carcinoma lines, Tca-8113 and UM-1. Tca-8113 cells were transfected with Dicer siRNA or a negative control siRNA. Cell proliferation was determined using the MTT assay and the cell cycle was examined using flow cytometry. Cell migration and invasion changes were evaluated using wound-healing, adherence and Transwell assays. Dicer was expressed at lower levels in the tongue squamous cell carcinoma cell lines Tca-8113 and UM-1 compared to normal gingival epithelial cells, and less Dicer was expressed in UM-1 cells compared to Tca-8113 cells. Notably, Tca-8113 cells transfected with Dicer siRNA had significantly higher proliferative and invasive abilities than cells transfected with the negative control siRNA or non-transfected cells. Silencing Dicer may promote the progression of tongue squamous cell carcinoma. Dicer could serve a promising biomarker and a potential therapeutic target for tongue squamous cell carcinoma.
微小 RNA(miRNAs)在癌症中表达异常。一种对 miRNA 加工至关重要的酶是 Dicer,其在多种类型的癌症中表达失调,与肿瘤进展相关。然而,Dicer 表达的调节是否会影响舌鳞状细胞癌尚不清楚。在本研究中,我们研究了沉默 Dicer 的表达如何改变 Tca-8113 舌鳞状细胞癌细胞系中的细胞增殖、细胞周期模式以及细胞迁移和侵袭。使用定量 PCR 和 Western blot 分析在正常口腔牙龈上皮细胞和两种舌鳞状细胞癌细胞系 Tca-8113 和 UM-1 中确定 Dicer 表达水平。Tca-8113 细胞用 Dicer siRNA 或阴性对照 siRNA 转染。使用 MTT 测定法测定细胞增殖,并用流式细胞术检查细胞周期。通过划痕愈合、粘附和 Transwell 测定评估细胞迁移和侵袭变化。与正常牙龈上皮细胞相比,舌鳞状细胞癌细胞系 Tca-8113 和 UM-1 中 Dicer 的表达水平较低,而与 Tca-8113 细胞相比,UM-1 细胞中 Dicer 的表达水平较低。值得注意的是,转染 Dicer siRNA 的 Tca-8113 细胞比转染阴性对照 siRNA 的细胞或未转染的细胞具有更高的增殖和侵袭能力。沉默 Dicer 可能促进舌鳞状细胞癌的进展。Dicer 可作为舌鳞状细胞癌有前途的生物标志物和潜在的治疗靶点。