Ou Deming, Wu Ying, Liu Jun, Lao Xiaomei, Zhang Sien, Liao Guiqing
Department of Oral and Maxillofacial Surgery, Guanghua School of Stomatology, Guangdong Provincial Key Laboratory of Stomatology, Sun Yat-Sen University, Guangzhou, Guangdong 510055, P.R. China; Department of Stomatology, Central Hospital of Panyu, Guangzhou, Guangdong 511400, P.R. China.
Department of Stomatology, Foshan Hospital of Chinese Traditional Medicine, Foshan, Guangdong 528000 P.R. China.
Oncol Lett. 2016 Oct;12(4):2531-2537. doi: 10.3892/ol.2016.4938. Epub 2016 Aug 3.
The aim of the present study was to characterize the roles of two microRNAs (miRs) that have been reported to be differentially expressed in tongue squamous cell carcinoma (TSCC), miR-335 and miR-182. In total, 20 tumor tissue samples and 20 corresponding adjacent non-cancerous samples were collected from patients with TSCC to measure the expression of miR-335 and miR-182 and the potential shared target of these miRs, survivin, using reverse transcription-quantitative polymerase chain reaction and western blotting. In the TSCC tissue samples, significantly decreased expression of the two miRs and increased expression of survivin were detected compared with adjacent non-cancerous controls. Subsequently, it was confirmed that survivin was the target gene of miR-335 and miR-182 using a luciferase assay in TSCC cells. In order to examine the function of miR-335 and miR-182 in the development of TSCC, TSCC cells were transiently transfected with the mimics of the two miRs, and it was confirmed that the introduction of miR-335 and miR-182 to cells suppressed the expression of survivin and markedly inhibited the proliferation of the TSCC cells. Furthermore, miR-335 and miR-182 were found to induce cell cycle arrest by suppressing the expression of survivin. The present study revealed a negative regulatory role of miR-335 and miR-182 in the proliferation of TSCC cells by targeting survivin, and miR-335 and miR-182 may be novel therapeutic targets for the treatment of TSCC.
本研究的目的是明确两种据报道在舌鳞状细胞癌(TSCC)中差异表达的微小RNA(miR),即miR-335和miR-182的作用。总共从TSCC患者中收集了20个肿瘤组织样本和20个相应的相邻非癌样本,采用逆转录定量聚合酶链反应和蛋白质印迹法检测miR-335和miR-182的表达以及这些miR潜在的共同靶标生存素。与相邻非癌对照相比,在TSCC组织样本中检测到这两种miR的表达显著降低,而生存素的表达增加。随后,在TSCC细胞中使用荧光素酶测定法证实生存素是miR-335和miR-182的靶基因。为了研究miR-335和miR-182在TSCC发生发展中的作用,用这两种miR的模拟物瞬时转染TSCC细胞,证实将miR-335和miR-182导入细胞可抑制生存素的表达并显著抑制TSCC细胞的增殖。此外,发现miR-335和miR-182通过抑制生存素的表达诱导细胞周期停滞。本研究揭示了miR-335和miR-182通过靶向生存素对TSCC细胞增殖具有负调控作用,并且miR-335和miR-182可能是治疗TSCC的新的治疗靶点。