Expressions of miR-590 in Oral Lichen Planus and Oral Squamous Cell Carcinoma Tissues and Clinical Values

IF 0.3 4区 医学 Q4 ENGINEERING, BIOMEDICAL Journal of Hard Tissue Biology Pub Date : 2021-01-01 DOI:10.2485/jhtb.30.363
Wanlu Chen, Yong Zhou, Zhongxiong Ma, Yunde Xie
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Abstract

: To detect the expression of miR-590 in oral lichen planus (OLP) tissues and oral squamous cell carcinoma (OSCC) tissues, and to analyze the correlations with clinicopathological characteristics and prognosis of OSCC patients. The oral mucosa tissues were selected from 180 patients with OLP or OSCC. They were divided into OLP group (n=92) and OSCC group (n=88), and 40 healthy volunteers with normal oral mucosa tissues were set as control group. Human tongue squamous cell carcinoma cell line SCC9 and human oral keratinocyte HOK were used. The expressions of miR-590 in tissues and cells were detected using qPCR. SCC9 cells were transfected with small interfering (si)-miR-590 and si-NC plasmids. MTT assay, flow cytometry and Transwell assay were used to detect cell proliferation, apoptosis, migration and invasion abilities, respectively. The expression levels of apoptosis-, migration- and invasion-related proteins were examined using Western blotting. Control, OLP and OSCC groups displayed successively increased expression of miR-590, suggesting that the expression was related to the TNM stage and lymph node metastasis of OSCC patients (P<0.05). Following transfection with si-miR-590, the proliferation, migration and invasion abilities of SCC9 cells were weakened significantly, while the apoptosis rate rose (P<0.05). The expression levels of Bcl-2, N-cadherin and vimentin dropped significantly, whereas those of Bax and E-cadherin increased (P<0.05). MiR-590 is highly expressed in OSCC and SCC9 cells. Silencing miR-590 can suppress the proliferation, migration and invasion and promote the apoptosis of SCC9 cells.
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miR-590在口腔扁平苔藓和口腔鳞状细胞癌组织中的表达及临床意义
目的:检测miR-590在口腔扁平苔藓(OLP)组织和口腔鳞状细胞癌(OSCC)组织中的表达,分析其与OSCC患者临床病理特征及预后的相关性。选择180例OLP或OSCC患者的口腔黏膜组织。分为OLP组(n=92)和OSCC组(n=88),以40名口腔黏膜组织正常的健康志愿者为对照组。以人舌鳞癌细胞SCC9和人口腔角化细胞HOK为研究对象。采用qPCR检测miR-590在组织和细胞中的表达。用小干扰(si)-miR-590和si- nc质粒转染SCC9细胞。MTT法、流式细胞术和Transwell法分别检测细胞增殖、凋亡、迁移和侵袭能力。Western blotting检测细胞凋亡、迁移和侵袭相关蛋白的表达水平。对照组、OLP组和OSCC组miR-590的表达依次升高,提示其表达与OSCC患者TNM分期及淋巴结转移有关(P<0.05)。转染si-miR-590后,SCC9细胞的增殖、迁移和侵袭能力明显减弱,凋亡率升高(P<0.05)。Bcl-2、N-cadherin、vimentin表达量显著降低,Bax、E-cadherin表达量显著升高(P<0.05)。MiR-590在OSCC和SCC9细胞中高表达。沉默miR-590可抑制SCC9细胞的增殖、迁移和侵袭,促进SCC9细胞凋亡。
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来源期刊
Journal of Hard Tissue Biology
Journal of Hard Tissue Biology ENGINEERING, BIOMEDICAL-
CiteScore
0.90
自引率
0.00%
发文量
28
审稿时长
6-12 weeks
期刊介绍: Information not localized
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