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心肌细胞特异性增强子结合因子2D促进舌鳞状细胞癌的肿瘤发生与进展。

Myocyte-specific enhancer factor 2D promotes tumorigenesis and progression in tongue squamous cell carcinoma.

作者信息

Liu Yang, Yu Wenjun, Zhu Yan, Sun Zhenni, Huang Xingang, Zhou Jianhua, Yao Ruyong, Zhang Qian, Qiu Jianzhong, Yue Lu

机构信息

Department of Oncology, Qingdao Municipal Hospital Qingdao, China.

Department of Pathology, Qingdao Municipal Hospital Qingdao, China.

出版信息

Int J Clin Exp Pathol. 2020 May 1;13(5):934-943. eCollection 2020.

Abstract

Tongue squamous cell carcinoma (TSCC) ranks as one of the most common cancers worldwide and has a poor prognosis. Myocyte-specific enhancer factor 2 (MEF2D) has recently been considered as a novel factor involved in cancer development. In the present study, the function and underlying mechanism of MEF2D in TSCC were investigated. The levels of MEF2D mRNA and protein were determined in human TSCC samples by RT-qPCR and western blot, respectively. The interaction between MEF2D expression and clinicopathologic features was evaluated by IHC and analysis of clinical information. MEF2D-mediated effects on proliferation, migration, and invasion were explored in TSCC cells after transfection with MEF2D-siRNA. The results showed higher expression of MEF2D at both the mRNA and protein levels in TSCC carcinoma tissues than in paracarcinoma tissues. Furthermore, high expression of MEF2D was positively correlated with tumor differentiation and lymphatic metastasis. MEF2D knocked down TSCCA cells also had reduced proliferative, migratory, and invasive abilities compared to those of control cells. Together, these data confirmed that knockdown of MEF2D might suppress the growth and metastasis of TSCC, which further indicated that MEF2D might serve as a therapeutic target for TSCC treatment.

摘要

舌鳞状细胞癌(TSCC)是全球最常见的癌症之一,预后较差。肌细胞特异性增强因子2(MEF2D)最近被认为是参与癌症发展的一个新因子。在本研究中,对MEF2D在TSCC中的功能及潜在机制进行了研究。分别通过RT-qPCR和蛋白质印迹法测定人TSCC样本中MEF2D mRNA和蛋白质的水平。通过免疫组化和临床信息分析评估MEF2D表达与临床病理特征之间的相互作用。用MEF2D-siRNA转染TSCC细胞后,探讨MEF2D对细胞增殖、迁移和侵袭的影响。结果显示,TSCC癌组织中MEF2D的mRNA和蛋白质水平均高于癌旁组织。此外,MEF2D的高表达与肿瘤分化和淋巴转移呈正相关。与对照细胞相比,敲低MEF2D的TSCCA细胞的增殖、迁移和侵袭能力也降低。总之,这些数据证实敲低MEF2D可能抑制TSCC的生长和转移,这进一步表明MEF2D可能作为TSCC治疗的一个靶点。

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