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在食管鳞状细胞癌中,微小RNA-375通过直接靶向短 stature homeobox 2(SHOX2)抑制侵袭和转移。

MiR-375 suppresses invasion and metastasis by direct targeting of SHOX2 in esophageal squamous cell carcinoma.

作者信息

Yi Jun, Jin Li, Chen Jing, Feng Bing, He Zhenyue, Chen Longbang, Song Haizhu

机构信息

Department of Cardiothoracic Surgery, Jinling Hospital, Nanjing 210002, China.

Department of Medical Oncology, Jinling Hospital, Nanjing 210002, China.

出版信息

Acta Biochim Biophys Sin (Shanghai). 2017 Feb 6;49(2):159-169. doi: 10.1093/abbs/gmw131.

Abstract

Esophageal squamous cell carcinoma (ESCC) is the most common histological type in China. MicroRNAs are endogenously expressed in mammals and play a significant role in tumor invasion and metastasis by targeting potential downstream genes. In the present study, microarray analysis showed that miR-375 expression was distinctly downregulated in ESCC compared with that in normal esophageal epithelium tissues. Then, luciferase reporter assay showed that SHOX2 was the direct downstream target of miR-375 and this interaction was confirmed by the rescue experiments. Quantitative polymerase chain reaction results also showed that SHOX2 expression was upregulated in ESCC cells and tissues. Further analysis showed that SHOX2 induced proliferation, invasion, and metastasis of ESCC both in vivo and in vitro. Moreover, the interaction between miR-375 and SHOX2 affected the epithelial-to-mesenchymal transition. We conclude that miR-375 may suppress invasion and metastasis of ESCC by directly targeting SHOX2. The miR-375/SHOX2 axis may be a novel therapeutic target for ESCC.

摘要

食管鳞状细胞癌(ESCC)是中国最常见的组织学类型。微小RNA在哺乳动物体内内源性表达,通过靶向潜在的下游基因在肿瘤侵袭和转移中发挥重要作用。在本研究中,微阵列分析表明,与正常食管上皮组织相比,ESCC中miR-375的表达明显下调。然后,荧光素酶报告基因检测表明SHOX2是miR-375的直接下游靶点,并且这种相互作用通过挽救实验得到证实。定量聚合酶链反应结果还表明,ESCC细胞和组织中SHOX2的表达上调。进一步分析表明,SHOX2在体内和体外均诱导ESCC的增殖、侵袭和转移。此外,miR-375与SHOX2之间的相互作用影响上皮-间质转化。我们得出结论,miR-375可能通过直接靶向SHOX2抑制ESCC的侵袭和转移。miR-375/SHOX2轴可能是ESCC的一个新的治疗靶点。

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