Hu Changmei, Lv Liang, Peng Jie, Liu Deliang, Wang Xuehong, Zhou Yuqian, Huo Jirong
Department of Gastroenterology, The Second Xiangya Hospital of Central South University, Changsha, Hunan 410011, P.R. China.
Department of Haematology, Xiangya Hospital of Central South University, Changsha, Hunan 410078, P.R. China.
Oncol Lett. 2017 Jun;13(6):4769-4775. doi: 10.3892/ol.2017.6098. Epub 2017 Apr 26.
Accumulating evidence indicates that aberrant expression of microRNAs is involved in tumorigenesis, tumor progression and response to therapy. MicroRNA-375 (miR-375) is an important cancer-associated RNA that is downregulated in multiple types of cancer. In the present study, the potential effects of and underlying molecular mechanism for miR-375 in esophageal cancer were investigated. The expression of miR-375 in paired esophageal squamous cell carcinoma (ESCC) and non-tumor tissues from 10 patients was quantified using the reverse transcription-quantitative polymerase chain reaction. The miR-375 levels in the ESCC cell line EC109 and a normal esophageal epithelial cell line, Het-1A, were also detected. The effect of miR-375 on ESCC cell growth and invasion was determined using Cell Counting kit-8, flow cytometry and invasion assays. A luciferase assay was conducted for target identification. The results of the present study revealed that miR-375 was downregulated in ESCC tumor tissue and EC109 cells compared with normal tissue and Het-1A cells (P<0.01). Overexpression of miR-375 inhibited EC109 cell growth and invasion, and induced cell cycle arrest. In addition, metadherin (MTDH) was demonstrated to be a direct target of miR-375 (P<0.01). The overexpression of miR-375 downregulated MTDH (P<0.01), cyclin D1 (P<0.05) and vascular endothelial growth factor (P<0.01) expression, while upregulating epithelial cadherin (P<0.01) expression, which may account for its effect on ESCC cell proliferation and invasion. The results of the present study suggest that the miR-375/MTDH axis represents a target for the treatment of ESCC.
越来越多的证据表明,微小RNA的异常表达与肿瘤发生、肿瘤进展及治疗反应有关。微小RNA-375(miR-375)是一种重要的癌症相关RNA,在多种癌症中表达下调。在本研究中,对miR-375在食管癌中的潜在作用及潜在分子机制进行了研究。采用逆转录-定量聚合酶链反应对10例患者配对的食管鳞状细胞癌(ESCC)组织和非肿瘤组织中miR-375的表达进行定量。还检测了ESCC细胞系EC109和正常食管上皮细胞系Het-1A中miR-375的水平。使用细胞计数试剂盒-8、流式细胞术和侵袭实验确定miR-375对ESCC细胞生长和侵袭的影响。进行荧光素酶实验以鉴定靶点。本研究结果显示,与正常组织和Het-1A细胞相比,ESCC肿瘤组织和EC109细胞中miR-375表达下调(P<0.01)。miR-375过表达抑制EC109细胞生长和侵袭,并诱导细胞周期停滞。此外,证实黏附分子(MTDH)是miR-375的直接靶点(P<0.01)。miR-375过表达下调MTDH(P<0.01)、细胞周期蛋白D1(P<0.05)和血管内皮生长因子(P<0.01)的表达,同时上调上皮钙黏蛋白(P<0.01)的表达,这可能解释了其对ESCC细胞增殖和侵袭的影响。本研究结果表明,miR-375/MTDH轴是ESCC治疗的一个靶点。