Zhang Min, Dong Bing-Bin, Lu Min, Zheng Mei-Juan, Chen He, Ding Jing-Zhen, Xu A-Man, Xu Yuan-Hong
Clinical Laboratory, The First Affiliated Hospital of Anhui Medical University, Hefei, People's Republic of China.
Department of General Surgery, The First Affiliated Hospital of Anhui Medical University, Hefei, People's Republic of China.
Onco Targets Ther. 2016 Mar 3;9:1123-33. doi: 10.2147/OTT.S91879. eCollection 2016.
It has been previously reported that the deregulation of microRNAs in gastric cancer (GC) was correlated with the progression and prognosis. miR-429, a member of the miR-200 family, was previously shown to play an important role in human carcinomas. Our study shows that miR-429 is significantly downregulated in GC tissues compared with matched nontumor tissues. Overexpression of miR-429 in GC cells suppressed cell proliferation. Fascin-1 (FSCN1) was identified as one of the targets of miR-429 and knockdown of FSCN1 mimics the function of miR-429 overexpression. In conclusion, miR-429 acts as a tumor suppressor by targeting FSCN1, suggesting that miR-429 and FSCN1 can both be potential therapeutic targets of GC.
此前已有报道称,胃癌(GC)中微小RNA的失调与疾病进展和预后相关。miR-429是miR-200家族的成员之一,先前已证明其在人类癌症中发挥重要作用。我们的研究表明,与配对的非肿瘤组织相比,miR-429在GC组织中显著下调。GC细胞中miR-429的过表达抑制了细胞增殖。Fascin-1(FSCN1)被确定为miR-429的靶标之一,敲低FSCN1可模拟miR-429过表达的功能。总之,miR-429通过靶向FSCN1发挥肿瘤抑制作用,这表明miR-429和FSCN1都可能是GC的潜在治疗靶点。