Liu Jianchao, Du Wenfeng
Department of Gastroenterological Surgery, Liaocheng People's Hospital, Liaocheng Clinical School of Taishan Medical University, Liaocheng, Shandong Province, 252000, People's Republic of China.
Onco Targets Ther. 2019 May 30;12:4287-4295. doi: 10.2147/OTT.S195853. eCollection 2019.
Homo sapiens FOXF1 adjacent noncoding developmental regulatory RNA (FENDRR) is a novel long noncoding RNA (lncRNA) exerting important effects on transcriptional and post-transcriptional regulation. The purpose of this study was to investigate the potential role of FENDRR in colon cancer. Multiple cellular and molecular biology experiments were performed in the present study, such as CCK-8, Western blot, immunohistochemistry, confocal immunofluorescent and animal studies. We determined that attenuation of FENDRR was a frequent event in colon cancer tissues and colon cancer cell lines, in contrast to their normal counterparts. Low levels of FENDRR were associated with the clinical stages and poor prognosis. Moreover, ectopic expression of FENDRR repressed colon cancer cell viability, invasion and epithelial-mesenchymal transition. Furthermore, through a series of in vitro and in vivo assays, we reported the discovery of FENDRR modulating the expression of SOX4 protein, and hence in the progression of colon cancer. Based on these data, we demonstrated that FENDRR may function as a tumor-suppressor gene by repressing SOX4 and as a potential therapeutic target for colon cancer.
人类FOXF1相邻非编码发育调控RNA(FENDRR)是一种新型长链非编码RNA(lncRNA),对转录和转录后调控发挥重要作用。本研究旨在探讨FENDRR在结肠癌中的潜在作用。本研究进行了多项细胞和分子生物学实验,如CCK-8、蛋白质印迹、免疫组织化学、共聚焦免疫荧光和动物研究。我们确定,与正常组织相比,FENDRR表达减弱在结肠癌组织和结肠癌细胞系中是常见现象。低水平的FENDRR与临床分期及预后不良相关。此外,FENDRR的异位表达抑制结肠癌细胞的活力、侵袭和上皮-间质转化。此外,通过一系列体外和体内实验,我们发现FENDRR可调节SOX4蛋白的表达,进而影响结肠癌的进展。基于这些数据,我们证明FENDRR可能通过抑制SOX4发挥肿瘤抑制基因的作用,并可能成为结肠癌的潜在治疗靶点。