Xiong Jing, Liu Ying, Luo Shengjun, Jiang Li, Zeng Yang, Chen Zhixiong, Shi Xiaobo, Lv Bufan, Tang Wei
Department of Urology, The First Affiliated Hospital of Chongqing Medical University, Chongqing.
Department of Urology and Andrology, Taihe Hospital, Hubei University of Medicine, Shiyan, Hubei Province, China.
Oncotarget. 2017 Jan 24;8(4):6555-6563. doi: 10.18632/oncotarget.14149.
Increasing evidence indicates that long non-coding RNAs (lncRNAs) have been associated with cancer development. However, the contributions of lncRNAs to renal cell carcinoma (RCC) remain poorly characterized. Here, we identified a novel lncRNA, termed HEIRCC, which was up-regulated in RCC tissues through lncRNA microarray analysis and subsequent validation in 60 RCC clinical specimens and cell lines. The high expression of HEIRCC is associated closely with the clinical pathology features such as larger tumor size, poor differentiation, lymphatic metastasis. In vitro assays revealed that HEIRCC knockdown could inhibit cell proliferation, trigger late apoptosis, suppress cell migration and invasion. We further demonstrated that depletion of HEIRCC reduce the epithelial to mesenchymal transition (EMT) program by regulating expression levels of EMT-associated markers in RCC cells. Thus, HEIRCC might be act as an important regulator of EMT in RCC progression and might be a novel therapeutic target for the advanced RCC therapy.
越来越多的证据表明,长链非编码RNA(lncRNAs)与癌症发展有关。然而,lncRNAs对肾细胞癌(RCC)的作用仍不清楚。在此,我们鉴定出一种名为HEIRCC的新型lncRNA,通过lncRNA微阵列分析以及随后在60例RCC临床标本和细胞系中的验证,发现其在RCC组织中上调。HEIRCC的高表达与较大肿瘤大小、低分化、淋巴转移等临床病理特征密切相关。体外实验表明,敲低HEIRCC可抑制细胞增殖,引发晚期凋亡,抑制细胞迁移和侵袭。我们进一步证明,HEIRCC的缺失通过调节RCC细胞中EMT相关标志物的表达水平来减少上皮-间质转化(EMT)程序。因此,HEIRCC可能是RCC进展中EMT的重要调节因子,可能是晚期RCC治疗的新靶点。