Lu Yaoyong, Li Tao, Wei Ganbao, Liu Liangbo, Chen Qinsheng, Xu Lufei, Zhang Kunqiang, Zeng Dehao, Liao Rongwei
Department of Radiation Oncology, Gaozhou People's Hospital, Gaozhou, China.
Department of Cancer Chemotherapy, Gaozhou People's Hospital, Gaozhou, China.
Tumour Biol. 2016 Sep;37(9):11733-11741. doi: 10.1007/s13277-015-4773-4. Epub 2016 Mar 28.
Long non-coding RNAs (lncRNAs) play a critical role in cancer progression, including in nasopharyngeal carcinoma (NPC). However, it is still poorly understood whether lncRNA regulates epithelial to mesenchymal transition (EMT) and radioresistance of NPC cells. We found that lncRNA NEAT1 was significantly upregulated in NPC cell lines and tissues. Knockdown of NEAT1 could sensitize NPC cells to radiation in vitro. Further investigation found that NEAT1 regulated radioresistance by modulating EMT phenotype. Furthermore, we found that there was reciprocal repression between NEAT1 and miR-204. ZEB1 was identified as a downstream target of miR-204 and NEAT1 upregulated ZEB1 expression by negatively regulating miR-204 expression. Taking together, we proposed that NEAT1 regulated EMT phenotype and radioresistance by modulating the miR-204/ZEB1 axis in NPC.
长链非编码RNA(lncRNAs)在癌症进展中发挥关键作用,包括在鼻咽癌(NPC)中。然而,lncRNA是否调节NPC细胞的上皮-间质转化(EMT)和放射抗性仍知之甚少。我们发现lncRNA NEAT1在NPC细胞系和组织中显著上调。敲低NEAT1可使NPC细胞在体外对辐射敏感。进一步研究发现,NEAT1通过调节EMT表型来调节放射抗性。此外,我们发现NEAT1与miR-204之间存在相互抑制。ZEB1被鉴定为miR-204的下游靶点,NEAT1通过负调节miR-204表达上调ZEB1表达。综上所述,我们提出NEAT1通过调节NPC中的miR-204/ZEB1轴来调节EMT表型和放射抗性。