| Literature DB >> 28588717 |
Guo-Hui Nie1, Zhao Li2,3, Hong-Fang Duan4, Liang Luo2,3, Hong-Yi Hu2, Wei-Qiang Yang2, Li-Ping Nie5, Ru-Fei Zhu2, Xiao-Fan Chen6, Wei Zhang6.
Abstract
The mechanism of nasopharyngeal carcinoma (NPC) remains unclear. The present study investigated the abnormal expression of long non-coding (lnc)RNAs in NPC tissues and one NPC cell line to identify the involvement of lncRNAs in the tumorigenesis of NPC. Using a quantitative reverse transcription polymerase chain reaction (RT-qPCR), the expression of lncRNA C22orf32-1 in NPC tissues and an NPC cell line was verified. The effects of lncRNA C22orf32-1 on NPC cells were investigated with a cell proliferation assay, cell scratch assay, Transwell assay and a cell apoptosis assay. The expression levels of lncRNA C22orf32-1 in NPC tissues and an NPC cell line were upregulated. lncRNA C22orf32-1 promoted the proliferation, migration and invasion of NPC cells, and reduced the apoptosis of NPC cells. The data demonstrated that lncRNA C22orf32-1 may facilitate the tumorigenesis of NPC, and may be used for the early diagnosis and treatment of NPC.Entities:
Keywords: biomarker; lncRNA C22orf32-1; nasopharyngeal carcinoma; oncogene; tumorigenesis
Year: 2017 PMID: 28588717 PMCID: PMC5452930 DOI: 10.3892/ol.2017.6021
Source DB: PubMed Journal: Oncol Lett ISSN: 1792-1074 Impact factor: 2.967