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Expression and Clinical Significance of the Novel Long Noncoding RNA ZNF674-AS1 in Human Hepatocellular Carcinoma

Authors :
Lin Zhou
Dongkai Zhou
Tianyu He
Yuan Zhang
Weilin Wang
Minjie Xie
Yang Kong
Qiang Sun
Haiyang Xie
Shusen Zheng
Yingcai Yan
Lufei Zhang
Pengfei Huang
Xiaohu Zhou
Linshi Zhang
Source :
BioMed Research International, BioMed Research International, Vol 2016 (2016)
Publication Year :
2016
Publisher :
Hindawi Publishing Corporation, 2016.

Abstract

Long noncoding RNAs (lncRNAs) play crucial roles in cancer occurrence and progression. However, the relationship between the expression levels of lncRNAs and the hepatocellular carcinoma (HCC) process is unclear. The goal of this study was to determine the expression level of ZNF674-AS1, a newly found lncRNA, in HCC and its clinical association. The expression of ZNF674-AS1 in 137 pairs of tumorous and adjacent normal tissues from patients with HCC was detected by quantitative real-time reverse transcription polymerase chain reaction. Additionally, the potential associations between its level in HCC tissue and clinicopathological features were analyzed. The expression of ZNF674-AS1 in the HCC cell lines HepG2, HCCLM3, SK-Hep1, HuH7, Hep3B, and MHCC97H was significantly downregulated compared with that in the normal liver cell line QSG-7701. The expression of ZNF674-AS1 was downregulated in 72% (99/137) of HCC tissues compared with that in paired adjacent normal tissues (p<0.01). The results showed that the ZNF674-AS1 expression level was significantly correlated with metastasis (p=0.041), clinical stage (p=0.039), and histopathologic grading (p=0.045). In addition, the Kaplan–Meier survival curves revealed that low ZNF674-AS1 expression was associated with poor prognosis in patients with HCC. Our data suggest that ZNF674-AS1 may play some role during cancer occurrence and progression and may be a new biomarker for HCC.

Details

Language :
English
ISSN :
23146141 and 23146133
Volume :
2016
Database :
OpenAIRE
Journal :
BioMed Research International
Accession number :
edsair.doi.dedup.....76c1ee282ac1242371229a377d845e48