Oncotarget

Meta-Analysis:

Prognostic value of long noncoding RNA ZFAS1 in various carcinomas: a meta-analysis

Dan Dong, Zhongyi Mu, Wei Wang, Na Xin, Xiaowen Song, Yue Shao and Chenghai Zhao _

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Oncotarget. 2017; 8:84497-84505. https://doi.org/10.18632/oncotarget.21100

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Abstract

Dan Dong1,*, Zhongyi Mu1,2,*, Wei Wang1, Na Xin1, Xiaowen Song1, Yue Shao1 and Chenghai Zhao1

1Department of Pathophysiology, College of Basic Medical Science, China Medical University, Shenyang, People’s Republic of China

2Department of Urology, Cancer Hospital of China Medical University, Liaoning Cancer Hospital and Institute, Shenyang, People’s Republic of China

*These authors contributed equally to this work

Correspondence to:

Chenghai Zhao, email: [email protected]

Keywords: zinc finger antisense 1, long noncoding RNA, prognosis, meta-analysis

Received: May 07, 2017     Accepted: August 28, 2017     Published: September 20, 2017

ABSTRACT

A number of studies have revealed that zinc finger antisense 1 (ZFAS1), a long noncoding RNA (lncRNA), is aberrantly regulated in various cancers, and high ZFAS1 expression is associated with poor prognosis and increased risk of lymph node metastasis (LNM). This meta-analysis was conducted to identify the potential value of ZFAS1 as a biomarker for cancer prognosis. We searched electronic database PubMed, Web of Science, and China Wanfang Data (up to June 1, 2017) to collect all relevant studies and explore the association of ZFAS1 expression with overall survival (OS) and LNM. The results showed that cancer patients with high ZFAS1 expression had a worse OS than those with low ZFAS1 expression (HR: 1.94, 95% confidence interval [CI]: 1.41–2.47, P < 0.001), and high ZFAS1 expression was significantly associated with LNM (OR: 2.60, 95% CI: 1.54–4.42, P < 0.001). Subgroup analysis revealed that high ZFAS1 expression was significantly related to high incidence of LNM in subgroups of sample size more than 88 (OR: 3.16, 95% CI: 2.06–4.86, P < 0.001), non-digestive system malignancies (OR: 4.05, 95% CI: 2.49–6.60, P < 0.001), and studies reported in 2017 (OR: 4.86, 95% CI: 2.67–8.84, P < 0.001) without significant heterogeneity. Further meta-regression by the covariates showed that tumor type, sample size, quality score, cut off value and publication year did not result in the inter-study heterogeneity. In conclusion, the present meta-analysis demonstrates that high ZFAS1 expression may potentially serve as a reliable biomarker for poor clinical outcome in various cancers.


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