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Article type: Research Article
Authors: Bao, Jiea | Zhou, Chenjieb | Zhang, Jiaqingc | Mo, Jiaqiangd | Ye, Qingd | He, Junmingd | Diao, Jingfangd; *
Affiliations: [a] Department of Internal Medicine, Hospital of South China Normal University, Guangzhou 510631, Guangdong, China | [b] Department of Hepatic Surgery, Zhujiang Hospital of Southern Medical University, Guangzhou, Guangdong, China | [c] Department of Cardiothoracic Surgery, Zhujiang Hospital of Southern Medical University, Guangzhou, Guangdong, China | [d] Department of Hepatobiliary Surgery, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine (Guangdong Provincial Hospital of TCM), Guangzhou 510120, Guangdong, China
Correspondence: [*] Corresponding author: Jingfang Diao, Department of Hepatobiliary Surgery, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine (Guangdong Provincial Hospital of TCM), Guangzhou 510120, Guangdong, China. Tel.: +86 20 81887233 ext 33329; Fax: +86 20 81887233 ext 33330; E-mail: [email protected].
Abstract: BACKGROUND: The long non-coding RNA FOXD2-AS1 is highly expressed in non-small cell lung cancer and promotes malignant progression. However, the role of FOXD2-AS1 in esophageal squamous cell carcinoma (ESCC) is still unclear. OBJECTIVE: In this study, we examined the relationships between the expression level of FOXD2-AS1 and the outcome of ESCC patients. METHODS: Expression of FOXD2-AS1 was evaluated in cancer tissue and adjacent non-tumor tissue samples from 147 ESCC patients who received radical surgical resection using qRT-PCR. The correlations between the expression level of FOXD2-AS1 and patients’ overall (OS) and disease free survival (DFS) were analyzed. RESULTS: FOXD2-AS1 expression was upregulated in ESCC tissue than that in adjacent non-tumor tissue samples (P< 0.001). Kaplan-Meier analysis showed that high FOXD2-AS1 expression was correlated with poor prognosis in ESCC patients. Patients with a high level of FOXD2-AS1 had a shorter OS and DFS than those with a low level of FOXD2-AS1 (P= 0.005 and 0.0001, respectively). On multivariate analysis, the hazard ratio of FOXD2-AS1 expression was 1.66 (95% CI = 1.04–2.64, P= 0.033) for OS and 2.68 (95% CI = 1.49–4.82, P= 0.001) for DFS. CONCLUSIONS: Overall, our results provided convinced evidence that FOXD2-AS1 may serve as a predictive marker for ESCC patients’ survival.
Keywords: Long non-coding RNA, FOXD2-AS1, survival, esophageal squamous cell carcinoma
DOI: 10.3233/CBM-170260
Journal: Cancer Biomarkers, vol. 21, no. 3, pp. 527-533, 2018
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