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Upregulated long-non-coding RNA DLEU2 exon 9 expression was an independent indicator of unfavorable overall survival in patients with esophageal adenocarcinoma.
Ma, Wen; Zhang, Chang-Qing; Dang, Cheng-Xue; Cai, Hong-Yi; Li, Hong-Ling; Miao, Guo-Ying; Wang, Jian-Kai; Zhang, Li-Juan.
Affiliation
  • Ma W; Department of Surgical Oncology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, 710000, China; Department of Radiotherapy, Gansu Province Hospital, Lanzhou, 730000, China.
  • Zhang CQ; Department of Tumor Center, Gansu Province Hospital, Lanzhou, 730000, China.
  • Dang CX; Department of Surgical Oncology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, 710000, China. Electronic address: dangchengxue@mail.xjtu.edu.cn.
  • Cai HY; Department of Radiotherapy, Gansu Province Hospital, Lanzhou, 730000, China.
  • Li HL; Department of Tumor Center, Gansu Province Hospital, Lanzhou, 730000, China.
  • Miao GY; Department of Radiotherapy, Gansu Province Hospital, Lanzhou, 730000, China.
  • Wang JK; Department of Radiotherapy, Gansu Province Hospital, Lanzhou, 730000, China.
  • Zhang LJ; Department of Radiotherapy, Gansu Province Hospital, Lanzhou, 730000, China.
Biomed Pharmacother ; 113: 108655, 2019 May.
Article in En | MEDLINE | ID: mdl-30849637
In this study, we aimed to explore the expression profiles of some known functional lncRNAs in esophageal adenocarcinoma (EAD) and to screening the potential prognostic makers, using data from The Cancer Genome Atlas (TCGA)-esophageal carcinoma (ESCA). Results showed that DLEU2 is a high potential OS related marker among 73 functional lncRNAs. DLEU2 and its intronic miR-15a and miR-16-1 expression were significantly upregulated in EAD compared with adjacent normal tissues. However, miR-15a and miR-16-1 expression were only weakly correlated with DLEU2 expression. Univariate and multivariate analysis confirmed that DLEU2 expression, but not miR-15a or miR-16-1 expression is an independent prognostic marker in terms of OS (HR:1.688, 95%CI: 1.085-2.627, p = 0.020) in EAD patients. The exon 9 of DLEU2 is very strongly co-expressed with DLEU2 (Pearson's r = 0.96) and showed better predictive value than total DLEU2 expression in predicting the OS of EAD patients. Multivariate analysis confirmed its independent prognostic value (HR:1.970, 95%CI: 1.266-3.067, p = 0.003), after adjustment of histologic grade, pathological stages and the presence of residual tumor. By checking the methylation status of DLEU2 gene, we excluded the possibility of the influence of two CpG sites near the DLEU2 exon 9 locus on its expression. In addition, although copy number alterations (CNAs) were observed DLEU2 gene, heterozygous loss (-1), low-level copy gain (+1) and high-level amplification (+2) had no significant association with DLEU2 transcription. Based on these findings, we infer that DLEU2 exon 9 expression might serve as a valuable biomarker of unfavorable OS in EAD patients.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Esophageal Neoplasms / Adenocarcinoma / Biomarkers, Tumor / Exons / Tumor Suppressor Proteins / RNA, Long Noncoding Type of study: Prognostic_studies Limits: Female / Humans / Male Language: En Journal: Biomed Pharmacother Year: 2019 Type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Esophageal Neoplasms / Adenocarcinoma / Biomarkers, Tumor / Exons / Tumor Suppressor Proteins / RNA, Long Noncoding Type of study: Prognostic_studies Limits: Female / Humans / Male Language: En Journal: Biomed Pharmacother Year: 2019 Type: Article Affiliation country: China