A novel risk signature that combines 10 long noncoding RNAs to predict neuroblastoma prognosis

J Cell Physiol. 2020 Apr;235(4):3823-3834. doi: 10.1002/jcp.29277. Epub 2019 Oct 14.

Abstract

Neuroblastoma (NBL) is the most frequently encountered extracranial solid neoplasm and impacts significantly on the survival of patients, especially in cases of advanced tumor stage or relapse. A long noncoding RNA (lncRNA) signature to predict the survival of patients with NBL is proposed in this paper. Differentially expressed lncRNA (DElncRNA) was selected using the Limma plus Voom package in R based on the RNA-sequencing data downloaded from the Therapeutically Applicable Research To Generate Effective Treatments database and Genotype-Tissue Expression database. Univariate cox regression analysis, least absolute shrinkage and selection operator regression analysis, and multivariate cox regression analysis were conducted to identify candidate DElncRNAs for the risk signature. Consequently, 10 DElncRNAs were designated as candidate DElncRNAs for the risk signature. Time-dependent receiver operating characteristic curves and Kapan-Meier survival curves confirmed the efficacy of the risk signature in predicting the survival of patients with NBL (area under the curve = 0.941; p ≤ .001). One of the DElncRNA constituent subparts (LINC01010) was significantly associated with the survival outcome of patients with NBL in GSE62564 (p = .004). Thus, a risk signature comprising 10 DElncRNAs was identified as effective for individual risk stratification and the survival prediction outcomes of patients with NBL.

Keywords: Therapeutically Applicable Research to Generate Effective Treatments; long noncoding RNA; neuroblastoma; prognosis; risk signature.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomarkers, Tumor / genetics*
  • Female
  • Gene Expression Regulation, Neoplastic / genetics
  • Humans
  • Infant
  • Kaplan-Meier Estimate
  • Male
  • Neoplasm Recurrence, Local / genetics*
  • Neoplasm Recurrence, Local / pathology
  • Neuroblastoma / genetics*
  • Neuroblastoma / pathology
  • Prognosis
  • RNA, Long Noncoding / classification
  • RNA, Long Noncoding / genetics*
  • Risk Factors
  • Sequence Analysis, RNA
  • Transcriptome

Substances

  • Biomarkers, Tumor
  • RNA, Long Noncoding