Genome-wide profiling of long non-coding RNA expression patterns in the EGFR-TKI resistance of lung adenocarcinoma by microarray

Oncol Rep. 2016 Jun;35(6):3371-86. doi: 10.3892/or.2016.4758. Epub 2016 Apr 20.

Abstract

Mutations in the epidermal growth factor receptor (EGFR) make lung adenocarcinoma cells sensitive to EGFR tyrosine kinase inhibitors (TKIs). Long-term cancer therapy may cause the occurrence of acquired resistance to EGFR TKIs. Long non-coding RNAs (lncRNAs) play important roles in tumor formation, tumor metastasis and the development of EGFR-TKI resistance in lung cancer. To gain insight into the molecular mechanisms of EGFR-TKI resistance, we generated an EGFR-TKI-resistant HCC827-8-1 cell line and analyzed expression patterns by lncRNA microarray and compared it with its parental HCC827 cell line. A total of 1,476 lncRNA transcripts and 1,026 mRNA transcripts were dysregulated in the HCC827‑8-1 cells. The expression levels of 7 chosen lncRNAs were validated by real-time quantitative PCR. As indicated by functional analysis, several groups of lncRNAs may be involved in the bio-pathways associated with EGFR-TKI resistance through their cis- and/or trans‑regulation of protein-coding genes. Thus, lncRNAs may be used as novel candidate biomarkers and potential targets in EGFR-TKI therapy in the future.

MeSH terms

  • Adenocarcinoma / drug therapy*
  • Adenocarcinoma / genetics
  • Adenocarcinoma of Lung
  • Cell Line, Tumor
  • Drug Resistance, Neoplasm
  • E2F1 Transcription Factor / physiology
  • ErbB Receptors / antagonists & inhibitors*
  • Humans
  • Lung Neoplasms / drug therapy*
  • Lung Neoplasms / genetics
  • MicroRNAs / analysis
  • Oligonucleotide Array Sequence Analysis
  • Protein Kinase Inhibitors / therapeutic use*
  • RNA, Long Noncoding / analysis*
  • Real-Time Polymerase Chain Reaction
  • Upstream Stimulatory Factors / physiology

Substances

  • E2F1 Transcription Factor
  • E2F1 protein, human
  • MicroRNAs
  • Protein Kinase Inhibitors
  • RNA, Long Noncoding
  • USF1 protein, human
  • Upstream Stimulatory Factors
  • EGFR protein, human
  • ErbB Receptors