The long noncoding RNA-ROR promotes the resistance of radiotherapy for human colorectal cancer cells by targeting the p53/miR-145 pathway

J Gastroenterol Hepatol. 2017 Apr;32(4):837-845. doi: 10.1111/jgh.13606.

Abstract

Background and aim: Long intergenic noncoding RNAs (lincRNAs) have critical roles in elevating efficacy of anticancer therapy and tumor progression. Recent studies show that Regulator of Reprogramming (ROR) is aberrantly expressed in several types of cancer, including colorectal cancer (CRC). Radiotherapy is considered as a standard preoperative treatment. However, a considerable number of CRCs are resistant to radiotherapy. In this study, we evaluated the role of lincRNA-ROR in radiotherapy for CRC and detected the underlying molecular mechanism.

Methods: Real-time polymerase chain reaction was employed to quantify the expression level of lincRNA-ROR in different CRC cell lines and tissue samples. Cell viability and apoptosis assays were used to confirm the radiotherapy-mediated effects by lincRNA-ROR altered expression. The direct impact of lincRNA-ROR on the expression of p53/miR-145 by loss-of-function and gain-of-function strategy was also analyzed. A xenograft mouse model was used to evaluate the role of linc-ROR in CRC treatment.

Results: We discovered that lincRNA-ROR was upregulated in CRC cell lines and tissue samples. We further showed that knockdown of lincRNA-ROR enhanced the sensitivity to radiotherapy for CRC by inhibiting cell viability and promoting apoptosis. Activity of the p53/miR-145 pathway may help explain the role of lincRNA-ROR for stress-induced regulation in CRC therapy. Combined specific knockdown of lincRNA-ROR and radiotherapy treatment in xenograft model resulted in a significant reduction in the tumor growth.

Conclusion: LincRNA-ROR decreases sensitivity to radiotherapy via the negative regulation of p53/miR-145 and may represent a potential target for the treatment of CRC.

Keywords: colorectal cancer; combined treatment; lincRNA-ROR; p53/miR-145 pathway; radiotherapy.

MeSH terms

  • Animals
  • Apoptosis
  • Cell Survival
  • Colorectal Neoplasms / genetics*
  • Colorectal Neoplasms / pathology
  • Colorectal Neoplasms / radiotherapy*
  • Disease Models, Animal
  • Gene Expression
  • Humans
  • Male
  • Mice, Nude
  • MicroRNAs / physiology*
  • Molecular Targeted Therapy*
  • Neoplasm Transplantation
  • RNA, Long Noncoding / physiology*
  • RNA, Untranslated / physiology*
  • Real-Time Polymerase Chain Reaction
  • Signal Transduction / physiology*
  • Tumor Suppressor Protein p53 / physiology*
  • Up-Regulation

Substances

  • MIRN145 microRNA, human
  • MIRN145a microRNA, mouse
  • MicroRNAs
  • RNA, Long Noncoding
  • RNA, Untranslated
  • Tumor Suppressor Protein p53