SP1-induced AFAP1-AS1 contributes to proliferation and invasion by regulating miR-497-5p/CELF1 pathway in nasopharyngeal carcinoma

Hum Cell. 2021 Mar;34(2):491-501. doi: 10.1007/s13577-020-00475-y. Epub 2021 Jan 5.

Abstract

Nasopharyngeal carcinoma is a type of otolaryngological malignancy with high incidence. Long non-coding RNAs (lncRNAs) are closely related to nasopharyngeal carcinoma. LncRNA AFAP1-AS1 (AFAP1-AS1) has been found to play important roles in nasopharyngeal carcinoma progression and poor prognosis. However, the mechanism underlying AFAP1-AS1 in regulating nasopharyngeal carcinoma is still unclear. In current study, AFAP1-AS1 was found to be up-regulated in nasopharyngeal carcinoma tissues and cells. AFAP1-AS1 overexpression and knockdown were conducted in nasopharyngeal carcinoma cells. The results proved that AFAP1-AS1 promoted the survival and migration of nasopharyngeal carcinoma cells. Additionally, specificity protein 1 (SP1) was enhanced in nasopharyngeal carcinoma tissues and cells, and induced AFAP1-AS1 expression. The interaction between AFAP1-AS1 and miR-497-5p was confirmed. AFAP1-AS1 was demonstrated to regulate CELF1, a target gene of miR-497-5p. Further functional analysis revealed that AFAP1-AS1 knockdown attenuated SP1-induced nasopharyngeal carcinoma progression. These results indicate that SP1-induced AFAP1-AS1 facilitates nasopharyngeal carcinoma progression by regulating miR-497-5p/CELF1 pathway, which provides a new target for nasopharyngeal carcinoma treatment.

Keywords: AFAP1-AS1; Nasopharyngeal carcinoma; SP1; miR-497-5p.

MeSH terms

  • CELF1 Protein / metabolism*
  • Cell Line, Tumor
  • Cell Proliferation / genetics*
  • Gene Expression Regulation, Neoplastic / genetics*
  • Humans
  • MicroRNAs / metabolism*
  • Microfilament Proteins / physiology*
  • Molecular Targeted Therapy
  • Nasopharyngeal Carcinoma / genetics*
  • Nasopharyngeal Carcinoma / pathology*
  • Nasopharyngeal Neoplasms / genetics*
  • Nasopharyngeal Neoplasms / pathology*
  • Neoplasm Invasiveness / genetics*
  • RNA, Long Noncoding / physiology*
  • Signal Transduction / genetics*
  • Signal Transduction / physiology
  • Sp1 Transcription Factor / physiology*

Substances

  • AFAP1 protein, human
  • CELF1 Protein
  • CELF1 protein, human
  • MicroRNAs
  • Microfilament Proteins
  • RNA, Long Noncoding
  • Sp1 Transcription Factor
  • SP1 protein, human