YY1-induced upregulation of FOXP4-AS1 and FOXP4 promote the proliferation of esophageal squamous cell carcinoma cells

Cell Biol Int. 2020 Jul;44(7):1447-1457. doi: 10.1002/cbin.11338. Epub 2020 Apr 20.

Abstract

Esophageal squamous cell carcinoma (ESCC) belongs to one of the most common malignant tumors worldwide and possesses high mortality. Long non-coding RNAs (lncRNAs) have been demonstrated to be essential biological participants in the progression of ESCC. On the basis of bio-informatics prediction, forkhead box P4 antisense RNA 1 (FOXP4-AS1) and forkhead box P4 (FOXP4) were upregulated in esophageal carcinoma samples and were positively correlated with each other. The present study aimed to explore the function of FOXP4-AS1 and FOXP4 in ESCC cells. Function assays disclosed that knockdown of FOXP4-AS1 or FOXP4 efficiently suppressed cell proliferation and induced cell apoptosis. Moreover, FOXP4-AS1 positively regulated FOXP4 by interacting with insulin-like growth factor 2 mRNA-binding protein 2 (IGF2BP2) to stabilize FOXP4 messenger RNA. In addition, FOXP4-AS1 could upregulate the expression of FOXP4 by sponging miR-3184-5p. Finally, we found that Yin Yang 1 (YY1) is a transcription factor that can transcriptionally activate both FOXP4-AS1 and FOXP4 in ESCC cells. In a word, YY1-induced upregulation of FOXP4-AS1 and FOXP4 promote the proliferation of ESCC cells.

Keywords: ESCC; FOXP4; FOXP4-AS1; IGF2BP2; proliferation.

MeSH terms

  • Cell Line, Tumor
  • Cell Proliferation / genetics*
  • Esophageal Neoplasms / genetics
  • Esophageal Neoplasms / pathology*
  • Esophageal Squamous Cell Carcinoma / genetics
  • Esophageal Squamous Cell Carcinoma / pathology
  • Forkhead Transcription Factors / genetics*
  • Gene Expression Regulation, Neoplastic / genetics*
  • Head and Neck Neoplasms / genetics
  • Humans
  • Mouth Neoplasms / genetics
  • RNA, Antisense / genetics
  • RNA, Long Noncoding / genetics
  • Squamous Cell Carcinoma of Head and Neck / genetics
  • Up-Regulation
  • YY1 Transcription Factor / genetics*
  • YY1 Transcription Factor / metabolism

Substances

  • FOXP4 protein, human
  • Forkhead Transcription Factors
  • RNA, Antisense
  • RNA, Long Noncoding
  • YY1 Transcription Factor
  • YY1 protein, human