LncRNAAC132217.4, a KLF8-regulated long non-coding RNA, facilitates oral squamous cell carcinoma metastasis by upregulating IGF2 expression

Cancer Lett. 2017 Oct 28:407:45-56. doi: 10.1016/j.canlet.2017.08.007. Epub 2017 Aug 18.

Abstract

Increasing evidence has revealed the aberrant expression of long non-coding RNAs (lncRNAs) in many cancer types, including oral squamous cell carcinoma (OSCC). However, limited investigations report metastasis-related lncRNAs in OSCC. Herein, we report the identification of dysregulated intergenic lncRNAs in the highly metastatic OSCC cell line, UM-SCC6H. One of the lncRNAs, termed AC132217.4, was remarkably upregulated and promoted cell migration and epithelial-mesenchymal transition (EMT) by upregulating IGF2 expression. Further mechanistic studies revealed that AC132217.4 interacted with the 3'UTR of IGF2 mRNA and increased its stability, leading to increased IGF2 levels. Thereafter, we found that KLF8 binds to the upstream sequence of AC132217.4, activating its expression at the transcriptional level, which accelerated OSCC metastasis via the AC132217.4-IGF2 axis both in vitro and in vivo. We also revealed that the expression level of AC132217.4 was increased in OSCC tissues, and this elevation correlated with KLF8 and IGF2 expression. Thus, our data demonstrate that the KLF8-AC132217.4-IGF2 signalling pathway plays a critical role in OSCC metastasis.

Keywords: Cell meatastasis; IGF2; KLF8; LncRNAs; Oral squamous cell carcinoma.

MeSH terms

  • Carcinoma, Squamous Cell / metabolism*
  • Carcinoma, Squamous Cell / secondary*
  • Cell Line, Tumor
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Insulin-Like Growth Factor II / metabolism*
  • Kruppel-Like Transcription Factors
  • Mouth Neoplasms / metabolism*
  • Mouth Neoplasms / pathology*
  • Neoplasm Metastasis
  • Neoplasm Proteins / metabolism
  • Neoplasm Proteins / physiology*
  • RNA, Long Noncoding / metabolism
  • RNA, Long Noncoding / physiology*
  • RNA, Messenger / metabolism
  • Repressor Proteins / metabolism
  • Repressor Proteins / physiology*
  • Up-Regulation

Substances

  • AC132217.4 long noncoding RNA, human
  • IGF2 protein, human
  • KLF8 protein, human
  • Kruppel-Like Transcription Factors
  • Neoplasm Proteins
  • RNA, Long Noncoding
  • RNA, Messenger
  • Repressor Proteins
  • Insulin-Like Growth Factor II