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Downregulation of lncRNA APCDD1L-AS1 due to DNA hypermethylation and loss of VHL protein expression promotes the progression of clear cell renal cell carcinoma

Int J Biol Sci. 2022 Mar 21;18(6):2583-2596. doi: 10.7150/ijbs.71519. eCollection 2022.

Abstract

Background: The current studies only indicated that long non-coding RNA (lncRNA) APCDD1L-AS1, as a novel lncRNA, may play a role in oral squamous cell carcinoma and lung cancer. However, its potential role in clear cell renal cell carcinoma (ccRCC) and its possible mechanism of action remain vague. Methods: TCGA-KIRC and GEO data and qRT-PCR and pyrosequencing results of clinical specimens were used to identify the expression level and DNA methylation status of APCDD1L-AS1. The effects of APCDD1L-AS1 overexpression on ccRCC growth and metastasis were determined by function experiments. Western blot and Tandem mass tags (TMT) were utilized to explore the relationship between APCDD1L-AS1 and VHL expression and its downstream underlying mechanisms. Results: The expression of APCDD1L-AS1 was downregulated in ccRCC. Decreased APCDD1L-AS1 expression was related to higher tumor stage and histological grade and shorter RFS (Relapse-free survival). Besides, APCDD1L-AS1 overexpression restrained the growth and metastasis of ccRCC cells in vitro and in vivo. Moreover, reduced APCDD1L-AS1 expression could be caused by DNA hypermethylation and loss of von Hippel Lindau (VHL) protein expression. Furthermore, the dysregulation of histones expression caused by APCDD1L-AS1 overexpression may be one of the important mechanisms to suppress the progression of ccRCC. Conclusion: APCDD1L-AS1 was able to inhibit the progression of ccRCC, and its decreased expression could be caused by DNA hypermethylation and loss of VHL protein expression. Therefore, APCDD1L-AS1 may serve as a new therapeutic target in the treatment of ccRCC.

Keywords: APCDD1L-AS1; DNA hypermethylation; clear cell renal cell carcinoma; long non-coding RNA; von Hippel Lindau.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carcinoma, Renal Cell* / metabolism
  • Carcinoma, Squamous Cell* / genetics
  • Cell Line, Tumor
  • DNA / metabolism
  • DNA Methylation / genetics
  • Down-Regulation / genetics
  • Gene Expression Regulation, Neoplastic / genetics
  • Head and Neck Neoplasms*
  • Humans
  • Kidney Neoplasms* / metabolism
  • Mouth Neoplasms* / genetics
  • RNA, Long Noncoding* / genetics
  • RNA, Long Noncoding* / metabolism
  • Von Hippel-Lindau Tumor Suppressor Protein / genetics

Substances

  • RNA, Long Noncoding
  • DNA
  • Von Hippel-Lindau Tumor Suppressor Protein
  • VHL protein, human