Regulation of OCT2 transcriptional repression by histone acetylation in renal cell carcinoma

Epigenetics. 2019 Aug;14(8):791-803. doi: 10.1080/15592294.2019.1615354. Epub 2019 May 15.

Abstract

Renal cell carcinoma (RCC) is a common malignant tumour affecting the urinary system, and multidrug resistance is one of the major reasons why chemotherapy for this type of cancer often fails. Previous studies have shown that loss of the human organic cation transporter OCT2 is the main factor contributing to oxaliplatin resistance in RCC, and that DNA hypermethylation and histone methylation play important roles in the transcriptional repression of OCT2 in RCC. In this study, we found that histone acetylation also regulates OCT2 repression in RCC and elucidated the underlying mechanisms. In normal renal cells, HDAC7 combines with MYC at the OCT2 promoter, resulting in a decrease in free HDAC7, which in turn increases the levels of H3K18ac and H3K27ac at the OCT2 promotor and activates OCT2 expression. In RCC cells, however, the interaction between HDAC7 and MYC does not occur, which leads a high abundance of HDAC7 and low levels of H3K18ac and H3K27ac at the OCT2 promoter, thereby resulting in the inhibition of OCT2 transcription. We found that combined treatment using the DNA methylation inhibitor decitabine and the histone deacetylase inhibitor vorinostat significantly increased the expression of OCT2 in RCC cell lines, which sensitized these cells to oxaliplatin. We accordingly propose that the combination of anticancer agents and epigenetic drugs can provide a novel chemotherapeutic regimen.

Keywords: OCT2; Renal cell carcinoma; combination therapy; epigenetic regulation; histone acetylaion.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylation
  • Carcinoma, Renal Cell / genetics*
  • Carcinoma, Renal Cell / metabolism
  • Cell Line, Tumor
  • Decitabine / pharmacology
  • Down-Regulation
  • Drug Resistance, Neoplasm*
  • Epigenesis, Genetic
  • Gene Expression Regulation, Neoplastic
  • Histone Deacetylases / metabolism
  • Histones / metabolism*
  • Humans
  • Kidney Neoplasms / genetics*
  • Kidney Neoplasms / metabolism
  • Organic Cation Transporter 2 / genetics*
  • Oxaliplatin / pharmacology
  • Promoter Regions, Genetic
  • Proto-Oncogene Proteins c-myc / metabolism
  • Vorinostat / pharmacology

Substances

  • Histones
  • MYC protein, human
  • Organic Cation Transporter 2
  • Proto-Oncogene Proteins c-myc
  • SLC22A2 protein, human
  • Oxaliplatin
  • Vorinostat
  • Decitabine
  • HDAC7 protein, human
  • Histone Deacetylases

Grants and funding

This project was supported by National Natural Science Foundation of China [81773817], National Key R&D Program of China [No. 2017YFC0908600, 2017YFE0102200], and the National Natural Science Foundation of China [No. 81702801].