Integration of transcriptome and methylome analysis of aldosterone-producing adenomas

Eur J Endocrinol. 2015 Aug;173(2):185-95. doi: 10.1530/EJE-15-0148. Epub 2015 May 7.

Abstract

Objective: The pathophysiology of aldosterone-producing adenomas (APA) has been investigated intensively through genetic and genomic approaches. However, the role of epigenetics in APA is not fully understood. In the present study, we explored the relationship between gene expression and DNA methylation status in APA.

Methods: We conducted an integrated analysis of transcriptome and methylome data of paired APA-adjacent adrenal gland (AAG) samples from the same patient. The adrenal specimens were obtained from seven Japanese patients with APA who underwent adrenalectomy. Gene expression and genome-wide CpG methylation profiles were obtained from RNA and DNA samples that were extracted from those seven paired tissues.

Results: Methylome analysis showed global CpG hypomethylation in APA relative to AAG. The integration of gene expression and methylation status showed that 34 genes were up-regulated with CpG hypomethylation in APA. Of these, three genes (CYP11B2, MC2R, and HPX) may be related to aldosterone production, and five genes (PRRX1, RAB38, FAP, GCNT2, and ASB4) are potentially involved in tumorigenesis.

Conclusion: The present study is the first methylome analysis to compare APA with AAG in the same patients. Our integrated analysis of transcriptome and methylome revealed DNA hypomethylation in APA and identified several up-regulated genes with DNA hypomethylation that may be involved in aldosterone production and tumorigenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenoma / diagnosis
  • Adenoma / genetics*
  • Adenoma / surgery
  • Adrenal Gland Neoplasms / diagnosis
  • Adrenal Gland Neoplasms / genetics*
  • Adrenal Gland Neoplasms / surgery
  • Adrenalectomy / trends
  • Adult
  • Aged
  • Aldosterone / metabolism
  • DNA Methylation / genetics*
  • Female
  • Humans
  • Hyperaldosteronism / diagnosis
  • Hyperaldosteronism / genetics*
  • Hyperaldosteronism / surgery
  • Male
  • Middle Aged
  • Transcriptome / genetics*

Substances

  • Aldosterone