Signal transducer and activator of transcription 3 (STAT3) promoter methylation and expression in pituitary adenoma

BMC Med Genet. 2017 Jul 14;18(1):72. doi: 10.1186/s12881-017-0434-3.

Abstract

Background: Pituitary adenoma (PA) is a benign brain tumor that can cause neurological, endocrinological and ophthalmological aberrations. Till now there is a need to identify factors that can influence the tumor invasiveness and recurrence. The aim of this study was to evaluate the associations between the signal transducer and activator of transcription 3 (STAT3) promoter methylation, mRNA expression and the invasiveness or recurrence of PAs and patient clinical characteristics.

Methods: Study participants comprised of 102 subjects with a diagnosis of PA: 54 functioning and 48 non-functioning, 58 invasive and 30 non-invasive PAs and 14 relapses. The bisulfite treatment of tumor DNA and methylation-specific polymerase chain reaction (MS-PCR) method was used to determine the STAT3 gene promoter methylation. For the STAT3 mRNA expression, the first-strand cDNA was produced from total RNA by using reverse transcriptase and quantitative real-time PCR (qRT-PCR) was performed.

Results: In 10.78% (11/102) of PA tissues STAT3 gene promoter was methylated. A gender of male and patient group older than 60 years were significantly associated with reduced STAT3 mRNA expression (Mann-Whitney test, p = 0.025, p = 0.047, respectively). However, no more statistical differences were found between STAT3 promoter methylation, mRNA expression and patient clinical characteristics or PA invasiveness or recurrence.

Conclusions: Further investigations are needed to clarify the influence of STAT3 gene promoter methylation and mRNA expression changes in PAs.

Keywords: DNA methylation; Invasiveness; Pituitary adenoma; Signal transducer and activator of transcription 3; mRNA expression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • DNA Methylation
  • Female
  • Humans
  • Male
  • Middle Aged
  • Neoplasm Invasiveness / genetics
  • Neoplasm Recurrence, Local / genetics
  • Pituitary Neoplasms / genetics*
  • Promoter Regions, Genetic*
  • RNA, Messenger / metabolism
  • RNA, Neoplasm / metabolism
  • Real-Time Polymerase Chain Reaction
  • STAT3 Transcription Factor / genetics*

Substances

  • RNA, Messenger
  • RNA, Neoplasm
  • STAT3 Transcription Factor