Interferon γ is a strong, STAT1-dependent direct inducer of BCL6 expression in multiple myeloma cells

Biochem Biophys Res Commun. 2018 Apr 6;498(3):502-508. doi: 10.1016/j.bbrc.2018.03.010. Epub 2018 Mar 3.

Abstract

B-cell CLL/lymphoma 6 (BCL6) is a transcriptional master regulator that can repress more than 1200 potential target genes. It exerts oncogenic effects through the inhibition of differentiation, DNA damage sensing and apoptosis in several human hematopoietic malignancies, including multiple myeloma (MM). The multifunctional cytokine interferon γ (IFNγ) exerts pro-apoptotic and anti-proliferative effects on MM cells in vitro, at least partially through the inhibition of the effects of interleukin 6 (IL6), one of the most important growth factor of MM and a strong inducer of BCL6 expression. However, IFNγ was also reported to directly upregulate BCL6 in several cell types. These observations prompted us to analyze the effect of IFNγ on BCL6 expression in MM cells. We discovered that among several myeloma growth/survival factors tested (including IL6, oncostatin M, insulin-like growth factor 1, tumor necrosis factor α and IFNα) IFNγ was the strongest inducer of BCL6 mRNA and protein expression in MM cell lines. IFNγ induced upregulation of BCL6 was dependent on the classical STAT1 signaling pathway, and affected both major BCL6 variants. Interestingly, although IFNα induced stronger STAT1 phosphorylation than IFNγ, it only slightly upregulated BCL6 in MM lines. We proved that IFNα induced BCL6 upregulation was limited by the concomitant activation of STAT5 signaling. We assume that BCL6 upregulation may represent a potentially pro-tumorigenic effect of IFNγ signaling in MM cells.

Keywords: BCL6; IFNγ; Multiple myeloma; STAT1; STAT5.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line, Tumor
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • Interferon-gamma / metabolism*
  • Multiple Myeloma / genetics*
  • Multiple Myeloma / metabolism
  • Proto-Oncogene Proteins c-bcl-6 / genetics*
  • STAT1 Transcription Factor / metabolism*
  • STAT5 Transcription Factor / metabolism
  • Signal Transduction
  • Tumor Suppressor Proteins / metabolism
  • Up-Regulation*

Substances

  • BCL6 protein, human
  • Proto-Oncogene Proteins c-bcl-6
  • STAT1 Transcription Factor
  • STAT1 protein, human
  • STAT5 Transcription Factor
  • STAT5A protein, human
  • Tumor Suppressor Proteins
  • Interferon-gamma