Proto-oncogene activity of melanoma antigen-A11 (MAGE-A11) regulates retinoblastoma-related p107 and E2F1 proteins

J Biol Chem. 2013 Aug 23;288(34):24809-24. doi: 10.1074/jbc.M113.468579. Epub 2013 Jul 12.

Abstract

Melanoma antigen-A11 (MAGE-A11) is a low-abundance, primate-specific steroid receptor coregulator in normal tissues of the human reproductive tract that is expressed at higher levels in prostate cancer. Increased expression of MAGE-A11 enhances androgen receptor transcriptional activity and promotes prostate cancer cell growth. Further investigation into the mechanisms of MAGE-A11 function in prostate cancer demonstrated interactions with the retinoblastoma-related protein p107 and Rb tumor suppressor but no interaction with p130 of the Rb family. MAGE-A11 interaction with p107 was associated with transcriptional repression in cells with low MAGE-A11 and transcriptional activation in cells with higher MAGE-A11. Selective interaction of MAGE-A11 with retinoblastoma family members suggested the regulation of E2F transcription factors. MAGE-A11 stabilized p107 by inhibition of ubiquitination and linked p107 to hypophosphorylated E2F1 in association with the stabilization and activation of E2F1. The androgen receptor and MAGE-A11 modulated endogenous expression of the E2F1-regulated cyclin-dependent kinase inhibitor p27(Kip1). The ability of MAGE-A11 to increase E2F1 transcriptional activity was similar to the activity of adenovirus early oncoprotein E1A and depended on MAGE-A11 interactions with p107 and p300. The immunoreactivity of p107 and MAGE-A11 was greater in advanced prostate cancer than in benign prostate, and knockdown with small inhibitory RNA showed that p107 is a transcriptional activator in prostate cancer cells. These results suggest that MAGE-A11 is a proto-oncogene whose increased expression in prostate cancer reverses retinoblastoma-related protein p107 from a transcriptional repressor to a transcriptional activator of the androgen receptor and E2F1.

Keywords: Androgen Receptor; Cell Cycle Regulation; E2F Transcription Factor; Gene Transcription; MAGE-A11; Melanoma Antigen-A11; Prostate Cancer; Retinoblastoma (Rb); Steroid Receptor Coregulator; p107.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adenovirus E1A Proteins / genetics
  • Adenovirus E1A Proteins / metabolism
  • Animals
  • Antigens, Neoplasm / genetics
  • Antigens, Neoplasm / metabolism*
  • COS Cells
  • Chlorocebus aethiops
  • Cyclin-Dependent Kinase Inhibitor p27 / genetics
  • Cyclin-Dependent Kinase Inhibitor p27 / metabolism
  • E1A-Associated p300 Protein / genetics
  • E1A-Associated p300 Protein / metabolism
  • E2F1 Transcription Factor / genetics
  • E2F1 Transcription Factor / metabolism*
  • HeLa Cells
  • Humans
  • Male
  • Neoplasm Proteins / genetics
  • Neoplasm Proteins / metabolism*
  • Phosphorylation / genetics
  • Prostatic Neoplasms / genetics
  • Prostatic Neoplasms / metabolism*
  • Prostatic Neoplasms / pathology
  • Protein Stability
  • Proto-Oncogene Mas
  • Receptors, Androgen / biosynthesis
  • Receptors, Androgen / genetics
  • Retinoblastoma-Like Protein p107 / genetics
  • Retinoblastoma-Like Protein p107 / metabolism*
  • Transcription, Genetic*

Substances

  • Adenovirus E1A Proteins
  • Antigens, Neoplasm
  • CDKN1B protein, human
  • E2F1 Transcription Factor
  • E2F1 protein, human
  • MAGEA11 protein, human
  • MAS1 protein, human
  • Neoplasm Proteins
  • Proto-Oncogene Mas
  • RBL1 protein, human
  • Receptors, Androgen
  • Retinoblastoma-Like Protein p107
  • Cyclin-Dependent Kinase Inhibitor p27
  • E1A-Associated p300 Protein
  • EP300 protein, human