Combination of SAHA and bortezomib up-regulates CDKN2A and CDKN1A and induces apoptosis of Epstein-Barr virus-positive Wp-restricted Burkitt lymphoma and lymphoblastoid cell lines

Br J Haematol. 2014 Dec;167(5):639-50. doi: 10.1111/bjh.13089. Epub 2014 Aug 25.

Abstract

Epstein-Barr virus (EBV) latent proteins exert anti-apoptotic effects on EBV-transformed lymphoid cells by down-regulating BCL2L11 (BIM), CDKN2A (p16(INK4A) ) and CDKN1A (p21(WAF1) ). However, the potential therapeutic effects of targeting these anti-apoptotic mechanisms remain unexplored. Here, we tested both in vitro and in vivo effects of the combination of histone deacetylase (HDAC) and proteasome inhibitors on the apoptosis of six endemic Burkitt lymphoma (BL) lines of different latency patterns (types I and III and Wp-restricted) and three lymphoblastoid cell lines (LCLs). We found that the combination of HDAC and proteasome inhibitors (e.g. SAHA/bortezomib) synergistically induced the killing of Wp-restricted and latency III BL and LCLs but not latency I BL cells. The synergistic killing was due to apoptosis, as evidenced by the high percentage of annexin V positivity and strong cleavage of PARP1 (PARP) and CASP3 (caspase-3). Concomitantly, SAHA/bortezomib up-regulated the expression of CDKN2A and CDKN1A but did not affect the level of BCL2L11 or BHRF1 (viral homologue of BCL2). The apoptotic effects were dependent on reactive oxygen species generation. Furthermore, SAHA/bortezomib suppressed the growth of Wp-restricted BL xenografts in nude mice. This study provides the rationale to test the novel application of SAHA/bortezomib on the treatment of EBV-associated Wp-restricted BL and post-transplant lymphoproliferative disorder.

Keywords: Burkitt lymphoma; Epstein-Barr virus; histone deacetylase inhibitor; lymphoblastoid cell lines; proteasome inhibitor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Annexin A5 / metabolism
  • Antineoplastic Combined Chemotherapy Protocols / pharmacology*
  • Apoptosis / drug effects*
  • Apoptosis Regulatory Proteins / metabolism
  • Bcl-2-Like Protein 11
  • Boronic Acids / pharmacology
  • Bortezomib
  • Burkitt Lymphoma* / drug therapy
  • Burkitt Lymphoma* / metabolism
  • Burkitt Lymphoma* / pathology
  • Burkitt Lymphoma* / virology
  • Caspase 3 / metabolism
  • Cell Line, Tumor
  • Cyclin-Dependent Kinase Inhibitor p16 / biosynthesis*
  • Cyclin-Dependent Kinase Inhibitor p21 / biosynthesis*
  • Epstein-Barr Virus Infections* / drug therapy
  • Epstein-Barr Virus Infections* / metabolism
  • Epstein-Barr Virus Infections* / pathology
  • Gene Expression Regulation, Neoplastic / drug effects*
  • Herpesvirus 4, Human / metabolism*
  • Histone Deacetylase Inhibitors / pharmacology
  • Humans
  • Membrane Proteins / metabolism
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • Poly (ADP-Ribose) Polymerase-1
  • Poly(ADP-ribose) Polymerases / metabolism
  • Proteasome Inhibitors / pharmacology
  • Proto-Oncogene Proteins / metabolism
  • Pyrazines / pharmacology
  • Up-Regulation / drug effects*
  • Viral Proteins / metabolism
  • Xenograft Model Antitumor Assays / methods

Substances

  • Annexin A5
  • Apoptosis Regulatory Proteins
  • BCL2L11 protein, human
  • BHRF1 protein, Human herpesvirus 4
  • Bcl-2-Like Protein 11
  • Bcl2l11 protein, mouse
  • Boronic Acids
  • CDKN1A protein, human
  • Cyclin-Dependent Kinase Inhibitor p16
  • Cyclin-Dependent Kinase Inhibitor p21
  • Histone Deacetylase Inhibitors
  • Membrane Proteins
  • Proteasome Inhibitors
  • Proto-Oncogene Proteins
  • Pyrazines
  • Viral Proteins
  • Bortezomib
  • PARP1 protein, human
  • Poly (ADP-Ribose) Polymerase-1
  • Poly(ADP-ribose) Polymerases
  • CASP3 protein, human
  • Caspase 3