Premium
Suberoylanilide hydroxamic acid (SAHA) combined with bortezomib inhibits renal cancer growth by enhancing histone acetylation and protein ubiquitination synergistically
Author(s) -
Sato Akinori,
Asano Takako,
Ito Keiichi,
Sumitomo Makoto,
Asano Tomohiko
Publication year - 2012
Publication title -
bju international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.773
H-Index - 148
eISSN - 1464-410X
pISSN - 1464-4096
DOI - 10.1111/j.1464-410x.2011.10533.x
Subject(s) - bortezomib , acetylation , histone deacetylase , vorinostat , cancer research , cancer cell , apoptosis , histone deacetylase inhibitor , proteasome inhibitor , cancer , chemistry , pharmacology , cell growth , histone , proteasome , in vivo , cell cycle , biology , multiple myeloma , medicine , biochemistry , immunology , microbiology and biotechnology , gene
What's known on the subject? and What does the study add? The treatment modality for advanced renal cancer is limited and new treatment approaches are urgently needed. Beneficial effects of bortezomib combined with SAHA have recently been reported. However, there are no previous reports of this combination being tested against renal cancer and its further mechanisms of action should be clarified. This study examined the combined effects of these two clinically feasible drugs and showed that the combination inhibits renal cancer cell proliferation by enhancing both protein ubiquitination and histone acetylation synergistically. OBJECTIVE• To investigate the combined effect of two clinically feasible drugs, the proteasome inhibitor bortezomib and the histone deacetylase (HDAC) inhibitor suberoylanilide hydroxamic acid (SAHA), on human renal cancer cells in vitro and in vivo .MATERIALS AND METHODS• The effectiveness of the combination of bortezomib (10–20 n m ) and SAHA (1–5 µ m ) on renal cancer cells (Caki‐1, ACHN, A‐498, 786‐O, 769‐P) was assessed by MTS assay, colony formation assay, cell cycle analysis, and apoptosis assay. • In vivo efficacy was evaluated using murine subcutaneous (s.c.) tumour models. • Protein ubiquitination, unfolded protein response, histone acetylation, and changes in the expression of HDAC were evaluated by western blotting.RESULTS• The combination of SAHA and bortezomib induced apoptosis and inhibited cancer cell proliferation synergistically (combination indices <1) and colony formation significantly ( P < 0.05). • In s.c. tumour models a 10‐day treatment with a combination of SAHA (50 mg/kg) and bortezomib (60 µg/kg) inhibited tumour growth significantly ( P < 0.05). • Mechanistically, SAHA combined with bortezomib enhanced protein ubiquitination synergistically and enhanced histone acetylation by inhibiting the expression of HDACs.CONCLUSION• SAHA combined with bortezomib inhibits the proliferation of renal cancer cells in vitro and in vivo , and the effectiveness of the combination is due to its synergistic enhancement of histone acetylation and protein ubiquitination.