Combination therapy of established cancer using a histone deacetylase inhibitor and a TRAIL receptor agonist

被引:119
作者
Frew, Ailsa J. [1 ,2 ]
Lindemann, Ralph K. [3 ]
Martin, Ben P. [1 ]
Clarke, Christopher J. P. [1 ]
Sharkey, Janelle [1 ]
Anthony, Desiree A. [1 ]
Banks, Kellie-Marie [1 ]
Haynes, Nicole M. [1 ]
Gangatirkar, Pradnya [1 ]
Stanley, Kym [1 ]
Bolden, Jessica E. [1 ]
Takeda, Kazuyoshi [4 ]
Yagita, Hideo [4 ]
Secrist, J. Paul [5 ]
Smyth, Mark J. [1 ,2 ]
Johnstone, Ricky W. [1 ,2 ]
机构
[1] Peter MacCallum Canc Inst, Canc Immunol Program, Trescowthick Res Labs, Melbourne, Vic 3002, Australia
[2] Univ Melbourne, Parkville, Vic 3010, Australia
[3] Deutsch Krebsforschungszentrum, Abt Translat Onkol, Natl Ctr Tumorerkrankungen, D-69120 Heidelberg, Germany
[4] Juntendo Univ, Sch Med, Dept Immunol, Bunkyo Ku, Tokyo 1138421, Japan
[5] Archemix Corp, Cambridge, MA 02142 USA
基金
英国医学研究理事会;
关键词
D O I
10.1073/pnas.0801868105
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学];
摘要
Histone deacetylase inhibitors (HDACi) and agents such as recombinant tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) and agonistic anti-TRAIL receptor (TRAIL-R) antibodies are anticancer agents that have shown promise in preclinical settings and in early phase clinical trials as monotherapies. Although HDACi and activators of the TRAIL pathway have different molecular targets and mechanisms of action, they share the ability to induce tumor cell-selective apoptosis. The ability of HDACi to induce expression of TRAIL-R death receptors 4 and 5 (DR4/DR5), and induce tumor cell death via the intrinsic apoptotic pathway provides a molecular rationale to combine these agents with activators of the TRAIL pathway that activate the alternative (death receptor) apoptotic pathway. Herein, we demonstrate that the HDACi vorinostat synergizes with the mouse DR5-specific monoclonal antibody MD5-1 to induce rapid and robust tumor cell apoptosis in vitro and in vivo. Importantly, using a preclinical mouse breast cancer model, we show that the combination of vorinostat and MD5-1 is safe and induces regression of established tumors, whereas single agent treatment had little or no effect. Functional analyses revealed that rather than mediating enhanced tumor cell apoptosis via the simultaneous activation of the intrinsic and extrinsic apoptotic pathways, vorinostat augmented MD5-1-induced apoptosis concomitant with down-regulation of the intracellular apoptosis inhibitor cellular-FLIP (c-FLIP). These data demonstrate that combination therapies involving HDACi and activators of the TRAIL pathway can be efficacious for the treatment of cancer in experimental mouse models.
引用
收藏
页码:11317 / 11322
页数:6
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