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Dual targeting of histone deacetylase and topoisomerase II with novel bifunctional inhibitors.


ABSTRACT: Strategies to ameliorate the flaws of current chemotherapeutic agents, while maintaining potent anticancer activity, are of particular interest. Agents which can modulate multiple targets may have superior utility and fewer side effects than current single-target drugs. To explore the prospect in cancer therapy of a bivalent agent that combines two complementary chemo-active groups within a single molecular architecture, we have synthesized dual-acting histone deacetylase and topoisomerase II inhibitors. These dual-acting agents are derived from suberoylanilide hydroxamic acid (SAHA) and anthracycline daunorubicin, prototypical histone deacetylase (HDAC) and topoisomerase II (Topo II) inhibitors, respectively. We report herein that these agents present the signatures of inhibition of HDAC and Topo II in both cell-free and whole-cell assays. Moreover, these agents potently inhibit the proliferation of representative cancer cell lines.

SUBMITTER: Guerrant W 

PROVIDER: S-EPMC3306125 | biostudies-literature | 2012 Feb

REPOSITORIES: biostudies-literature

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Dual targeting of histone deacetylase and topoisomerase II with novel bifunctional inhibitors.

Guerrant William W   Patil Vishal V   Canzoneri Joshua C JC   Oyelere Adegboyega K AK  

Journal of medicinal chemistry 20120213 4


Strategies to ameliorate the flaws of current chemotherapeutic agents, while maintaining potent anticancer activity, are of particular interest. Agents which can modulate multiple targets may have superior utility and fewer side effects than current single-target drugs. To explore the prospect in cancer therapy of a bivalent agent that combines two complementary chemo-active groups within a single molecular architecture, we have synthesized dual-acting histone deacetylase and topoisomerase II in  ...[more]

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