Abstract
We describe the synthesis and in vitro activity of drug-dye conjugate 1, which is a combination of the PARP inhibitor rucaparib and heptamethine cyanine dye IR-786. The drug-dye conjugate 1 was evaluated in three different patient-derived glioblastoma cell lines and showed strong cytotoxic activity with nanomolar potency (EC50: 128 nM), which was a 780 fold improvement over rucaparib itself. We also observe a synergistic effect of 1 with temozolomide (TMZ), the standard drug for treatment for glioblastoma even though these cell lines were resistant to TMZ treatment. We envisage such conjugates to be worth exploring for their utility in the treatment of various brain cancers.
Keywords:
Glioblastoma; Heptamethine cyanine dyes; PARP inhibitors; Rucaparib; Temozolomide.
Copyright © 2020 Elsevier Ltd. All rights reserved.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Antineoplastic Agents / chemical synthesis
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Antineoplastic Agents / chemistry
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Antineoplastic Agents / pharmacology*
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Brain Neoplasms / drug therapy*
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Brain Neoplasms / metabolism
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Brain Neoplasms / pathology
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Carbocyanines / chemistry
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Carbocyanines / pharmacology*
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Cell Line, Tumor
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Cell Proliferation / drug effects
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Cell Survival / drug effects
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Dose-Response Relationship, Drug
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Drug Screening Assays, Antitumor
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Glioblastoma / drug therapy*
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Glioblastoma / metabolism
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Glioblastoma / pathology
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Humans
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Indoles / chemistry
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Indoles / pharmacology*
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Molecular Structure
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Poly(ADP-ribose) Polymerase Inhibitors / chemical synthesis
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Poly(ADP-ribose) Polymerase Inhibitors / chemistry
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Poly(ADP-ribose) Polymerase Inhibitors / pharmacology*
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Poly(ADP-ribose) Polymerases / metabolism*
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Structure-Activity Relationship
Substances
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Antineoplastic Agents
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Carbocyanines
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IR-786
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Indoles
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Poly(ADP-ribose) Polymerase Inhibitors
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rucaparib
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Poly(ADP-ribose) Polymerases