Temozolomide (TZM) is a DNA-methylating agent that has recently been introduced into various clinical trials for treatment of solid or hematologic neoplasias, including brain lymphomas. In the current study, we have investigated whether the antitumor activity of TZM could be selectively enhanced at the central nervous system (CNS) site by intracerebral injection of a poly(ADP-ribose) polymerase (PARP) inhibitor. Mice were injected intracranially with lymphoma cells. The PARP inhibitor NU1025 (1 mg/animal) was delivered intracerebrally, whereas TZM was given as a single or a fractionated dose of 200 mg/kg by intraperitoneal administration, Results indicated that this drug combination significantly enhanced the survival of tumor-bearing mice and that this fractionated modality of treatment was the most effective schedule. Increased survival time was related to a marked reduction of tumor growth, as evidenced by histologic studies. Treatment With TZM alone was ineffective. This is the first report exploring in vivo the combination of TZM with PARP inhibitor for intracerebral neoplasias.

Tentori, L., Leonetti, C., Scarsella, M., D'Amati, G., Portarena, I., Zupi, G., et al. (2002). Combined treatment with temozolomide and poly(ADP-ribose) polymerase inhibitor enhances survival of mice bearing hematologic malignancy at the central nervous system site. BLOOD, 99(6), 2241-2244 [10.1182/blood.V99.6.2241].

Combined treatment with temozolomide and poly(ADP-ribose) polymerase inhibitor enhances survival of mice bearing hematologic malignancy at the central nervous system site

TENTORI, LUCIO;BONMASSAR, ENZO;GRAZIANI, GRAZIA
2002-01-01

Abstract

Temozolomide (TZM) is a DNA-methylating agent that has recently been introduced into various clinical trials for treatment of solid or hematologic neoplasias, including brain lymphomas. In the current study, we have investigated whether the antitumor activity of TZM could be selectively enhanced at the central nervous system (CNS) site by intracerebral injection of a poly(ADP-ribose) polymerase (PARP) inhibitor. Mice were injected intracranially with lymphoma cells. The PARP inhibitor NU1025 (1 mg/animal) was delivered intracerebrally, whereas TZM was given as a single or a fractionated dose of 200 mg/kg by intraperitoneal administration, Results indicated that this drug combination significantly enhanced the survival of tumor-bearing mice and that this fractionated modality of treatment was the most effective schedule. Increased survival time was related to a marked reduction of tumor growth, as evidenced by histologic studies. Treatment With TZM alone was ineffective. This is the first report exploring in vivo the combination of TZM with PARP inhibitor for intracerebral neoplasias.
2002
Pubblicato
Rilevanza internazionale
Articolo
Sì, ma tipo non specificato
Settore BIO/14 - FARMACOLOGIA
English
Con Impact Factor ISI
8 hydroxy 2 methyl 4(3h) quinazolinone; 8 hydroxy 2 methylquinazolin 4 yl; enzyme inhibitor; nicotinamide adenine dinucleotide adenosine diphosphate ribosyltransferase; temozolomide; unclassified drug; animal cell; animal experiment; animal model; antineoplastic activity; article; blood disease; brain lymphoma; cancer combination chemotherapy; central nervous system tumor; controlled study; DNA methylation; drug efficacy; fractionation; male; mouse; nonhuman; priority journal; survival time; tumor growth; Animals; Antineoplastic Combined Chemotherapy Protocols; Central Nervous System Neoplasms; Dacarbazine; Drug Evaluation, Preclinical; Hematologic Neoplasms; Male; Mice; Mice, Inbred C57BL; Mice, Inbred DBA; Poly(ADP-ribose) Polymerases; Quinazolines; Survival Analysis; Survival Rate
Tentori, L., Leonetti, C., Scarsella, M., D'Amati, G., Portarena, I., Zupi, G., et al. (2002). Combined treatment with temozolomide and poly(ADP-ribose) polymerase inhibitor enhances survival of mice bearing hematologic malignancy at the central nervous system site. BLOOD, 99(6), 2241-2244 [10.1182/blood.V99.6.2241].
Tentori, L; Leonetti, C; Scarsella, M; D'Amati, G; Portarena, I; Zupi, G; Bonmassar, E; Graziani, G
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/52890
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