Combined treatment with temozolomide and poly(ADP-ribose) polymerase inhibitor enhances survival of mice bearing hematologic malignancy at the central nervous system site
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作者:
Tentori, L
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机构:Univ Roma Tor Vergata, Dept Neurosci, I-00133 Rome, Italy
Tentori, L
Leonetti, C
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机构:Univ Roma Tor Vergata, Dept Neurosci, I-00133 Rome, Italy
Leonetti, C
Scarsella, M
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机构:Univ Roma Tor Vergata, Dept Neurosci, I-00133 Rome, Italy
Scarsella, M
d'Amati, G
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机构:Univ Roma Tor Vergata, Dept Neurosci, I-00133 Rome, Italy
d'Amati, G
Portarena, I
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机构:Univ Roma Tor Vergata, Dept Neurosci, I-00133 Rome, Italy
Portarena, I
Zupi, G
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机构:Univ Roma Tor Vergata, Dept Neurosci, I-00133 Rome, Italy
Zupi, G
Bonmassar, E
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机构:Univ Roma Tor Vergata, Dept Neurosci, I-00133 Rome, Italy
Bonmassar, E
Graziani, G
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机构:Univ Roma Tor Vergata, Dept Neurosci, I-00133 Rome, Italy
Graziani, G
机构:
[1] Univ Roma Tor Vergata, Dept Neurosci, I-00133 Rome, Italy
[2] Ist Dermopat Immacolata, Rome, Italy
[3] Regina Elena Canc Inst, Expt Chemotherapy Lab, Rome, Italy
[4] Univ Rome La Sapienza, Dept Expt Med & Pathol, Rome, Italy
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.
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UNIV NEWCASTLE UPON TYNE, CANC RES UNIT, NEWCASTLE UPON TYNE NE1 7RU, TYNE & WEAR, ENGLANDUNIV NEWCASTLE UPON TYNE, CANC RES UNIT, NEWCASTLE UPON TYNE NE1 7RU, TYNE & WEAR, ENGLAND
GRIFFIN, RJ
CURTIN, NJ
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UNIV NEWCASTLE UPON TYNE, CANC RES UNIT, NEWCASTLE UPON TYNE NE1 7RU, TYNE & WEAR, ENGLANDUNIV NEWCASTLE UPON TYNE, CANC RES UNIT, NEWCASTLE UPON TYNE NE1 7RU, TYNE & WEAR, ENGLAND
CURTIN, NJ
NEWELL, DR
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UNIV NEWCASTLE UPON TYNE, CANC RES UNIT, NEWCASTLE UPON TYNE NE1 7RU, TYNE & WEAR, ENGLANDUNIV NEWCASTLE UPON TYNE, CANC RES UNIT, NEWCASTLE UPON TYNE NE1 7RU, TYNE & WEAR, ENGLAND
NEWELL, DR
GOLDING, BT
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UNIV NEWCASTLE UPON TYNE, CANC RES UNIT, NEWCASTLE UPON TYNE NE1 7RU, TYNE & WEAR, ENGLANDUNIV NEWCASTLE UPON TYNE, CANC RES UNIT, NEWCASTLE UPON TYNE NE1 7RU, TYNE & WEAR, ENGLAND
GOLDING, BT
DURKACZ, BW
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UNIV NEWCASTLE UPON TYNE, CANC RES UNIT, NEWCASTLE UPON TYNE NE1 7RU, TYNE & WEAR, ENGLANDUNIV NEWCASTLE UPON TYNE, CANC RES UNIT, NEWCASTLE UPON TYNE NE1 7RU, TYNE & WEAR, ENGLAND
DURKACZ, BW
CALVERT, AH
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UNIV NEWCASTLE UPON TYNE, CANC RES UNIT, NEWCASTLE UPON TYNE NE1 7RU, TYNE & WEAR, ENGLANDUNIV NEWCASTLE UPON TYNE, CANC RES UNIT, NEWCASTLE UPON TYNE NE1 7RU, TYNE & WEAR, ENGLAND
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UNIV NEWCASTLE UPON TYNE, CANC RES UNIT, NEWCASTLE UPON TYNE NE1 7RU, TYNE & WEAR, ENGLANDUNIV NEWCASTLE UPON TYNE, CANC RES UNIT, NEWCASTLE UPON TYNE NE1 7RU, TYNE & WEAR, ENGLAND
GRIFFIN, RJ
CURTIN, NJ
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UNIV NEWCASTLE UPON TYNE, CANC RES UNIT, NEWCASTLE UPON TYNE NE1 7RU, TYNE & WEAR, ENGLANDUNIV NEWCASTLE UPON TYNE, CANC RES UNIT, NEWCASTLE UPON TYNE NE1 7RU, TYNE & WEAR, ENGLAND
CURTIN, NJ
NEWELL, DR
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UNIV NEWCASTLE UPON TYNE, CANC RES UNIT, NEWCASTLE UPON TYNE NE1 7RU, TYNE & WEAR, ENGLANDUNIV NEWCASTLE UPON TYNE, CANC RES UNIT, NEWCASTLE UPON TYNE NE1 7RU, TYNE & WEAR, ENGLAND
NEWELL, DR
GOLDING, BT
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UNIV NEWCASTLE UPON TYNE, CANC RES UNIT, NEWCASTLE UPON TYNE NE1 7RU, TYNE & WEAR, ENGLANDUNIV NEWCASTLE UPON TYNE, CANC RES UNIT, NEWCASTLE UPON TYNE NE1 7RU, TYNE & WEAR, ENGLAND
GOLDING, BT
DURKACZ, BW
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UNIV NEWCASTLE UPON TYNE, CANC RES UNIT, NEWCASTLE UPON TYNE NE1 7RU, TYNE & WEAR, ENGLANDUNIV NEWCASTLE UPON TYNE, CANC RES UNIT, NEWCASTLE UPON TYNE NE1 7RU, TYNE & WEAR, ENGLAND
DURKACZ, BW
CALVERT, AH
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UNIV NEWCASTLE UPON TYNE, CANC RES UNIT, NEWCASTLE UPON TYNE NE1 7RU, TYNE & WEAR, ENGLANDUNIV NEWCASTLE UPON TYNE, CANC RES UNIT, NEWCASTLE UPON TYNE NE1 7RU, TYNE & WEAR, ENGLAND