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Volumn 31, Issue 9, 2007, Pages 1163-1164

A new era for ribonucleoside reductase inhibition

Author keywords

Hydroxyurea resistance; Refractory leukemia; Ribonucelotide reductase inhibitors; Triapine

Indexed keywords

1 ACETYL 1,2 BIS(METHYLSULFONYL) 2 (2 CHLOROETHYL)HYDRAZINE; ANTINEOPLASTIC AGENT; CISPLATIN; DOXORUBICIN; ENZYME INHIBITOR; ETOPOSIDE; HYDROXYUREA; RIBONUCLEOSIDE REDUCTASE INHIBITOR; TRIAPTINE; UNCLASSIFIED DRUG; 3 AMINOPICOLINALDEHYDE THIOSEMICARBAZONE; 3-AMINOPYRIDINE-2-CARBOXALDEHYDE THIOSEMICARBAZONE; PYRIDINE DERIVATIVE; RIBONUCLEOTIDE REDUCTASE; THIOSEMICARBAZONE DERIVATIVE;

EID: 34249909530     PISSN: 01452126     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.leukres.2007.02.010     Document Type: Editorial
Times cited : (3)

References (17)
  • 1
    • 0036684318 scopus 로고    scopus 로고
    • Evolving role of ribonucleoside reductase inhibitors in hematologic malignancies
    • Tsimberidou A.M., Alvarado Y., and Giles F.J. Evolving role of ribonucleoside reductase inhibitors in hematologic malignancies. Expert Rev Anticancer Ther 2 (2002) 437-448
    • (2002) Expert Rev Anticancer Ther , vol.2 , pp. 437-448
    • Tsimberidou, A.M.1    Alvarado, Y.2    Giles, F.J.3
  • 2
    • 0027177564 scopus 로고
    • From RNA to DNA, why so many ribonucleotide reductases?
    • Reichard P. From RNA to DNA, why so many ribonucleotide reductases?. Science 260 (1993) 1773-1777
    • (1993) Science , vol.260 , pp. 1773-1777
    • Reichard, P.1
  • 4
    • 0024236511 scopus 로고
    • Ribonucleotide reductase as a chemotherapeutic target
    • Cory J.G. Ribonucleotide reductase as a chemotherapeutic target. Adv Enzyme Regul 27 (1988) 437-455
    • (1988) Adv Enzyme Regul , vol.27 , pp. 437-455
    • Cory, J.G.1
  • 5
    • 0022235770 scopus 로고
    • Drug action on ribonucleotide reductase
    • Cory J.G., and Carter G.L. Drug action on ribonucleotide reductase. Adv Enzyme Regul 24 (1985) 385-401
    • (1985) Adv Enzyme Regul , vol.24 , pp. 385-401
    • Cory, J.G.1    Carter, G.L.2
  • 6
    • 0035036499 scopus 로고    scopus 로고
    • Syntheses and antitumor activities of potent inhibitors of ribonucleotide reductase: 3-amino-4-methylpyridine-2-carboxaldehyde-thiosemicarba-zone (3-AMP), 3-amino-pyridine-2-carboxaldehyde-thiosemicarbazone (3-AP) and its water-soluble prodrugs
    • Li J., Zheng L.M., King I., Doyle T.W., and Chen S.H. Syntheses and antitumor activities of potent inhibitors of ribonucleotide reductase: 3-amino-4-methylpyridine-2-carboxaldehyde-thiosemicarba-zone (3-AMP), 3-amino-pyridine-2-carboxaldehyde-thiosemicarbazone (3-AP) and its water-soluble prodrugs. Curr Med Chem 8 (2001) 121-133
    • (2001) Curr Med Chem , vol.8 , pp. 121-133
    • Li, J.1    Zheng, L.M.2    King, I.3    Doyle, T.W.4    Chen, S.H.5
  • 7
    • 33646734458 scopus 로고    scopus 로고
    • In vitro and in vivo radiosensitization induced by the ribonucleotide reductase inhibitor Triapine (3-aminopyridine-2-carboxaldehyde-thiosemicarbazone)
    • Barker C.A., Burgan W.E., Carter D.J., et al. In vitro and in vivo radiosensitization induced by the ribonucleotide reductase inhibitor Triapine (3-aminopyridine-2-carboxaldehyde-thiosemicarbazone). Clin Cancer Res 12 (2006) 2912-2918
    • (2006) Clin Cancer Res , vol.12 , pp. 2912-2918
    • Barker, C.A.1    Burgan, W.E.2    Carter, D.J.3
  • 8
    • 0042563157 scopus 로고    scopus 로고
    • Phase I and pharmacodynamic study of Triapine, a novel ribonucleotide reductase inhibitor, in patients with advanced leukemia
    • Giles F.J., Fracasso P.M., Kantarjian H.M., et al. Phase I and pharmacodynamic study of Triapine, a novel ribonucleotide reductase inhibitor, in patients with advanced leukemia. Leuk Res 27 (2003) 1077-1083
    • (2003) Leuk Res , vol.27 , pp. 1077-1083
    • Giles, F.J.1    Fracasso, P.M.2    Kantarjian, H.M.3
  • 10
    • 0031923969 scopus 로고    scopus 로고
    • Pharmacokinetics and pharmacodynamics of hydroxyurea
    • Gwilt P.R., and Tracewell W.G. Pharmacokinetics and pharmacodynamics of hydroxyurea. Clin Pharmacokinet 34 (1998) 347-358
    • (1998) Clin Pharmacokinet , vol.34 , pp. 347-358
    • Gwilt, P.R.1    Tracewell, W.G.2
  • 11
    • 0023025598 scopus 로고
    • Changes of deoxyribonucleoside triphosphate pools induced by hydroxyurea and their relation to DNA synthesis
    • Bianchi V., Pontis E., and Reichard P. Changes of deoxyribonucleoside triphosphate pools induced by hydroxyurea and their relation to DNA synthesis. J Biol Chem 261 (1986) 16037-16042
    • (1986) J Biol Chem , vol.261 , pp. 16037-16042
    • Bianchi, V.1    Pontis, E.2    Reichard, P.3
  • 12
    • 0036042522 scopus 로고    scopus 로고
    • Phase I and pharmacokinetic study of 3-aminopyridine-2-carboxaldehyde thiosemicarbazone (3-AP) using a single intravenous dose schedule
    • Feun L., Modiano M., Lee K., et al. Phase I and pharmacokinetic study of 3-aminopyridine-2-carboxaldehyde thiosemicarbazone (3-AP) using a single intravenous dose schedule. Cancer Chemother Pharmacol 50 (2002) 223-229
    • (2002) Cancer Chemother Pharmacol , vol.50 , pp. 223-229
    • Feun, L.1    Modiano, M.2    Lee, K.3
  • 13
    • 4644288941 scopus 로고    scopus 로고
    • A phase I trial of 3-aminopyridine-2-carboxaldehyde thiosemicarbazone in combination with gemcitabine for patients with advanced cancer
    • Yen Y., Margolin K., Doroshow J., et al. A phase I trial of 3-aminopyridine-2-carboxaldehyde thiosemicarbazone in combination with gemcitabine for patients with advanced cancer. Cancer Chemother Pharmacol 54 (2004) 331-342
    • (2004) Cancer Chemother Pharmacol , vol.54 , pp. 331-342
    • Yen, Y.1    Margolin, K.2    Doroshow, J.3
  • 14
    • 2442698003 scopus 로고    scopus 로고
    • Phase I and pharmacokinetic study of the ribonucleotide reductase inhibitor, 3-aminopyridine-2-carboxaldehyde thiosemicarbazone, administered by 96-hour intravenous continuous infusion
    • Wadler S., Makower D., Clairmont C., Lambert P., Fehn K., and Sznol M. Phase I and pharmacokinetic study of the ribonucleotide reductase inhibitor, 3-aminopyridine-2-carboxaldehyde thiosemicarbazone, administered by 96-hour intravenous continuous infusion. J Clin Oncol 22 (2004) 1553-1563
    • (2004) J Clin Oncol , vol.22 , pp. 1553-1563
    • Wadler, S.1    Makower, D.2    Clairmont, C.3    Lambert, P.4    Fehn, K.5    Sznol, M.6
  • 15
    • 33744526999 scopus 로고    scopus 로고
    • Triapine and cytarabine is an active combination in patients with acute leukemia or myelodysplastic syndrome
    • Yee K.W., Cortes J., Ferrajoli A., et al. Triapine and cytarabine is an active combination in patients with acute leukemia or myelodysplastic syndrome. Leuk Res 30 (2006) 813-822
    • (2006) Leuk Res , vol.30 , pp. 813-822
    • Yee, K.W.1    Cortes, J.2    Ferrajoli, A.3
  • 16
    • 34249888204 scopus 로고    scopus 로고
    • Phase I and pharmacokinetic study of Triapine, a potent ribonucleotide reductase inhibitor, in adults with advanced hematologic malignancies
    • Gojo I., Tidwell M.L., Greer J., et al. Phase I and pharmacokinetic study of Triapine, a potent ribonucleotide reductase inhibitor, in adults with advanced hematologic malignancies. Leuk Res 31 (2007) 1183-1191
    • (2007) Leuk Res , vol.31 , pp. 1183-1191
    • Gojo, I.1    Tidwell, M.L.2    Greer, J.3
  • 17
    • 0033975268 scopus 로고    scopus 로고
    • Triapine (3-aminopyridine-2-carboxaldehyde- thiosemicarbazone): A potent inhibitor of ribonucleotide reductase activity with broad spectrum antitumor activity
    • Finch R.A., Liu M., Grill S.P., et al. Triapine (3-aminopyridine-2-carboxaldehyde- thiosemicarbazone): A potent inhibitor of ribonucleotide reductase activity with broad spectrum antitumor activity. Biochem Pharmacol 59 (2000) 983-991
    • (2000) Biochem Pharmacol , vol.59 , pp. 983-991
    • Finch, R.A.1    Liu, M.2    Grill, S.P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.