-
1
-
-
0023552964
-
Antitumor activity of 7-ethyl-10[4-(1-piperidino)-1-piperidino] carbonyloxy-camptothecin, a novel watersoluble derivative of camptothecin, against murine tumors
-
Kunimoto T, Nitta K, Tanaka T, Uehara N, Baba H, Takeuchi M, Yokokura T, Sawada S, Miyasaka T, Mutai M: Antitumor activity of 7-ethyl-10[4-(1-piperidino) -1-piperidino] carbonyloxy-camptothecin, a novel watersoluble derivative of camptothecin, against murine tumors. Cancer Res 1987; 47: 5944-5947
-
(1987)
Cancer Res
, vol.47
, pp. 5944-5947
-
-
Kunimoto, T.1
Nitta, K.2
Tanaka, T.3
Uehara, N.4
Baba, H.5
Takeuchi, M.6
Yokokura, T.7
Sawada, S.8
Miyasaka, T.9
Mutai, M.10
-
2
-
-
0025899645
-
Synthesis and antitumor activity of 20(S)- camptothecin derivatives: Carbamate-linked, water-soluble derivatives of 7-ethyl-10-hydroxycamptothecin
-
Sawada S, Okajima S, Aiyama R, Nakata K, Furuta T, Sugino E, Yamaguchi K, Miyasaka T: Synthesis and antitumor activity of 20(S)- camptothecin derivatives: Carbamate-linked, water-soluble derivatives of 7-ethyl-10- hydroxycamptothecin. Chem Pharma Bull 1991; 39: 1446-1450
-
(1991)
Chem Pharma Bull
, vol.39
, pp. 1446-1450
-
-
Sawada, S.1
Okajima, S.2
Aiyama, R.3
Nakata, K.4
Furuta, T.5
Sugino, E.6
Yamaguchi, K.7
Miyasaka, T.8
-
4
-
-
0033800708
-
Clinical use of topoisomerase I inhibitors in anticancer treatment
-
Rodriguez-Galindo C, Radomski K, Stewart CF, Furman W, Santana VM, Houghton PJ: Clinical use of topoisomerase I inhibitors in anticancer treatment. Med Pediatr Oncol 2000; 35: 385-402
-
(2000)
Med Pediatr Oncol
, vol.35
, pp. 385-402
-
-
Rodriguez-Galindo, C.1
Radomski, K.2
Stewart, C.F.3
Furman, W.4
Santana, V.M.5
Houghton, P.J.6
-
5
-
-
0025272187
-
Metabolism and pharmacokinetics of the camptothecin analogue CPT-11 in the mouse
-
Kaneda N, Nagata H, Yokokura T: Metabolism and pharmacokinetics of the camptothecin analogue CPT-11 in the mouse. Cancer Res 1990; 50: 1715-1720
-
(1990)
Cancer Res
, vol.50
, pp. 1715-1720
-
-
Kaneda, N.1
Nagata, H.2
Yokokura, T.3
-
6
-
-
0025996996
-
Intracellular roles of SN-38, a metabolite of the camptothecin derivative CPT-11, in the antitumor effect of CPT-11
-
Kawato Y, Aonuma M, Hirota Y, Kuga H, Sato K: Intracellular roles of SN-38, a metabolite of the camptothecin derivative CPT-11, in the antitumor effect of CPT-11. Cancer Res 1991; 51: 4187-4191
-
(1991)
Cancer Res
, vol.51
, pp. 4187-4191
-
-
Kawato, Y.1
Aonuma, M.2
Hirota, Y.3
Kuga, H.4
Sato, K.5
-
7
-
-
0024324205
-
On the mechanism of topoisomerase I inhibition by camptothecin: Evidence for binding to an enzyme- DNA complex
-
Hertzberg RP, Caranfa MJ, Hecht SM: On the mechanism of topoisomerase I inhibition by camptothecin: Evidence for binding to an enzyme- DNA complex. Biochemistry 1989; 28: 4629-4638
-
(1989)
Biochemistry
, vol.28
, pp. 4629-4638
-
-
Hertzberg, R.P.1
Caranfa, M.J.2
Hecht, S.M.3
-
8
-
-
0032489634
-
Crystal structure of human topoisomerase I in covalent and noncovalent complexes with DNA
-
Redinbo MR, Stewart L, Kuhn P, Champoux JJ, Hol WG: Crystal structure of human topoisomerase I in covalent and noncovalent complexes with DNA. Science 1998; 279: 1504-1513
-
(1998)
Science
, vol.279
, pp. 1504-1513
-
-
Redinbo, M.R.1
Stewart, L.2
Kuhn, P.3
Champoux, J.J.4
Hol, W.G.5
-
9
-
-
0032489675
-
A model for the mechanism of human topoisomerase I
-
Stewart L, Redinbo MR, Qiu X, Hol WG, Champoux JJ: A model for the mechanism of human topoisomerase I. Science 1998; 279: 1534-1541
-
(1998)
Science
, vol.279
, pp. 1534-1541
-
-
Stewart, L.1
Redinbo, M.R.2
Qiu, X.3
Hol, W.G.4
Champoux, J.J.5
-
10
-
-
0034509633
-
Mechanism of action of camptothecin
-
Liu LF, Desai SD, Li TK, Mao Y, Sun M, Sim SP: Mechanism of action of camptothecin. Ann NY Acad Sci 2000; 922: 1-10
-
(2000)
Ann NY Acad Sci
, vol.922
, pp. 1-10
-
-
Liu, L.F.1
Desai, S.D.2
Li, T.K.3
Mao, Y.4
Sun, M.5
Sim, S.P.6
-
11
-
-
0015692519
-
Effects of camptothecin on the breakage and repair of DNA during the cell cycle
-
Horwitz SB, Horwitz MS: Effects of camptothecin on the breakage and repair of DNA during the cell cycle. Cancer Res 1973; 33: 2834-2846
-
(1973)
Cancer Res
, vol.33
, pp. 2834-2846
-
-
Horwitz, S.B.1
Horwitz, M.S.2
-
12
-
-
0024420685
-
Arrest of replication forks by drug-stabilized topoisomerase I-DNA cleavable complexes as a mechanism of cell killing by camptothecin
-
Hsiang YH, Lihou MG, Liu LF: Arrest of replication forks by drug-stabilized topoisomerase I-DNA cleavable complexes as a mechanism of cell killing by camptothecin. Cancer Res 1989; 49: 5077-5082
-
(1989)
Cancer Res
, vol.49
, pp. 5077-5082
-
-
Hsiang, Y.H.1
Lihou, M.G.2
Liu, L.F.3
-
13
-
-
0027096415
-
A kinetic and mechanistic study of the hydrolysis of camptothecin and some analogues
-
Fassberg J, Stella VJ: A kinetic and mechanistic study of the hydrolysis of camptothecin and some analogues. J Pharm Sci 1992; 81: 676-684
-
(1992)
J Pharm Sci
, vol.81
, pp. 676-684
-
-
Fassberg, J.1
Stella, V.J.2
-
14
-
-
0027930186
-
Differential interactions of camptothecin lactone and carboxylate forms with human blood components
-
Mi Z, Burke TG: Differential interactions of camptothecin lactone and carboxylate forms with human blood components. Biochemistry 1994; 33: 10325-10336
-
(1994)
Biochemistry
, vol.33
, pp. 10325-10336
-
-
Mi, Z.1
Burke, T.G.2
-
15
-
-
0030716924
-
Severe CPT-11 toxicity in patients with Gilbert's syndrome: Two case reports
-
Wasserman E, Myara A, Lokiec F, Goldwasser F, Trivin F, Mahjoubi M, et al: Severe CPT-11 toxicity in patients with Gilbert's syndrome: Two case reports. Ann Oncol 1997; 8: 1049-1051
-
(1997)
Ann Oncol
, vol.8
, pp. 1049-1051
-
-
Wasserman, E.1
Myara, A.2
Lokiec, F.3
Goldwasser, F.4
Trivin, F.5
Mahjoubi, M.6
-
16
-
-
84891622616
-
Therapeutic targeting of CPT-11 induced diarrhea: A case of prophylaxis
-
Swami U, Goel S, Mani S: Therapeutic targeting of CPT-11 induced diarrhea: A case of prophylaxis. Curr Drug Targets 2013; 14: 777-779
-
(2013)
Curr Drug Targets
, Issue.14
, pp. 777-779
-
-
Swami, U.1
Goel, S.2
Mani, S.3
-
17
-
-
77649216536
-
Membrane transporters in drug development: Report from the fda critical path initiative- sponsored workshop
-
Giacomini KM, Huang SM, Tweedie DJ, Benet LZ, Brouwer KL, Chu X, et al: Membrane Transporters in Drug Development: Report from the FDA Critical Path Initiative- Sponsored Workshop. Nat Rev Drug Dis 2010; 9: 215-236
-
(2010)
Nat Rev Drug Dis
, Issue.9
, pp. 215-236
-
-
Giacomini, K.M.1
Huang, S.M.2
Tweedie, D.J.3
Benet, L.Z.4
Brouwer, K.L.5
Chu, X.6
-
18
-
-
0031717972
-
Multiplicity of biliary excretion mechanisms for the camptothecin derivative irinotecan (CPT-11), its metabolite SN-38, and its glucuronide: Role of canalicular multispecific organic anion transporter and P-glycoprotein
-
Sugiyama Y, Kato Y, Chu X: Multiplicity of biliary excretion mechanisms for the camptothecin derivative irinotecan (CPT-11), its metabolite SN-38, and its glucuronide: Role of canalicular multispecific organic anion transporter and P-glycoprotein. Cancer Chemother Pharmacol 1998; 42:S44-S49
-
(1998)
Cancer Chemother Pharmacol
, vol.42
-
-
Sugiyama, Y.1
Kato, Y.2
Chu, X.3
-
19
-
-
0035834595
-
Transport of 7-ethyl-10-hydroxycamptothecin (SN-38) by breast cancer resistance protein ABCG2 in human lung cancer cells
-
Nakatomi K, Yoshikawa M, Oka M, Ikegami Y, Hayasaka S, Sano K, et al: Transport of 7-ethyl-10-hydroxycamptothecin (SN-38) by breast cancer resistance protein ABCG2 in human lung cancer cells. Biochem Biophys Res Commun 2001; 288: 827-832
-
(2001)
Biochem Biophys Res Commun
, vol.288
, pp. 827-832
-
-
Nakatomi, K.1
Yoshikawa, M.2
Oka, M.3
Ikegami, Y.4
Hayasaka, S.5
Sano, K.6
-
20
-
-
2442638937
-
Highaffinity interaction of tyrosine kinase inhibitors with the ABCG2 multidrug transporter
-
Ozvegy-Laczka C, Hegedus T, Varady G, Ujhelly O, Schuetz JD, Varadi A, et al: Highaffinity interaction of tyrosine kinase inhibitors with the ABCG2 multidrug transporter. Mol Pharmacol 2004; 65: 1485-1495
-
(2004)
Mol Pharmacol
, vol.65
, pp. 1485-1495
-
-
Ozvegy-Laczka, C.1
Hegedus, T.2
Varady, G.3
Ujhelly, O.4
Schuetz, J.D.5
Varadi, A.6
-
21
-
-
23744502215
-
Gefitinib, an EGFR tyrosine kinase inhibitor, directly inhibits the function of P-glycoprotein in multidrug resistant cancer cells
-
Kitazaki T, Oka M, Nakamura Y, Tsurutani J, Doi S, Yasunaga M, et al: Gefitinib, an EGFR tyrosine kinase inhibitor, directly inhibits the function of P-glycoprotein in multidrug resistant cancer cells. Lung Cancer 2005; 49: 337-343
-
(2005)
Lung Cancer
, vol.49
, pp. 337-343
-
-
Kitazaki, T.1
Oka, M.2
Nakamura, Y.3
Tsurutani, J.4
Doi, S.5
Yasunaga, M.6
-
22
-
-
33646778840
-
A new strategy of high-speed screening and quantitative structure-activity relationship analysis to evaluate human ATP-binding cassette transporter ABCG2-drug interactions
-
Saito H, Hirano H, Nakagawa H, Fukami T, Oosumi K, Murakami K, et al: A new strategy of high-speed screening and quantitative structure-activity relationship analysis to evaluate human ATP-binding cassette transporter ABCG2-drug interactions. J Pharmacol Exp Ther 2006; 317: 1114-1124
-
(2006)
J Pharmacol Exp Ther
, vol.317
, pp. 1114-1124
-
-
Saito, H.1
Hirano, H.2
Nakagawa, H.3
Fukami, T.4
Oosumi, K.5
Murakami, K.6
-
23
-
-
84861139188
-
Quantitative structure- activity relationship (QSAR) analysis to predict drug-drug interactions of ABC transporter ABCG2
-
Ishikawa T, Hirano H, Saito H, Sano K, Ikegami Y, Yamaotsu N, et al: Quantitative structure- activity relationship (QSAR) analysis to predict drug-drug interactions of ABC transporter ABCG2. Mini Rev Med Chem 2012; 12: 505-514
-
(2012)
Mini Rev Med Chem
, Issue.12
, pp. 505-514
-
-
Ishikawa, T.1
Hirano, H.2
Saito, H.3
Sano, K.4
Ikegami, Y.5
Yamaotsu, N.6
-
24
-
-
13944269488
-
Gefitinib ('Iressa', ZD1839), an epidermal growth factor receptor tyrosine kinase inhibitor, reverses breast cancer resistance protein/ABCG2-mediated drug resistance
-
Nakamura Y, Oka M, Soda H, Shiozawa K, Yoshikawa M, Itoh A, et al: Gefitinib ('Iressa', ZD1839), an epidermal growth factor receptor tyrosine kinase inhibitor, reverses breast cancer resistance protein/ABCG2-mediated drug resistance. Cancer Res 2005; 65: 1541-1546
-
(2005)
Cancer Res
, vol.65
, pp. 1541-1546
-
-
Nakamura, Y.1
Oka, M.2
Soda, H.3
Shiozawa, K.4
Yoshikawa, M.5
Itoh, A.6
-
25
-
-
79952016115
-
Production of cells with targeted integration of gene variants of human ABC transporter for stable and regulated expression using the Flp recombinase system
-
Wakabayashi-Nakao K, Tamura A, Koshiba S, Toyoda Y, Nakagawa H, Ishikawa T: Production of cells with targeted integration of gene variants of human ABC transporter for stable and regulated expression using the Flp recombinase system. Methods Mol Biol 2010; 648: 139-159
-
(2010)
Methods Mol Biol
, Issue.648
, pp. 139-159
-
-
Wakabayashi-Nakao, K.1
Tamura, A.2
Koshiba, S.3
Toyoda, Y.4
Nakagawa, H.5
Ishikawa, T.6
-
26
-
-
34347363131
-
Quantitative SAR analysis and molecular dynamic simulation to functionally validate nonsynonymous polymorphisms of human ABC transporter ABCB1
-
Sakurai A, Onishi Y, Hirano H, Seigneuret M, Obanayama K, Kim G, et al: Quantitative SAR analysis and molecular dynamic simulation to functionally validate nonsynonymous polymorphisms of human ABC transporter ABCB1. Biochemistry 2007; 46: 7678-7693
-
(2007)
Biochemistry
, vol.46
, pp. 7678-7693
-
-
Sakurai, A.1
Onishi, Y.2
Hirano, H.3
Seigneuret, M.4
Obanayama, K.5
Kim, G.6
-
27
-
-
0142106518
-
Simple non-ionpaired high-performance liquid chromatographic method for simultaneous quantitation of carboxylate and lactone forms of 14 new camptothecin derivatives
-
Sano K, Yoshikawa M, Hayasaka S, Satake K, Ikegami Y, Yoshida H, et al: Simple non-ionpaired high-performance liquid chromatographic method for simultaneous quantitation of carboxylate and lactone forms of 14 new camptothecin derivatives. J Chromatogr B Analyt Technol Biomed Life Sci 2003; 795: 25-34
-
(2003)
J Chromatogr B Analyt Technol Biomed Life Sci
, vol.795
, pp. 25-34
-
-
Sano, K.1
Yoshikawa, M.2
Hayasaka, S.3
Satake, K.4
Ikegami, Y.5
Yoshida, H.6
-
28
-
-
1642323740
-
Protein kinase inhibitors: Insights into drug design from structure
-
Noble ME, Endicott JA, Johnson LN: Protein kinase inhibitors: Insights into drug design from structure. Science 2004; 303: 1800-1805
-
(2004)
Science
, vol.303
, pp. 1800-1805
-
-
Noble, M.E.1
Endicott, J.A.2
Johnson, L.N.3
-
29
-
-
0037392444
-
Issues and progress with protein kinase inhibitors for cancer treatment
-
Danceyand J, Sausville EA. Issues and progress with protein kinase inhibitors for cancer treatment. Nat Rev Drug Discov 2003; 2: 296-313
-
(2003)
Nat Rev Drug Discov
, vol.2
, pp. 296-313
-
-
Danceyand, J.1
Sausville, E.A.2
-
30
-
-
26444594410
-
Clinical pharmacogenetics of irinotecan (CPT-11). A comprehensive review article addressing the genetic polymorphisms of UDP-glucuronosyltransferase gene and irinotecan-induced adverse reactions
-
Ando Y, Hasegawa Y: Clinical pharmacogenetics of irinotecan (CPT-11). A comprehensive review article addressing the genetic polymorphisms of UDP-glucuronosyltransferase gene and irinotecan-induced adverse reactions. Drug Metab Rev 2005; 37: 565-574
-
(2005)
Drug Metab Rev
, vol.37
, pp. 565-574
-
-
Ando, Y.1
Hasegawa, Y.2
-
31
-
-
4143101374
-
Relevance of different UGT1A1 polymorphisms in irinotecan- induced toxicity: A molecular and clinical study of 75 patients
-
Rouits E, Boisdron-Celle M, Dumont A, Guerin O, Morel A, Gamelin E: Relevance of different UGT1A1 polymorphisms in irinotecan- induced toxicity: A molecular and clinical study of 75 patients. Clin Cancer Res 2004; 10: 5151-5159
-
(2004)
Clin Cancer Res
, vol.10
, pp. 5151-5159
-
-
Rouits, E.1
Boisdron-Celle, M.2
Dumont, A.3
Guerin, O.4
Morel, A.5
Gamelin, E.6
-
32
-
-
0036025450
-
UGT1A1 28 polymorphism as a determinant of irinotecan disposition and adverse reactions
-
Iyer L, Das S, Janisch L, Wen M, Ramirez J, Karrison T, et al: UGT1A1 . 28 polymorphism as a determinant of irinotecan disposition and adverse reactions. Pharmacogenomics J 2002; 2: 43-47
-
(2002)
Pharmacogenomics J
, vol.2
, pp. 43-47
-
-
Iyer, L.1
Das, S.2
Janisch, L.3
Wen, M.4
Ramirez, J.5
Karrison, T.6
-
33
-
-
2342459714
-
Genetic variants in the UDP-glucuronosyltransferase 1A1 gene predict the risk of severe neutropenia of irinotecan
-
Innocenti F, Undevia SD, Iyer L, Chen PX, Das S, Kocherginsky M, et al: Genetic variants in the UDP-glucuronosyltransferase 1A1 gene predict the risk of severe neutropenia of irinotecan. J Clin Oncol 2004; 22: 1382-1388
-
(2004)
J Clin Oncol
, vol.22
, pp. 1382-1388
-
-
Innocenti, F.1
Undevia, S.D.2
Iyer, L.3
Chen, P.X.4
Das, S.5
Kocherginsky, M.6
-
34
-
-
4344632633
-
UGT1A1 gene variations and irinotecan treatment in patients with metastatic colorectal cancer
-
Marcuello E, Altes A, Menoyo A, Del Rio E, Gomez-Pardo M, Baiget M: UGT1A1 gene variations and irinotecan treatment in patients with metastatic colorectal cancer. Br J Cancer 2004; 91: 678-682
-
(2004)
Br J Cancer
, vol.91
, pp. 678-682
-
-
Marcuello, E.1
Altes, A.2
Menoyo, A.3
Del Rio, E.4
Gomez-Pardo, M.5
Baiget, M.6
-
35
-
-
21944434407
-
Genetic polymorphism in the phenobarbital-responsive enhancer module of the UDP-glucuronosyltransferase 1A1 gene and irinotecan toxicity
-
Kitagawa C, Ando M, Ando Y, Sekido Y, Wakai K, Imaizumi K, et al: Genetic polymorphism in the phenobarbital-responsive enhancer module of the UDP-glucuronosyltransferase 1A1 gene and irinotecan toxicity. Pharmacogenet Genomics 2005; 15: 35-41
-
(2005)
Pharmacogenet Genomics
, vol.15
, pp. 35-41
-
-
Kitagawa, C.1
Ando, M.2
Ando, Y.3
Sekido, Y.4
Wakai, K.5
Imaizumi, K.6
-
36
-
-
52849098688
-
Gefitinib increases serum concentration of oral irinotecan and SN-38 without increasing the biliary concentration of SN-38 in rats
-
Nakamura Y, Satake K, Sano K, Ito A, Yoshikawa M, Ikegami Y, et al: Gefitinib increases serum concentration of oral irinotecan and SN-38 without increasing the biliary concentration of SN-38 in rats. Chemotherapy 2008; 54: 485-491
-
(2008)
Chemotherapy
, vol.54
, pp. 485-491
-
-
Nakamura, Y.1
Satake, K.2
Sano, K.3
Ito, A.4
Yoshikawa, M.5
Ikegami, Y.6
-
37
-
-
76749168084
-
Tyrosine kinase inhibitor enhances the bioavailability of oral irinotecan in pediatric patients with refractory solid tumors
-
Furman WL, Navid F, Daw NC, McCarville MB, McGregor LM, Spunt SL, et al: Tyrosine kinase inhibitor enhances the bioavailability of oral irinotecan in pediatric patients with refractory solid tumors. J Clin Oncol 2009; 27: 4599-4604
-
(2009)
J Clin Oncol
, vol.27
, pp. 4599-4604
-
-
Furman, W.L.1
Navid, F.2
Daw, N.C.3
McCarville, M.B.4
McGregor, L.M.5
Spunt, S.L.6
-
38
-
-
84865058541
-
A phase I clinical trial of irinotecan and carboplatin in patients with extensive stage small cell lung cancer
-
Crabb SJ, Bradbury J, Nolan L, Selman D, Muthuramalingam SR, Cave J, et al: A phase I clinical trial of irinotecan and carboplatin in patients with extensive stage small cell lung cancer. Chemotherapy 2012; 58: 257-263
-
(2012)
Chemotherapy
, Issue.58
, pp. 257-263
-
-
Crabb, S.J.1
Bradbury, J.2
Nolan, L.3
Selman, D.4
Muthuramalingam, S.R.5
Cave, J.6
|