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Volumn 15, Issue 8, 2004, Pages 773-778

Enhanced therapeutic efficacy of a novel liposome-based formulation of SN-38 against human tumor models in SCID mice

Author keywords

CPT 11; Cytotoxicity; Human tumor xenografts; Liposome based formulation; SN 38

Indexed keywords

7 ETHYL 10 HYDROXYCAMPTOTHECIN; IRINOTECAN; LIPOSOME; PRODRUG; SOLVENT; SULFORHODAMINE B;

EID: 4644310318     PISSN: 09594973     EISSN: None     Source Type: Journal    
DOI: 10.1097/00001813-200409000-00006     Document Type: Article
Times cited : (39)

References (27)
  • 1
    • 0027194943 scopus 로고
    • Phase II study of CPT-11, a new camptothecin derivative, in metastatic colorectal cancer
    • Shimada Y, Yoshino M, Wakui A, et al. Phase II study of CPT-11, a new camptothecin derivative, in metastatic colorectal cancer. J Clin Oncol 1993; 11:909-913.
    • (1993) J Clin Oncol , vol.11 , pp. 909-913
    • Shimada, Y.1    Yoshino, M.2    Wakui, A.3
  • 2
    • 0037316549 scopus 로고    scopus 로고
    • Three-week schedule of irinotecan and cisplatin in advanced non-small cell lung cancer: A multicenter phase II study
    • Cardenal F, Domine M, Massuti B, et al. Three-week schedule of irinotecan and cisplatin in advanced non-small cell lung cancer: a multicenter phase II study. Lung Cancer 2003; 39:201-207.
    • (2003) Lung Cancer , vol.39 , pp. 201-207
    • Cardenal, F.1    Domine, M.2    Massuti, B.3
  • 4
    • 0037440035 scopus 로고    scopus 로고
    • Phase II trial of irinotecan in patients with metastatic epithelial ovarian cancer or peritoneal cancer
    • Bodurka DC, Levenback C, Wolf JK, et al. Phase II trial of irinotecan in patients with metastatic epithelial ovarian cancer or peritoneal cancer. J Clin Oncol 2003; 21:291-297.
    • (2003) J Clin Oncol , vol.21 , pp. 291-297
    • Bodurka, D.C.1    Levenback, C.2    Wolf, J.K.3
  • 5
    • 0022340594 scopus 로고
    • Camptothecin induces protein-linked DNA breaks via mammalian DNA topoisomerase I
    • Hsiang YH, Hertzberg R, Hecht S, Lui LF. Camptothecin induces protein-linked DNA breaks via mammalian DNA topoisomerase I. J Biol Chem 1985; 260:14873-14878.
    • (1985) J Biol Chem , vol.260 , pp. 14873-14878
    • Hsiang, Y.H.1    Hertzberg, R.2    Hecht, S.3    Lui, L.F.4
  • 6
    • 0024420685 scopus 로고
    • Arrest of DNA replication by drug-stabilized topoisomerase I-DNA cleavable complexes as a mechanism of cell killing by Camptothecin
    • Hsiang YH, Lihou MG, Lui LF. Arrest of DNA replication 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    Lui, L.F.3
  • 7
    • 0024388737 scopus 로고
    • Differential requirement of DNA replication for the cytotoxicity of DNA-topoisomerase I and II inhibitors in Chinese hamster DC3F cells
    • Holm C, Covey JM, Kerrigan D, Pommier Y. Differential requirement of DNA replication for the cytotoxicity of DNA-topoisomerase I and II inhibitors in Chinese hamster DC3F cells. Cancer Res 1989; 49:6365-6368.
    • (1989) Cancer Res , vol.49 , pp. 6365-6368
    • Holm, C.1    Covey, J.M.2    Kerrigan, D.3    Pommier, Y.4
  • 8
    • 0030863434 scopus 로고    scopus 로고
    • Bioactivation of the anticancer agent CPT-11 to SN-38 by human hepatic microsomal carboxylesterases and the in vitro assessment of potential drug interactions
    • Slatter JG, Su P, Sams JP, Schaaf LJ, Wienkers LC. Bioactivation of the anticancer agent CPT-11 to SN-38 by human hepatic microsomal carboxylesterases and the in vitro assessment of potential drug interactions. Drug Metab Disp 1997; 25:1157-1164.
    • (1997) Drug Metab Disp , vol.25 , pp. 1157-1164
    • Slatter, J.G.1    Su, P.2    Sams, J.P.3    Schaaf, L.J.4    Wienkers, L.C.5
  • 10
    • 0035569857 scopus 로고    scopus 로고
    • Improved safety, pharmacokinetics and therapeutic efficacy profiles of a novel liposomal formulation of mitoxantrone
    • Gokhale PC, Pei J, Zhang C, Ahmad I, Rahman A, Kasid U. Improved safety, pharmacokinetics and therapeutic efficacy profiles of a novel liposomal formulation of mitoxantrone. Anticancer Res 2001; 21:3313-3321.
    • (2001) Anticancer Res , vol.21 , pp. 3313-3321
    • Gokhale, P.C.1    Pei, J.2    Zhang, C.3    Ahmad, I.4    Rahman, A.5    Kasid, U.6
  • 11
    • 0842279809 scopus 로고
    • Liposome formulations with prolonged circulation time in blood and enhanced uptake by tumors
    • Gabizon A, Papahadjopoulos D. Liposome formulations with prolonged circulation time in blood and enhanced uptake by tumors. Proc Natl Acad Sci USA 1988; 85:6949-6953.
    • (1988) Proc Natl Acad Sci USA , vol.85 , pp. 6949-6953
    • Gabizon, A.1    Papahadjopoulos, D.2
  • 12
    • 0035164058 scopus 로고    scopus 로고
    • A comparison of liposomal formulations of doxorubicin with drug administered in free form: Changing toxicity profiles
    • Waterhouse DN, Tardi PG, Mayer LD, Bally MB. A comparison of liposomal formulations of doxorubicin with drug administered in free form: changing toxicity profiles. Drug Saf 2001; 24:903-920.
    • (2001) Drug Saf , vol.24 , pp. 903-920
    • Waterhouse, D.N.1    Tardi, P.G.2    Mayer, L.D.3    Bally, M.B.4
  • 13
    • 0346392116 scopus 로고    scopus 로고
    • Development and characterization of a novel liposome-based formulation of SN-38
    • Zhang JA, Xuan T, Parmar M, Ma L, Ugwu S, Ali S, Ahmad I. Development and characterization of a novel liposome-based formulation of SN-38. Int J Pharm 2004; 270:93-107.
    • (2004) Int J Pharm , vol.270 , pp. 93-107
    • Zhang, J.A.1    Xuan, T.2    Parmar, M.3    Ma, L.4    Ugwu, S.5    Ali, S.6    Ahmad, I.7
  • 14
    • 12344256836 scopus 로고    scopus 로고
    • A simple and sensitive LC/MS/MS assay for 7-ethyl-10-hydroxycamptothecin (SN-38) in mouse plasma and tissues:application to pharmacokinetic study of liposome entrapped SN-38 (LE-SN38)
    • in press
    • Khan S, Ahmad A, Guo W, Wang Y-F, Abu-Qare A, Ahmad I. A simple and sensitive LC/MS/MS assay for 7-ethyl-10-hydroxycamptothecin (SN-38) in mouse plasma and tissues:application to pharmacokinetic study of liposome entrapped SN-38 (LE-SN38). J Pharmac Biomed Anal 2004; in press.
    • (2004) J Pharmac Biomed Anal
    • Khan, S.1    Ahmad, A.2    Guo, W.3    Wang, Y.-F.4    Abu-Qare, A.5    Ahmad, I.6
  • 15
    • 0025341331 scopus 로고
    • New colorimetric cytotoxicity assay for anticancer-drug screening
    • Skehan P, Storeng R, Scudiero D, et al. New colorimetric cytotoxicity assay for anticancer-drug screening. J Natl Cancer Inst 1990; 82: 1107-1112.
    • (1990) J Natl Cancer Inst , vol.82 , pp. 1107-1112
    • Skehan, P.1    Storeng, R.2    Scudiero, D.3
  • 16
    • 0030055094 scopus 로고    scopus 로고
    • Current perspectives on camptothecins in cancer treatment
    • Dancey J, Eisenhauer EA. Current perspectives on camptothecins in cancer treatment. Br J Cancer 1996; 74:327-328.
    • (1996) Br J Cancer , vol.74 , pp. 327-328
    • Dancey, J.1    Eisenhauer, E.A.2
  • 17
    • 0032411767 scopus 로고    scopus 로고
    • Irinotecan: A new antineoplastic agent for the management of colorectal cancer
    • Cersosimo RJ. Irinotecan: a new antineoplastic agent for the management of colorectal cancer. Ann Pharmacother 1998; 32:1324-1333.
    • (1998) Ann Pharmacother , vol.32 , pp. 1324-1333
    • Cersosimo, R.J.1
  • 18
    • 0034231594 scopus 로고    scopus 로고
    • Effective prodrug liposome and conversion to active metabolite
    • Sadzuka Y. Effective prodrug liposome and conversion to active metabolite. Curr Drug Metab 2000; 1:31-48.
    • (2000) Curr Drug Metab , vol.1 , pp. 31-48
    • Sadzuka, Y.1
  • 19
    • 0024445654 scopus 로고
    • Some pharmacological properties of a new antitumor drug, CPT-11, in isolated muscle preparations
    • Takayanagi I, Koike K, Tagawa M, Mitsuhashi E. Some pharmacological properties of a new antitumor drug, CPT-11, in isolated muscle preparations. Gen Pharmacol 1989; 20:763-776.
    • (1989) Gen Pharmacol , vol.20 , pp. 763-776
    • Takayanagi, I.1    Koike, K.2    Tagawa, M.3    Mitsuhashi, E.4
  • 20
    • 0032926512 scopus 로고    scopus 로고
    • CPT-11 converting carboxylesterase and topoisomerase I activities in tumor and normal colon and liver tissues
    • Guichard S, Terret C, Hennebelle I, et al. CPT-11 converting carboxylesterase and topoisomerase I activities in tumor and normal colon and liver tissues. Br J Cancer 1999; 80:364-370.
    • (1999) Br J Cancer , vol.80 , pp. 364-370
    • Guichard, S.1    Terret, C.2    Hennebelle, I.3
  • 21
    • 0034162687 scopus 로고    scopus 로고
    • Characterization of CPT-11 hydrolysis by human liver carboxylesterase isoforms hCE-1 and hCE-2
    • Humerickhouse R, Lohrbach K, Li L, Bosron WF, Dolan ME. Characterization of CPT-11 hydrolysis by human liver carboxylesterase isoforms hCE-1 and hCE-2. Cancer Res 2000; 60:1189-1192.
    • (2000) Cancer Res , vol.60 , pp. 1189-1192
    • Humerickhouse, R.1    Lohrbach, K.2    Li, L.3    Bosron, W.F.4    Dolan, M.E.5
  • 22
    • 0037829150 scopus 로고    scopus 로고
    • Intracellular conversion of irinotecan to its active form, SN-38, by native carboxylesterase in human non-small cell lung cancer
    • Ohtsuka K, Kameyama M, Kanetoshi A, Fujimoto T, Takaoka K, Shida AY. Intracellular conversion of irinotecan to its active form, SN-38, by native carboxylesterase in human non-small cell lung cancer. Lung Cancer 2003; 41:187-188.
    • (2003) Lung Cancer , vol.41 , pp. 187-188
    • Ohtsuka, K.1    Kameyama, M.2    Kanetoshi, A.3    Fujimoto, T.4    Takaoka, K.5    Shida, A.Y.6
  • 23
    • 0034892379 scopus 로고    scopus 로고
    • Clinical pharmacokinetics and metabolism of irinotecan (CPT-11)
    • Mathijssen RH, van Alphen RJ, Verweij J, et al. Clinical pharmacokinetics and metabolism of irinotecan (CPT-11). Clin Cancer Res 2001; 7: 2182-2194.
    • (2001) Clin Cancer Res , vol.7 , pp. 2182-2194
    • Mathijssen, R.H.1    Van Alphen, R.J.2    Verweij, J.3
  • 25
    • 0033809224 scopus 로고    scopus 로고
    • New highly lipophilic camptothecin BNP1350 is an effective drug in experimental human cancer
    • Van Hattum AH, Pinedo HM, Schluper HM, Hausheer FH, Boven E. New highly lipophilic camptothecin BNP1350 is an effective drug in experimental human cancer. Int J Cancer 2000; 88:260-266.
    • (2000) Int J Cancer , vol.88 , pp. 260-266
    • Van Hattum, A.H.1    Pinedo, H.M.2    Schluper, H.M.3    Hausheer, F.H.4    Boven, E.5
  • 26
    • 0025996996 scopus 로고
    • 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
  • 27
    • 0031046059 scopus 로고    scopus 로고
    • CPT-11 in human colon-cancer cell lines and xenografts: Characterization of cellular sensitivity determinants
    • Jansen WJ, Zwart B, Hulscher ST, Giaccone G, Pinedo HM, Boven E. CPT-11 in human colon-cancer cell lines and xenografts: characterization of cellular sensitivity determinants. Int J Cancer 1997; 70:335-340.
    • (1997) Int J Cancer , vol.70 , pp. 335-340
    • Jansen, W.J.1    Zwart, B.2    Hulscher, S.T.3    Giaccone, G.4    Pinedo, H.M.5    Boven, E.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.