메뉴 건너뛰기




Volumn 54, Issue 6, 2008, Pages 485-491

Gefitinib increases serum concentrations of oral irinotecan and SN-38 without increasing the biliary concentration of SN-38 in rats

Author keywords

ABCG2 BCRP; EGFR inhibitor; Oral chemotherapy; Topoisomerase I inhibitor

Indexed keywords

7 ETHYL 10 HYDROXYCAMPTOTHECIN; GEFITINIB; GLUCURONIDE; IRINOTECAN;

EID: 52849098688     PISSN: 00093157     EISSN: None     Source Type: Journal    
DOI: 10.1159/000159625     Document Type: Article
Times cited : (4)

References (26)
  • 1
    • 0031859489 scopus 로고    scopus 로고
    • Oral chemotherapy: Rationale and future directions
    • DeMario MD, Ratain MJ: Oral chemotherapy: rationale and future directions. J Clin Oncol 1998;16:2557-2567.
    • (1998) J Clin Oncol , vol.16 , pp. 2557-2567
    • DeMario, M.D.1    Ratain, M.J.2
  • 2
    • 0031017851 scopus 로고    scopus 로고
    • Patient preferences for oral versus intravenous palliative chemotherapy
    • Liu G, Franssen E, Fitch MI, Warner E: Patient preferences for oral versus intravenous palliative chemotherapy. J Clin Oncol 1997;15:110-115.
    • (1997) J Clin Oncol , vol.15 , pp. 110-115
    • Liu, G.1    Franssen, E.2    Fitch, M.I.3    Warner, E.4
  • 3
    • 36049012360 scopus 로고    scopus 로고
    • Dihydropyrimidine dehydrogenase activity during long-term adjuvant treatment with oral uracil and tegafur for colorectal cancer
    • Sadahiro S, Suzuki T, Maeda Y, Ishikawa K, Tanaka Y, Yasuda S, Kamijo A, Makuuchi H, Murayama C: Dihydropyrimidine dehydrogenase activity during long-term adjuvant treatment with oral uracil and tegafur for colorectal cancer. Chemotherapy 2007;53:442-445.
    • (2007) Chemotherapy , vol.53 , pp. 442-445
    • Sadahiro, S.1    Suzuki, T.2    Maeda, Y.3    Ishikawa, K.4    Tanaka, Y.5    Yasuda, S.6    Kamijo, A.7    Makuuchi, H.8    Murayama, C.9
  • 4
    • 0030444901 scopus 로고    scopus 로고
    • Interpatient variability in bioavailability is related to the extent of absorption: Implications for bioavailability and bioequivalence studies
    • Hellriegel ET, Bjornsson TD, Hauck WW: Interpatient variability in bioavailability is related to the extent of absorption: implications for bioavailability and bioequivalence studies. Clin Pharmacol Ther 1996;60:601-607.
    • (1996) Clin Pharmacol Ther , vol.60 , pp. 601-607
    • Hellriegel, E.T.1    Bjornsson, T.D.2    Hauck, W.W.3
  • 5
    • 0036909078 scopus 로고    scopus 로고
    • Improvement of oral drug treatment by temporary inhibition of drug transporters and/or cytochrome P450 in the gastrointestinal tract and liver: An overview
    • Kruijtzer CM, Beijnen JH, Schellens JH: Improvement of oral drug treatment by temporary inhibition of drug transporters and/or cytochrome P450 in the gastrointestinal tract and liver: an overview. Oncologist 2002;7:516-530.
    • (2002) Oncologist , vol.7 , pp. 516-530
    • Kruijtzer, C.M.1    Beijnen, J.H.2    Schellens, J.H.3
  • 6
    • 24944449437 scopus 로고    scopus 로고
    • Modulation of oral drug bioavailability: From preclinical mechanism to therapeutic application
    • Kuppens IE, Breedveld P, Beijnen JH, JH Schellens: Modulation of oral drug bioavailability: from preclinical mechanism to therapeutic application. Cancer Invest 2005;23:443-464.
    • (2005) Cancer Invest , vol.23 , pp. 443-464
    • Kuppens, I.E.1    Breedveld, P.2    Beijnen, J.H.3    Schellens, J.H.4
  • 7
    • 0024432823 scopus 로고
    • Identification of the multidrug resistance-related P-glycoprotein as a cyclosporine binding protein
    • Foxwell BM, Mackie A, Ling V, Ryffel B: Identification of the multidrug resistance-related P-glycoprotein as a cyclosporine binding protein. Mol Pharmacol 1989;36:543-546.
    • (1989) Mol Pharmacol , vol.36 , pp. 543-546
    • Foxwell, B.M.1    Mackie, A.2    Ling, V.3    Ryffel, B.4
  • 11
    • 5644264888 scopus 로고    scopus 로고
    • Stewart CF, Leggas M, Schuetz JD, Panetta JC, Cheshire PJ, Peterson J, Daw N, Jenkins JJ 3 rd , Gilbertson R, Germain GS, Harwood FC, Houghton PJ: Gefitinib enhances the antitumor activity and oral bioavailability of irinotecan in mice. Cancer Res 2004;64:7491-7499.
    • Stewart CF, Leggas M, Schuetz JD, Panetta JC, Cheshire PJ, Peterson J, Daw N, Jenkins JJ 3 rd , Gilbertson R, Germain GS, Harwood FC, Houghton PJ: Gefitinib enhances the antitumor activity and oral bioavailability of irinotecan in mice. Cancer Res 2004;64:7491-7499.
  • 15
    • 0033429542 scopus 로고    scopus 로고
    • Camptothecin resistance: Role of the ATP-binding cassette (ABC), mitoxantrone-resistance half-transporter (MXR), and potential for glucuronidation in MXR-expressing cells
    • Brangi M, Litman T, Ciotti M, Nishiyama K, Kohlhagen G, Takimoto C, Robey R, Pommier Y, Fojo T, Bates SE: Camptothecin resistance: role of the ATP-binding cassette (ABC), mitoxantrone-resistance half-transporter (MXR), and potential for glucuronidation in MXR-expressing cells. Cancer Res 1999;59:5938-5946.
    • (1999) Cancer Res , vol.59 , pp. 5938-5946
    • Brangi, M.1    Litman, T.2    Ciotti, M.3    Nishiyama, K.4    Kohlhagen, G.5    Takimoto, C.6    Robey, R.7    Pommier, Y.8    Fojo, T.9    Bates, S.E.10
  • 17
    • 0345734200 scopus 로고    scopus 로고
    • Synergistic interaction between the EGFR tyrosine kinase inhibitor gefitinib ('Iressa') and the DNA topoisomerase I inhibitor CPT-11 (irinotecan) in human colorectal cancer cells
    • Koizumi F, Kanzawa F, Ueda Y, Koh Y, Tsukiyama S, Taguchi F, Tamura T, Saijo N, Nishio K: Synergistic interaction between the EGFR tyrosine kinase inhibitor gefitinib ('Iressa') and the DNA topoisomerase I inhibitor CPT-11 (irinotecan) in human colorectal cancer cells. Int J Cancer 2004;108:464-472.
    • (2004) Int J Cancer , vol.108 , pp. 464-472
    • Koizumi, F.1    Kanzawa, F.2    Ueda, Y.3    Koh, Y.4    Tsukiyama, S.5    Taguchi, F.6    Tamura, T.7    Saijo, N.8    Nishio, K.9
  • 19
    • 0030741008 scopus 로고    scopus 로고
    • Simultaneous determination of the lactone and carboxylate forms of 7-ethyl-10-hydroxycamptothecin (SN-38), the active metabolite of irinotecan (CPT-11), in rat plasma by high performance liquid chromatography
    • Kaneda N, Hosokawa Y, Yokokura T: Simultaneous determination of the lactone and carboxylate forms of 7-ethyl-10-hydroxycamptothecin (SN-38), the active metabolite of irinotecan (CPT-11), in rat plasma by high performance liquid chromatography. Biol Pharm Bull 1997;20:815-819.
    • (1997) Biol Pharm Bull , vol.20 , pp. 815-819
    • Kaneda, N.1    Hosokawa, Y.2    Yokokura, T.3
  • 20
    • 46449133480 scopus 로고    scopus 로고
    • Kars MD, I?eri OD, Gunduz U, Molnar J: Reversal of multidrug resistance by synthetic and natural compounds in drug-resistant MCF-7 cell lines. Chemotherapy 2008;54:194-200.
    • Kars MD, I?eri OD, Gunduz U, Molnar J: Reversal of multidrug resistance by synthetic and natural compounds in drug-resistant MCF-7 cell lines. Chemotherapy 2008;54:194-200.
  • 24
    • 0027242140 scopus 로고
    • Relationship between development of diarrhea and the concentration of SN-38, an active metabolite of CPT-11, in the intestine and the blood plasma of athymic mice following intraperitoneal administration of CPT-11
    • Araki E, Ishikawa M, Iigo M, Koide T, Itabashi M, Hoshi A: Relationship between development of diarrhea and the concentration of SN-38, an active metabolite of CPT-11, in the intestine and the blood plasma of athymic mice following intraperitoneal administration of CPT-11. Jpn J Cancer Res 1993;84:697-702.
    • (1993) Jpn J Cancer Res , vol.84 , pp. 697-702
    • Araki, E.1    Ishikawa, M.2    Iigo, M.3    Koide, T.4    Itabashi, M.5    Hoshi, A.6
  • 26
    • 28144436318 scopus 로고    scopus 로고
    • Gefitinib (Iressa) inhibits the CYP3A4-mediated formation of 7-ethyl-10-(4-amino-1-piperidino)carbonyl oxycamptothecin but activates that of 7-ethyl-10-[4-N-(5-aminopentanoic acid)-1-piperidino] carbonyloxycamptothecin from irinotecan
    • Fujita K, Ando Y, Narabayashi M, Miya T, Nagashima F, Yamamoto W, Kodama K, Araki K, Endo H, Sasaki Y: Gefitinib (Iressa) inhibits the CYP3A4-mediated formation of 7-ethyl-10-(4-amino-1-piperidino)carbonyl oxycamptothecin but activates that of 7-ethyl-10-[4-N-(5-aminopentanoic acid)-1-piperidino] carbonyloxycamptothecin from irinotecan. Drug Metab Dispos 2005;33:1785-1790.
    • (2005) Drug Metab Dispos , vol.33 , pp. 1785-1790
    • Fujita, K.1    Ando, Y.2    Narabayashi, M.3    Miya, T.4    Nagashima, F.5    Yamamoto, W.6    Kodama, K.7    Araki, K.8    Endo, H.9    Sasaki, Y.10


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.