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Volumn 25, Issue 6, 1997, Pages 647-672

Antiprogestin pharmacodynamics, pharmacokinetics, and metabolism: Implications for their long-term use

Author keywords

Antiprogestins; Cytochrome P450 3A4; Drug drug interactions; Lilopristone; Mifepristone; Onapristone; P glycoprotein; Receptor binding; Satutable protein binding

Indexed keywords

ANTIGESTAGEN; LILOPRISTONE; MIFEPRISTONE; ONAPRISTONE;

EID: 0031403618     PISSN: 0090466X     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1025725716343     Document Type: Review
Times cited : (16)

References (134)
  • 4
    • 0023624268 scopus 로고
    • Synthesis of antiprogestational steroids
    • R. Wiechert and G. Neef. Synthesis of antiprogestational steroids. J. Steroid Biochem. 27:851-858 (1987).
    • (1987) J. Steroid Biochem. , vol.27 , pp. 851-858
    • Wiechert, R.1    Neef, G.2
  • 6
    • 0028040033 scopus 로고
    • Termination of early pregnancy with ZK 98.734: Pharmacokinetic behaviour and clinical effect
    • M. L. Swahn, L. Kovacs, S. Z. Cekan, A. R. Aedo, and P. Westlun. Termination of early pregnancy with ZK 98.734: pharmacokinetic behaviour and clinical effect. Hum. Reprod. 9:57-63 (1994).
    • (1994) Hum. Reprod. , vol.9 , pp. 57-63
    • Swahn, M.L.1    Kovacs, L.2    Cekan, S.Z.3    Aedo, A.R.4    Westlun, P.5
  • 7
    • 0030066575 scopus 로고    scopus 로고
    • The effects of post-ovulatory administration of onapristone on the development of a secretory endometrium
    • S. T. Cameron, H. O. Critchley, C. H. Buckley, T. Chard, R. W. Kelly, and D. T. Baird. The effects of post-ovulatory administration of onapristone on the development of a secretory endometrium. Hum. Reprod. 11:40-49 (1996).
    • (1996) Hum. Reprod. , vol.11 , pp. 40-49
    • Cameron, S.T.1    Critchley, H.O.2    Buckley, C.H.3    Chard, T.4    Kelly, R.W.5    Baird, D.T.6
  • 8
    • 0023913120 scopus 로고
    • The steroid and thyroid hormone receptor superfamily
    • R. M. Evans. The steroid and thyroid hormone receptor superfamily. Science 240:889-895 (1988).
    • (1988) Science , vol.240 , pp. 889-895
    • Evans, R.M.1
  • 9
    • 0024545638 scopus 로고
    • Gene regulation by steroid hormones
    • M. Beato. Gene regulation by steroid hormones. Cell 56:335-344 (1989).
    • (1989) Cell , vol.56 , pp. 335-344
    • Beato, M.1
  • 10
    • 0026343102 scopus 로고
    • Molecular pathways of steroid receptor action
    • B. W. O'Malley and M. J. Tsai. Molecular pathways of steroid receptor action. Biol. Reprod. 46:163-167 (1992).
    • (1992) Biol. Reprod. , vol.46 , pp. 163-167
    • O'Malley, B.W.1    Tsai, M.J.2
  • 11
    • 0028283503 scopus 로고
    • Molecular mechanisms of action of steroid/thyroid receptor superfamily members
    • M. J. Tsai and B. W. O'Malley. Molecular mechanisms of action of steroid/thyroid receptor superfamily members. Ann. Rev. Biochem. 63:451-486 (1994).
    • (1994) Ann. Rev. Biochem. , vol.63 , pp. 451-486
    • Tsai, M.J.1    O'Malley, B.W.2
  • 13
    • 0002708343 scopus 로고
    • RU 38486: An original multifaceted antihormone in vivo
    • K. Agarwal (ed.), Walter de Gruyter, Berlin
    • D. Philibert. RU 38486: An original multifaceted antihormone in vivo. In K. Agarwal (ed.), Adrenal Steroid Antagonism, Walter de Gruyter, Berlin, 1984, pp. 77-101.
    • (1984) Adrenal Steroid Antagonism , pp. 77-101
    • Philibert, D.1
  • 14
    • 0026726806 scopus 로고
    • Hormone and antihormone induce distinct conformational changes which are central to steroid receptor activation
    • G. F. Allan, X. Leng, S. Y. Tsai, N. L. Weigel, D. P. Edwards, M. J. Tsai, and B. W. O'Malley. Hormone and antihormone induce distinct conformational changes which are central to steroid receptor activation. J. Biol. Chem. 267:19513-19520 (1992).
    • (1992) J. Biol. Chem. , vol.267 , pp. 19513-19520
    • Allan, G.F.1    Leng, X.2    Tsai, S.Y.3    Weigel, N.L.4    Edwards, D.P.5    Tsai, M.J.6    O'Malley, B.W.7
  • 15
    • 0026096890 scopus 로고
    • Two types of antiprogestins identified by their differential action in transcriptionally active extracts from T47D cells
    • L. Klein-Hitpass, A. C. Cato, D. Henderson, and G. U. Ryffel. Two types of antiprogestins identified by their differential action in transcriptionally active extracts from T47D cells. Nucleic Acids Res. 19:1227-1234 (1991).
    • (1991) Nucleic Acids Res. , vol.19 , pp. 1227-1234
    • Klein-Hitpass, L.1    Cato, A.C.2    Henderson, D.3    Ryffel, G.U.4
  • 16
    • 0021610642 scopus 로고
    • New steroids with antiprogestational and antiglucocorticoid activities
    • G. Neef, S. Beier, W. Elger, D. Henderson, and R. Wiechert. New steroids with antiprogestational and antiglucocorticoid activities. Steroids 44:349-372 (1984).
    • (1984) Steroids , vol.44 , pp. 349-372
    • Neef, G.1    Beier, S.2    Elger, W.3    Henderson, D.4    Wiechert, R.5
  • 17
    • 0026786105 scopus 로고
    • Ligands induce conformational changes in the carboxyl-terminus of progesterone receptors which are detected by a site-directed antipeptide monoclonal antibody
    • N. L. Weigel, C. A. Beck, P. A. Estes, P. Prendergast, M. Altmann, K. Christensen, and D. P. Edwards. Ligands induce conformational changes in the carboxyl-terminus of progesterone receptors which are detected by a site-directed antipeptide monoclonal antibody. Mol. Endocrinol. 6:1585-1597 (1992).
    • (1992) Mol. Endocrinol. , vol.6 , pp. 1585-1597
    • Weigel, N.L.1    Beck, C.A.2    Estes, P.A.3    Prendergast, P.4    Altmann, M.5    Christensen, K.6    Edwards, D.P.7
  • 18
    • 0026653659 scopus 로고
    • The mechanism of RU486 antagonism is dependent on the conformation of the carboxy-terminal tail of the human progesterone receptor
    • E. Vegeto, G. F. Allan, W. T. Schrader, M. J. Tsai, D. P. McDonnell, and B. W. O'Malley. The mechanism of RU486 antagonism is dependent on the conformation of the carboxy-terminal tail of the human progesterone receptor. Cell 90:703-713 (1992).
    • (1992) Cell , vol.90 , pp. 703-713
    • Vegeto, E.1    Allan, G.F.2    Schrader, W.T.3    Tsai, M.J.4    McDonnell, D.P.5    O'Malley, B.W.6
  • 19
    • 0024434594 scopus 로고
    • Human progesterone receptor complexed with the antagonist RU 486 binds to hormone response elements in a structurally altered form
    • D. el Ashry, S. A. Onate, S. K. Nordeen, and D. P. Edwards. Human progesterone receptor complexed with the antagonist RU 486 binds to hormone response elements in a structurally altered form. Mol. Endocrinol 3:1545-1558 (1989).
    • (1989) Mol. Endocrinol , vol.3 , pp. 1545-1558
    • El Ashry, D.1    Onate, S.A.2    Nordeen, S.K.3    Edwards, D.P.4
  • 20
    • 0025053671 scopus 로고
    • Agonistic and antagonistic activities of RU486 on the functions of the human progesterone receptor
    • M. E. Meyer, A. Pornon, J. W. Ji, M. T. Bocquel, P. Chambon, and H. Gronemeyer. Agonistic and antagonistic activities of RU486 on the functions of the human progesterone receptor. EMBO J. 9:3923-3932 (1990).
    • (1990) EMBO J. , vol.9 , pp. 3923-3932
    • Meyer, M.E.1    Pornon, A.2    Ji, J.W.3    Bocquel, M.T.4    Chambon, P.5    Gronemeyer, H.6
  • 23
    • 0026559680 scopus 로고
    • Hormone-induced progesterone receptor phosphorylation consists of sequential DNA-independent and DNA-dependent stages: Analysis with zinc finger mutants and the progesterone antagonist ZK98299
    • G. S. Takimoto, D. M. Tasset, A. C. Eppert, and K. B. Horwitz. Hormone-induced progesterone receptor phosphorylation consists of sequential DNA-independent and DNA-dependent stages: analysis with zinc finger mutants and the progesterone antagonist ZK98299. Proc. Natl. Acad. Sci. U.S. 89:3050-3054 (1992).
    • (1992) Proc. Natl. Acad. Sci. U.S. , vol.89 , pp. 3050-3054
    • Takimoto, G.S.1    Tasset, D.M.2    Eppert, A.C.3    Horwitz, K.B.4
  • 25
    • 0030052297 scopus 로고    scopus 로고
    • Two types of antiprogestins have distinct effects on site-specific phosphorylation of human progesterone receptor
    • C. A. Beck, Y. Zhang, N. L. Weigel, and D. P. Edwards. Two types of antiprogestins have distinct effects on site-specific phosphorylation of human progesterone receptor. J. Biol. Chem. 271:1209-1217 (1996).
    • (1996) J. Biol. Chem. , vol.271 , pp. 1209-1217
    • Beck, C.A.1    Zhang, Y.2    Weigel, N.L.3    Edwards, D.P.4
  • 26
    • 0027191140 scopus 로고
    • The progesterone antagonist RU486 acquires agonist activity upon stimulation of cAMP signaling pathways
    • C. A. Beck, N. L. Weigel, M. L. Moyer, S. K. Nordeen, and D. P. Edwards. The progesterone antagonist RU486 acquires agonist activity upon stimulation of cAMP signaling pathways. Proc. Natl. Acad. Sci. U.S. 90:4441-4445 (1993).
    • (1993) Proc. Natl. Acad. Sci. U.S. , vol.90 , pp. 4441-4445
    • Beck, C.A.1    Weigel, N.L.2    Moyer, M.L.3    Nordeen, S.K.4    Edwards, D.P.5
  • 27
    • 0027195589 scopus 로고
    • In vivo evidence against the existence of antiprogestins disrupting receptor binding to DNA
    • K. Delabre, M. A. Guiochon, and E. Milgrom. In vivo evidence against the existence of antiprogestins disrupting receptor binding to DNA. Proc. Natl. Acad. Sci. U.S. 90:4421-4425 (1993).
    • (1993) Proc. Natl. Acad. Sci. U.S. , vol.90 , pp. 4421-4425
    • Delabre, K.1    Guiochon, M.A.2    Milgrom, E.3
  • 28
    • 0025239785 scopus 로고
    • Two distinct estrogen-regulated promoters generate transcripts encoding the two functionally different human progesterone receptor forms A and B
    • P. Kastner, A. Krust, B. Turcotte, U. Stropp, L. Tora, H. Gronemeyer, and P. Chambon. Two distinct estrogen-regulated promoters generate transcripts encoding the two functionally different human progesterone receptor forms A and B. EMBO J. 9:1603-1614 (1990).
    • (1990) EMBO J. , vol.9 , pp. 1603-1614
    • Kastner, P.1    Krust, A.2    Turcotte, B.3    Stropp, U.4    Tora, L.5    Gronemeyer, H.6    Chambon, P.7
  • 29
    • 0030460710 scopus 로고    scopus 로고
    • An aminoterminal truncated progesterone receptor isoform, PRc, enhances progestin-induced transcriptional activity
    • L. L. Wei, P. Hawkins, C. Baker, B. Norris, P. L. Sheridan, and P. G. Quinn. An aminoterminal truncated progesterone receptor isoform, PRc, enhances progestin-induced transcriptional activity. Mol. Endocrinol 10:1379-1387 (1996).
    • (1996) Mol. Endocrinol , vol.10 , pp. 1379-1387
    • Wei, L.L.1    Hawkins, P.2    Baker, C.3    Norris, B.4    Sheridan, P.L.5    Quinn, P.G.6
  • 30
    • 0024524385 scopus 로고
    • The contribution of the N- and C-terminal regions of steroid receptors to activation of transcription is both receptor and cell-specific
    • M. T. Bocquel, V. Kumar, C. Stricker, P. Chambon, and H. Gronemeyer. The contribution of the N- and C-terminal regions of steroid receptors to activation of transcription is both receptor and cell-specific. Nucleic Acids Res. 17:2581-2595 (1989).
    • (1989) Nucleic Acids Res. , vol.17 , pp. 2581-2595
    • Bocquel, M.T.1    Kumar, V.2    Stricker, C.3    Chambon, P.4    Gronemeyer, H.5
  • 31
    • 0027156480 scopus 로고
    • Antagonist-occupied human progesterone receptors bound to DNA are functionally switched to transcriptional agonist by cAMP
    • C. A. Sartorius, L. Tung, G. S. Takimoto, and K. B. Horwitz. Antagonist-occupied human progesterone receptors bound to DNA are functionally switched to transcriptional agonist by cAMP. J. Biol. Chem. 268:9262-9266 (1993).
    • (1993) J. Biol. Chem. , vol.268 , pp. 9262-9266
    • Sartorius, C.A.1    Tung, L.2    Takimoto, G.S.3    Horwitz, K.B.4
  • 32
    • 0028026693 scopus 로고
    • New T47D breast cancer cell lines for the independent study of progesterone B- and A-receptors: Only antiprogestin-occupied B-receptors are switched to transcriptional agonists by cAMP
    • C. A. Sartorius, S. D. Groshong, L. A. Miller, R. L. Powell, L. Tung, G. S. Takimoto, and K. B. Horwitz. New T47D breast cancer cell lines for the independent study of progesterone B- and A-receptors: Only antiprogestin-occupied B-receptors are switched to transcriptional agonists by cAMP. Cancer Res. 54:3868-3877 (1994).
    • (1994) Cancer Res. , vol.54 , pp. 3868-3877
    • Sartorius, C.A.1    Groshong, S.D.2    Miller, L.A.3    Powell, R.L.4    Tung, L.5    Takimoto, G.S.6    Horwitz, K.B.7
  • 33
    • 0030998328 scopus 로고    scopus 로고
    • The partial agonist activity of antagonist-occupied steroid receptors is controlled by a novel hinge domain-binding coactivator L7/SPA and the corepressors N-CoR and SMRT
    • T. A. Jackson, J. K. Richer, D. L. Bain, G. S. Takimoto, L. Tung, and K. B. Horwitz. The partial agonist activity of antagonist-occupied steroid receptors is controlled by a novel hinge domain-binding coactivator L7/SPA and the corepressors N-CoR and SMRT. Mol. Endocrinol. 11:693-705 (1997).
    • (1997) Mol. Endocrinol. , vol.11 , pp. 693-705
    • Jackson, T.A.1    Richer, J.K.2    Bain, D.L.3    Takimoto, G.S.4    Tung, L.5    Horwitz, K.B.6
  • 35
    • 0027220012 scopus 로고
    • Latent agonist activity of the steroid antagonist, RU486, is unmasked in cells treated with activators of protein kinase A
    • S. K. Nordeen, B. J. Bona, and M. L. Moyer. Latent agonist activity of the steroid antagonist, RU486, is unmasked in cells treated with activators of protein kinase A. Mol. Endocrinol. 7:731-742 (1993).
    • (1993) Mol. Endocrinol. , vol.7 , pp. 731-742
    • Nordeen, S.K.1    Bona, B.J.2    Moyer, M.L.3
  • 36
    • 0028799426 scopus 로고
    • Influence of hormone antagonists on chromatin remodeling and transcription factor binding to the mouse mammary tumor virus promoter in vivo
    • J. S. Mymryk and T. K. Archer. Influence of hormone antagonists on chromatin remodeling and transcription factor binding to the mouse mammary tumor virus promoter in vivo. Mol. Endocrinol. 9:1825-1834 (1995).
    • (1995) Mol. Endocrinol. , vol.9 , pp. 1825-1834
    • Mymryk, J.S.1    Archer, T.K.2
  • 37
    • 0028283157 scopus 로고
    • RU486 exerts antiestrogenic activities through a novel progesterone receptor A form-mediated mechanism
    • D. P. McDonnell and M. E. Goldman. RU486 exerts antiestrogenic activities through a novel progesterone receptor A form-mediated mechanism. J. Biol. Chem. 269:11945-11949 (1994).
    • (1994) J. Biol. Chem. , vol.269 , pp. 11945-11949
    • McDonnell, D.P.1    Goldman, M.E.2
  • 38
    • 0004052583 scopus 로고
    • McGraw-Hill, New York
    • N. Applezweig. Steroid Drugs, McGraw-Hill, New York, 1962, pp. 194-195.
    • (1962) Steroid Drugs , pp. 194-195
    • Applezweig, N.1
  • 39
    • 0010945362 scopus 로고
    • RU 486 - A decade on today and tomorrow
    • M. Donaldson, L. Dorflinger, S. S. Brown, and L. Z. Benet (eds.), National Academy Press, Washington, DC
    • E. E. Baulieu. RU 486 - A decade on today and tomorrow. In M. Donaldson, L. Dorflinger, S. S. Brown, and L. Z. Benet (eds.), Clinical Applications of Mifepristone (RU 486) and Other Antiprogestins, National Academy Press, Washington, DC, 1993, pp. 71-119.
    • (1993) Clinical Applications of Mifepristone (RU 486) and Other Antiprogestins , pp. 71-119
    • Baulieu, E.E.1
  • 40
    • 0019993591 scopus 로고
    • Effet d'un stéroide anti-progestérone chez la femme: Interruption du cycle menstruel et de la grossesse au début
    • W. Herrmann, R. Wyss, A. Riondel, D. Philibert, G. Teutsch, E. Sakiz, and E. E. Baulieu. Effet d'un stéroide anti-progestérone chez la femme: Interruption du cycle menstruel et de la grossesse au début [The effects of an antiprogesterone steroid in women: Interruption of the menstrual cycle and of early pregnancy]. Compt. Rend. 294:933-938 (1982).
    • (1982) Compt. Rend. , vol.294 , pp. 933-938
    • Herrmann, W.1    Wyss, R.2    Riondel, A.3    Philibert, D.4    Teutsch, G.5    Sakiz, E.6    Baulieu, E.E.7
  • 42
    • 0022908051 scopus 로고
    • Termination of early pregnancy by the progesterone antagonist RU 486 (Mifepristone)
    • B. Couzinet, S. N. Le, A. Ulmann, E. E. Baulieu, and G. Schaison. Termination of early pregnancy by the progesterone antagonist RU 486 (Mifepristone). New. Engl. J. Med. 315:1565-1570 (1986).
    • (1986) New. Engl. J. Med. , vol.315 , pp. 1565-1570
    • Couzinet, B.1    Le, S.N.2    Ulmann, A.3    Baulieu, E.E.4    Schaison, G.5
  • 45
    • 0021995017 scopus 로고
    • Progesterone receptor blockage. Effect on uterine contractility and early pregnancy
    • M. Bygdeman and M. L. Swahn. Progesterone receptor blockage. Effect on uterine contractility and early pregnancy. Contraception 32:45-51 (1985).
    • (1985) Contraception , vol.32 , pp. 45-51
    • Bygdeman, M.1    Swahn, M.L.2
  • 46
    • 0027507584 scopus 로고
    • The effect of mifepristone (RU486) on the immunohistochemical distribution of prostaglandin e and its metabolite in decidual and chorionic tissue in early pregnancy
    • L. Cheng, R. W. Kelly, K. J. Thong, R. Hume, and D. T. Baird. The effect of mifepristone (RU486) on the immunohistochemical distribution of prostaglandin E and its metabolite in decidual and chorionic tissue in early pregnancy. J. Clin. Endocrinol. Metab. 77:873-877 (1993).
    • (1993) J. Clin. Endocrinol. Metab. , vol.77 , pp. 873-877
    • Cheng, L.1    Kelly, R.W.2    Thong, K.J.3    Hume, R.4    Baird, D.T.5
  • 47
    • 0027152006 scopus 로고
    • The effects of mifepristone (RU486) on prostaglandin dehydrogenase in decidual and chorionic tissue in early pregnancy
    • L. Cheng, R. W. Kelly, K. J. Thong, R. Hume, and D. T. Baird. The effects of mifepristone (RU486) on prostaglandin dehydrogenase in decidual and chorionic tissue in early pregnancy. Hum. Reprod. 8:705-709 (1993).
    • (1993) Hum. Reprod. , vol.8 , pp. 705-709
    • Cheng, L.1    Kelly, R.W.2    Thong, K.J.3    Hume, R.4    Baird, D.T.5
  • 48
    • 0023475341 scopus 로고
    • Induction of therapeutic abortion in early pregnancy with mifepristone in combination with prostaglandin pessary
    • M. W. Rodger and D. T. Baird. Induction of therapeutic abortion in early pregnancy with mifepristone in combination with prostaglandin pessary. Lancet 2:1415-1418 (1987).
    • (1987) Lancet , vol.2 , pp. 1415-1418
    • Rodger, M.W.1    Baird, D.T.2
  • 49
    • 0024786414 scopus 로고
    • Termination of early pregnancy with RU 486 (mifepristone) in combination with a prostaglandin analogue (sulprostone)
    • M. L. Swahn and M. Bygdeman. Termination of early pregnancy with RU 486 (mifepristone) in combination with a prostaglandin analogue (sulprostone). Acta Obstet. Gynecol. Scand. 68:293-300 (1989).
    • (1989) Acta Obstet. Gynecol. Scand. , vol.68 , pp. 293-300
    • Swahn, M.L.1    Bygdeman, M.2
  • 50
    • 0025818821 scopus 로고
    • Activité contragestive de l'association an RU486 d'une prostaglandine active par voie orale
    • E. Aubeny and E. E. Baulieu. Activité contragestive de l'association an RU486 d'une prostaglandine active par voie orale [Contraceptive activity of RU486 and oral active prostaglandin combination]. Compt. Rend. 312:539-545 (1991).
    • (1991) Compt. Rend. , vol.312 , pp. 539-545
    • Aubeny, E.1    Baulieu, E.E.2
  • 51
    • 0025159060 scopus 로고
    • 1 analog vaginal pessary for the termination of early pregnancy: Complications and patient acceptability
    • 1 analog vaginal pessary for the termination of early pregnancy: Complications and patient acceptability. Am. J. Obstet. Gynecol. 162:414-417 (1990).
    • (1990) Am. J. Obstet. Gynecol. , vol.162 , pp. 414-417
    • Hill, N.C.1    Ferguson, J.2    MacKenzie, I.Z.3
  • 52
    • 0025308974 scopus 로고
    • The efficacy and tolerance of mifepristone and prostaglandin in first trimester termination of pregnancy. UK Multicentre Trial
    • The efficacy and tolerance of mifepristone and prostaglandin in first trimester termination of pregnancy. UK Multicentre Trial. Br. J. Obstet. Gynaecol. 97:480-486 (1990).
    • (1990) Br. J. Obstet. Gynaecol. , vol.97 , pp. 480-486
  • 53
    • 0026004552 scopus 로고
    • Uterine contractility and induction of abortion in early pregnancy by misoprostol and mifepristone
    • J. E. Norman, K. J. Thong, and D. T. Baird. Uterine contractility and induction of abortion in early pregnancy by misoprostol and mifepristone [see comments]. Lancet 338:1233-1236 (1991).
    • (1991) Lancet , vol.338 , pp. 1233-1236
    • Norman, J.E.1    Thong, K.J.2    Baird, D.T.3
  • 55
    • 0025304788 scopus 로고
    • Voluntary interruption of pregnancy with mifepristone (RU 486) and a prostaglandin analogue. A large-scale French experience
    • L. Silvestre, C. Dubois, M. Renault, Y. Rezvani, E. E. Baulieu, and A. Ulmann. Voluntary interruption of pregnancy with mifepristone (RU 486) and a prostaglandin analogue. A large-scale French experience [see comments]. New Engl. J. Med. 322:645-648 (1990).
    • (1990) New Engl. J. Med. , vol.322 , pp. 645-648
    • Silvestre, L.1    Dubois, C.2    Renault, M.3    Rezvani, Y.4    Baulieu, E.E.5    Ulmann, A.6
  • 56
    • 0031022921 scopus 로고    scopus 로고
    • The efficacy and tolerance of mifepristone and prostaglandin in termination of pregnancy of less than 63 days gestation; UK Multicentre Study - Final results
    • The efficacy and tolerance of mifepristone and prostaglandin in termination of pregnancy of less than 63 days gestation; UK Multicentre Study - final results. Contraception 55:1-5 (1997).
    • (1997) Contraception , vol.55 , pp. 1-5
  • 57
    • 0030897554 scopus 로고    scopus 로고
    • Vaginal misoprostol administered at home after mifepristone (RU486) for abortion
    • E. A. Schaff, L. S. Stadalius, S. H. Eisinger, and P. Franks. Vaginal misoprostol administered at home after mifepristone (RU486) for abortion. J. Fam. Practice 44:353-360 (1997).
    • (1997) J. Fam. Practice , vol.44 , pp. 353-360
    • Schaff, E.A.1    Stadalius, L.S.2    Eisinger, S.H.3    Franks, P.4
  • 60
    • 0028040033 scopus 로고
    • Termination of early pregnancy with ZK 98.734; pharmacokinetic behavior and clinical effect
    • M. L. Swahn, L. Kovacs, S. Z. Cekan, A. R. Aedo, and P. Westlund. Termination of early pregnancy with ZK 98.734; pharmacokinetic behavior and clinical effect. Hum. Reprod. 9:57-63 (1994).
    • (1994) Hum. Reprod. , vol.9 , pp. 57-63
    • Swahn, M.L.1    Kovacs, L.2    Cekan, S.Z.3    Aedo, A.R.4    Westlund, P.5
  • 61
    • 0023624268 scopus 로고
    • Synthesis of antiprogestational steroids
    • R. Wiechert and G. Neef. Synthesis of antiprogestational steroids. J. Steroid Biochem. 27:851-858 (1987).
    • (1987) J. Steroid Biochem. , vol.27 , pp. 851-858
    • Wiechert, R.1    Neef, G.2
  • 62
  • 63
    • 0028543657 scopus 로고
    • Expression of the mdrl P-glycoprotein gene: A mechanism of escape from glucocorticoid-induced apoptosis
    • D. J. Gruol and S. Bourgeois. Expression of the mdrl P-glycoprotein gene: A mechanism of escape from glucocorticoid-induced apoptosis. Biochem. Cell Biol. 72:561-571 (1994).
    • (1994) Biochem. Cell Biol. , vol.72 , pp. 561-571
    • Gruol, D.J.1    Bourgeois, S.2
  • 64
    • 0028028123 scopus 로고
    • The antiprogestatin drug RU 486 potentiates doxorubicin cytotoxicity in multidrug resistant cells through inhibition of P-glycoprotein function
    • V. Lecureur, O. Fardel, and A. Guillouzo. The antiprogestatin drug RU 486 potentiates doxorubicin cytotoxicity in multidrug resistant cells through inhibition of P-glycoprotein function. FEBS Lett. 355:187-191 (1994).
    • (1994) FEBS Lett. , vol.355 , pp. 187-191
    • Lecureur, V.1    Fardel, O.2    Guillouzo, A.3
  • 66
    • 0028272514 scopus 로고
    • Clinical efficacy of the antiprogesterone RU486 in the treatment of endometriosis and uterine fibroids
    • L. M. Kettel, A. A. Murphy, A. J. Morales, and S. S. Yen. Clinical efficacy of the antiprogesterone RU486 in the treatment of endometriosis and uterine fibroids. Hum. Reprod. 9 (Suppl. 1):116-120 (1994).
    • (1994) Hum. Reprod. , vol.9 , Issue.1 SUPPL. , pp. 116-120
    • Kettel, L.M.1    Murphy, A.A.2    Morales, A.J.3    Yen, S.S.4
  • 68
    • 0019425414 scopus 로고
    • Uterine leiomyomata: Etiology, symptomatology, and management
    • V. J. Buttram and R. C. Reiter. Uterine leiomyomata: Etiology, symptomatology, and management. Fertil. Steril. 36:433-445 (1981).
    • (1981) Fertil. Steril. , vol.36 , pp. 433-445
    • Buttram, V.J.1    Reiter, R.C.2
  • 70
    • 0027408643 scopus 로고
    • Progesterone receptor expression in meningiomas
    • R. S. Carroll, D. Glowacka, and K. Dashner. Progesterone receptor expression in meningiomas. Cancer Res. 53:1312-1316 (1993).
    • (1993) Cancer Res. , vol.53 , pp. 1312-1316
    • Carroll, R.S.1    Glowacka, D.2    Dashner, K.3
  • 71
    • 0028265544 scopus 로고
    • Antitumor effects of antiprogesterones on human meningioma cells in vitro and in vivo
    • Y. Matsuda, K. Kawamoto, K. Kiya, K. Kurisu, K. Sugiyama, and T. Uozumi. Antitumor effects of antiprogesterones on human meningioma cells in vitro and in vivo. J. Neurosurg. 80:527-534 (1994).
    • (1994) J. Neurosurg. , vol.80 , pp. 527-534
    • Matsuda, Y.1    Kawamoto, K.2    Kiya, K.3    Kurisu, K.4    Sugiyama, K.5    Uozumi, T.6
  • 72
    • 0028301213 scopus 로고
    • Role of antiprogestational therapy for meningiomas
    • S. M. Grunberg. Role of antiprogestational therapy for meningiomas. Hum. Reprod. 9 (Suppl. 1):202-207 (1994).
    • (1994) Hum. Reprod. , vol.9 , Issue.1 SUPPL. , pp. 202-207
    • Grunberg, S.M.1
  • 73
    • 0021941831 scopus 로고
    • RU486, a progestin and glucocorticoid antagonist, inhibits the growth of breast cancer cells via the progesterone receptor
    • S. Bardon, F. Vignon, D. Chalbos, and H. Rochefort. RU486, a progestin and glucocorticoid antagonist, inhibits the growth of breast cancer cells via the progesterone receptor. J. Clin. Endocrinol. Metab. 60:692-697 (1985).
    • (1985) J. Clin. Endocrinol. Metab. , vol.60 , pp. 692-697
    • Bardon, S.1    Vignon, F.2    Chalbos, D.3    Rochefort, H.4
  • 74
    • 0023485819 scopus 로고
    • Comparison of the actions of the antiprogestin mifepristone (RU486), the progestin megestrol acetate, the LHRH analog buserelin, and ovariectomy in treatment of rat mammary tumors
    • G. H. Bakker, H. B. Setyono, M. S. Henkelman, F. H. de Jong, S. W. Lamberts, P. van der Schoot, and J. G. Klijn. Comparison of the actions of the antiprogestin mifepristone (RU486), the progestin megestrol acetate, the LHRH analog buserelin, and ovariectomy in treatment of rat mammary tumors. Cancer Treat. Rev. 71:1021-1027 (1987).
    • (1987) Cancer Treat. Rev. , vol.71 , pp. 1021-1027
    • Bakker, G.H.1    Setyono, H.B.2    Henkelman, M.S.3    De Jong, F.H.4    Lamberts, S.W.5    Van Der Schoot, P.6    Klijn, J.G.7
  • 75
    • 0023755327 scopus 로고
    • Effect of medroxyprogesterone acetate on proliferation and cell cycle kinetics of human mammary carcinoma cells
    • R. L. Sutherland, R. E. Hall, G. Y. Pang, E. A. Musgrove, and C. L. Clarke. Effect of medroxyprogesterone acetate on proliferation and cell cycle kinetics of human mammary carcinoma cells. Cancer Res. 48:5084-5091 (1988).
    • (1988) Cancer Res. , vol.48 , pp. 5084-5091
    • Sutherland, R.L.1    Hall, R.E.2    Pang, G.Y.3    Musgrove, E.A.4    Clarke, C.L.5
  • 76
    • 0024507018 scopus 로고
    • Growth stimulation of T47D human breast cancer cells by the anti-progestin RU486
    • R. T. Bowden, J. R. Hissom, and M. R. Moore. Growth stimulation of T47D human breast cancer cells by the anti-progestin RU486. Endocrinology 124:2642-2644 (1989).
    • (1989) Endocrinology , vol.124 , pp. 2642-2644
    • Bowden, R.T.1    Hissom, J.R.2    Moore, M.R.3
  • 77
    • 0024461465 scopus 로고
    • Endocrine and antitumor effects of combined treatment with an antiprogestin and antiestrogen or luteinizing hormone-releasing hormone agonist in female rats bearing mammary tumors
    • G. H. Bakker, H. B. Setyono, H. Portengen, F. H. De Jong, J. A. Foekens, and J. G. Klijn. Endocrine and antitumor effects of combined treatment with an antiprogestin and antiestrogen or luteinizing hormone-releasing hormone agonist in female rats bearing mammary tumors. Endocrinology 125:1593-1598 (1989).
    • (1989) Endocrinology , vol.125 , pp. 1593-1598
    • Bakker, G.H.1    Setyono, H.B.2    Portengen, H.3    De Jong, F.H.4    Foekens, J.A.5    Klijn, J.G.6
  • 79
    • 0024822416 scopus 로고
    • Antitumor activity of the antiprogestins ZK 98.299 and RU 38.486 in hormone dependent rat and mouse mammary tumors: Mechanistic studies
    • H. Michna, M. R. Schneider, Y. Nishino, and M. F. el Etreby. Antitumor activity of the antiprogestins ZK 98.299 and RU 38.486 in hormone dependent rat and mouse mammary tumors: Mechanistic studies. Breast Cancer Res. Treat. 14:275-288 (1989).
    • (1989) Breast Cancer Res. Treat. , vol.14 , pp. 275-288
    • Michna, H.1    Schneider, M.R.2    Nishino, Y.3    El Etreby, M.F.4
  • 82
    • 0029739075 scopus 로고    scopus 로고
    • Phase II study of the progesterone antagonist mifepristone in patients with untreated metastatic breast carcinoma: A National Cancer Institute of Canada Clinical Trials Group study
    • D. Perrault, E. A. Eisenhauer, K. I. Pritchard, L. Panasci, B. Norris, T. Vandenberg, and B. Fisher. Phase II study of the progesterone antagonist mifepristone in patients with untreated metastatic breast carcinoma: A National Cancer Institute of Canada Clinical Trials Group study. J. Clin. Oncol. 14:2709-2712 (1996).
    • (1996) J. Clin. Oncol. , vol.14 , pp. 2709-2712
    • Perrault, D.1    Eisenhauer, E.A.2    Pritchard, K.I.3    Panasci, L.4    Norris, B.5    Vandenberg, T.6    Fisher, B.7
  • 83
    • 0029882238 scopus 로고    scopus 로고
    • Mifepristone: Antineoplastic studies
    • O. Sartor and W. D. Figg. Mifepristone: antineoplastic studies. Clin. Obstet. Gynecol. 39:498-505 (1996).
    • (1996) Clin. Obstet. Gynecol. , vol.39 , pp. 498-505
    • Sartor, O.1    Figg, W.D.2
  • 84
    • 0028910730 scopus 로고
    • Growth inhibition of androgen-insensitive human prostate carcinoma cells by a 19-norsteroid derivative agent, mifepristone
    • M. F. Lin, M. H. Kawachi, M. R. Stallcup, S. M. Grunberg, and F. F. Lin. Growth inhibition of androgen-insensitive human prostate carcinoma cells by a 19-norsteroid derivative agent, mifepristone. Prostate 26:194-204 (1995).
    • (1995) Prostate , vol.26 , pp. 194-204
    • Lin, M.F.1    Kawachi, M.H.2    Stallcup, M.R.3    Grunberg, S.M.4    Lin, F.F.5
  • 85
    • 0026658614 scopus 로고
    • Inhibition of ovulation by low-dose mifepristone (RU 486)
    • W. L. Ledger, V. M. Sweeting, H. Hillier, and D. T. Baird. Inhibition of ovulation by low-dose mifepristone (RU 486). Hum. Reprod. 7:945-950 (1992).
    • (1992) Hum. Reprod. , vol.7 , pp. 945-950
    • Ledger, W.L.1    Sweeting, V.M.2    Hillier, H.3    Baird, D.T.4
  • 86
    • 0027481262 scopus 로고
    • Effects of continuous treatment with low dose mifepristone throughout one menstrual cycle
    • H. B. Croxatto, A. M. Salvatierra, H. D. Croxatto, and B. Fuentealba. Effects of continuous treatment with low dose mifepristone throughout one menstrual cycle. Hum. Reprod. 8:201-207 (1993).
    • (1993) Hum. Reprod. , vol.8 , pp. 201-207
    • Croxatto, H.B.1    Salvatierra, A.M.2    Croxatto, H.D.3    Fuentealba, B.4
  • 89
    • 0027243195 scopus 로고
    • Early luteal phase treatment with mifepristone (RU 486) for fertility regulation
    • K. Gemzell-Danielsson, M. L. Swahn, P. Svalander, and M. Bygdeman. Early luteal phase treatment with mifepristone (RU 486) for fertility regulation. Hum. Reprod. 8:870-873 (1993).
    • (1993) Hum. Reprod. , vol.8 , pp. 870-873
    • Gemzell-Danielsson, K.1    Swahn, M.L.2    Svalander, P.3    Bygdeman, M.4
  • 90
    • 0030954657 scopus 로고    scopus 로고
    • The effect of a single dose of mifepristone (RU486) on the fine structure of the human endometrium during the early luteal phase
    • P. Dockery, R. M. Ismail, T. C. Li, M. A. Warren, and I. D. Cooke. The effect of a single dose of mifepristone (RU486) on the fine structure of the human endometrium during the early luteal phase. Hum. Reprod. 12:1778-1784 (1997).
    • (1997) Hum. Reprod. , vol.12 , pp. 1778-1784
    • Dockery, P.1    Ismail, R.M.2    Li, T.C.3    Warren, M.A.4    Cooke, I.D.5
  • 91
    • 0343488606 scopus 로고    scopus 로고
    • Effects of two antiprogestins (mifepristone and onapristone) on endometrial factors of potential importance for implantation
    • S. T. Cameron, H. O. Critchley, C. H. Buckley, R. W. Kelly, and D. T. Baird. Effects of two antiprogestins (mifepristone and onapristone) on endometrial factors of potential importance for implantation. Fertil. Steril. 67:1046-1053 (1997).
    • (1997) Fertil. Steril. , vol.67 , pp. 1046-1053
    • Cameron, S.T.1    Critchley, H.O.2    Buckley, C.H.3    Kelly, R.W.4    Baird, D.T.5
  • 93
    • 0025674140 scopus 로고
    • Late luteal administration of the antiprogesterone RU486 in normal women: Effects on the menstrual cycle events and fertility control in a long-term study
    • B. Couzinet, S. N. Le, L. Silvestre, and G. Schaison. Late luteal administration of the antiprogesterone RU486 in normal women: Effects on the menstrual cycle events and fertility control in a long-term study. Fertil. Steril. 54:1039-1044 (1990).
    • (1990) Fertil. Steril. , vol.54 , pp. 1039-1044
    • Couzinet, B.1    Le, S.N.2    Silvestre, L.3    Schaison, G.4
  • 94
    • 0026761586 scopus 로고
    • Mifepristone (RU 486) compared with high-dose estrogen and progestogen for emergency postcoital contraception
    • A. Glasier, K. J. Thong, M. Dewar, M. Mackie, and D. T. Baird. Mifepristone (RU 486) compared with high-dose estrogen and progestogen for emergency postcoital contraception [see comments]. New Engl. J. Med. 327:1041-1044 (1992).
    • (1992) New Engl. J. Med. , vol.327 , pp. 1041-1044
    • Glasier, A.1    Thong, K.J.2    Dewar, M.3    Mackie, M.4    Baird, D.T.5
  • 95
    • 0026641672 scopus 로고
    • Comparison of Yuzpe regimen, danazol, and mifepristone (RU486) in oral postcoital contraception
    • A. M. Webb, J. Russell, and M. Elstein. Comparison of Yuzpe regimen, danazol, and mifepristone (RU486) in oral postcoital contraception. Br. Med. J. 305:927-931 (1992).
    • (1992) Br. Med. J. , vol.305 , pp. 927-931
    • Webb, A.M.1    Russell, J.2    Elstein, M.3
  • 96
  • 100
    • 0024470651 scopus 로고
    • Contragestion and other clinical applications of RU 486, an antiprogesterone at the receptor
    • E. E. Baulieu. Contragestion and other clinical applications of RU 486, an antiprogesterone at the receptor. Science 245:1351-1357 (1989).
    • (1989) Science , vol.245 , pp. 1351-1357
    • Baulieu, E.E.1
  • 102
    • 0025196163 scopus 로고
    • Antiprogesterone steroid RU486. Pharmacokinetics and receptor binding in humans
    • O. Heikinheimo. Antiprogesterone steroid RU486. Pharmacokinetics and receptor binding in humans. Acta Obstet. Gynecol. Scand. 69:357-358 (1990).
    • (1990) Acta Obstet. Gynecol. Scand. , vol.69 , pp. 357-358
    • Heikinheimo, O.1
  • 103
    • 0026148814 scopus 로고
    • Automated direct assay system for RU38486, an antiprogesterone-antiglucocorticoid agent, and its metabolites using high performance liquid chromatography
    • K. Nagoshi, N. Hayashi, and K. Sekiba. Automated direct assay system for RU38486, an antiprogesterone-antiglucocorticoid agent, and its metabolites using high performance liquid chromatography. Acta Med. Okayama 45:81-87 (1991).
    • (1991) Acta Med. Okayama , vol.45 , pp. 81-87
    • Nagoshi, K.1    Hayashi, N.2    Sekiba, K.3
  • 104
    • 0027296437 scopus 로고
    • Pharmacokinetic study of RU 486 and its metabolites after oral administration of single doses to pregnant and non-pregnant women
    • Y. E. Shi, Z. H. Ye, C. H. He, G. Q. Zhang, J. Q. Xu, L. P. Van, and K. Fotherby. Pharmacokinetic study of RU 486 and its metabolites after oral administration of single doses to pregnant and non-pregnant women. Contraception 48:133-149 (1993).
    • (1993) Contraception , vol.48 , pp. 133-149
    • Shi, Y.E.1    Ye, Z.H.2    He, C.H.3    Zhang, G.Q.4    Xu, J.Q.5    Van, L.P.6    Fotherby, K.7
  • 105
    • 0024494292 scopus 로고
    • Pharmacokinetics of the antiprogesterone RU 486 in women during multiple dose administration
    • O. Heikinheimo. Pharmacokinetics of the antiprogesterone RU 486 in women during multiple dose administration. J. Steroid Biochem. 32:21-25 (1989).
    • (1989) J. Steroid Biochem. , vol.32 , pp. 21-25
    • Heikinheimo, O.1
  • 106
    • 0031016232 scopus 로고    scopus 로고
    • Alterations in the pituitary-thyroid and pituitary-adrenal axes - Consequences of long-term mifepristone treatment
    • O. Heikinheimo, S. Ranta, S. Grunberg, P. Lähteenmäki, and I. M. Spitz. Alterations in the pituitary-thyroid and pituitary-adrenal axes - consequences of long-term mifepristone treatment. Metabolism 46:292-296 (1997).
    • (1997) Metabolism , vol.46 , pp. 292-296
    • Heikinheimo, O.1    Ranta, S.2    Grunberg, S.3    Lähteenmäki, P.4    Spitz, I.M.5
  • 107
    • 0025089162 scopus 로고
    • Pharmacokinetics of the antiprogesterone RU 486: No correlation to clinical performance of RU 486
    • O. Heikinheimo, O. Ylikorkala, U. Turpeinen, and P. Lähteenmäki. Pharmacokinetics of the antiprogesterone RU 486: No correlation to clinical performance of RU 486. Acta Endocrinol. 123:298-304 (1990).
    • (1990) Acta Endocrinol. , vol.123 , pp. 298-304
    • Heikinheimo, O.1    Ylikorkala, O.2    Turpeinen, U.3    Lähteenmäki, P.4
  • 108
    • 0037801621 scopus 로고
    • Antiprogestins: Perspectives from a Global Research Program
    • M. S. Donaldson, L. Dorflinger, S. S. Brown, and L. Z. Benet (eds.), National Academy Press, Washington, DC
    • P. F. A. Van Look and H. Von Hertzen. Antiprogestins: Perspectives from a Global Research Program. In M. S. Donaldson, L. Dorflinger, S. S. Brown, and L. Z. Benet (eds.), Clinical Applications of Mifepristone (RU 486) and Other Antiprogestins, National Academy Press, Washington, DC, 1993, pp. 253-277.
    • (1993) Clinical Applications of Mifepristone (RU 486) and Other Antiprogestins , pp. 253-277
    • Van Look, P.F.A.1    Von Hertzen, H.2
  • 109
    • 0030582402 scopus 로고    scopus 로고
    • Identification of CYP3A4 as the principal enzyme catalyzing mifepristone (RU 486) oxidation in human liver microsomes
    • G. R. Jang, S. A. Wrighton, and L. Z. Benet. Identification of CYP3A4 as the principal enzyme catalyzing mifepristone (RU 486) oxidation in human liver microsomes. Biochem. Pharmacol. 52:753-761 (1996).
    • (1996) Biochem. Pharmacol. , vol.52 , pp. 753-761
    • Jang, G.R.1    Wrighton, S.A.2    Benet, L.Z.3
  • 111
    • 0030846064 scopus 로고    scopus 로고
    • Cytochrome P450 3A4 mediated N-demethylation of the antiprogestins Iilopristone and onapristone
    • G. R. Jang and L. Z. Benet. Cytochrome P450 3A4 mediated N-demethylation of the antiprogestins Iilopristone and onapristone. Drug Metab. Dispos. 25:1119-1122 (1997).
    • (1997) Drug Metab. Dispos. , vol.25 , pp. 1119-1122
    • Jang, G.R.1    Benet, L.Z.2
  • 112
    • 0031931151 scopus 로고    scopus 로고
    • Antiprogestin-mediated inactivation of cytochrome P450 3A4
    • G. R. Jang and L. Z. Benet. Antiprogestin-mediated inactivation of cytochrome P450 3A4. Pharmacology, 56:150-157 (1998).
    • (1998) Pharmacology , vol.56 , pp. 150-157
    • Jang, G.R.1    Benet, L.Z.2
  • 113
    • 0028918996 scopus 로고
    • Comparative analysis of cytochrome P4503A induction in primary cultures of rat, rabbit, and human hepatocytes
    • T. A. Kocarek, E. G. Schuetz, S. C. Strom, R. A. Fisher, and P. S. Guzelian. Comparative analysis of cytochrome P4503A induction in primary cultures of rat, rabbit, and human hepatocytes. Drug Metab. Dispos. 23:415-421 (1995).
    • (1995) Drug Metab. Dispos. , vol.23 , pp. 415-421
    • Kocarek, T.A.1    Schuetz, E.G.2    Strom, S.C.3    Fisher, R.A.4    Guzelian, P.S.5
  • 114
    • 0002769936 scopus 로고    scopus 로고
    • Pharmacokinetics: The dynamics of drug absorption, distribution, and elimination
    • J. G. Hardman, L. E. Limbird, P. B. Molinoff, R. W. Ruddon, and A. G. Goodman (eds.), McGraw-Hill, New York, chap. 1
    • L. Z. Benet, D. L. Kroetz, and L. B. Sheiner. Pharmacokinetics: The dynamics of drug absorption, distribution, and elimination. In J. G. Hardman, L. E. Limbird, P. B. Molinoff, R. W. Ruddon, and A. G. Goodman (eds.), Goodman and Gilman's The Pharmacological Basis of Therapeutics, McGraw-Hill, New York, 1996, chap. 1, pp. 3-27.
    • (1996) Goodman and Gilman's the Pharmacological Basis of Therapeutics , pp. 3-27
    • Benet, L.Z.1    Kroetz, D.L.2    Sheiner, L.B.3
  • 115
    • 0022998708 scopus 로고
    • Characterization of rat and human liver microsomal cytochrome P-450 forms involved in nifedipine oxidation, a prototype for genetic polymorphism in oxidative drug metabolism
    • F. P. Guengerich, M. V. Martin, P. H. Beaune, P. Kremers, T. Wolff, and D. J. Waxman. Characterization of rat and human liver microsomal cytochrome P-450 forms involved in nifedipine oxidation, a prototype for genetic polymorphism in oxidative drug metabolism. J. Biol. Chem. 261:5051-5060 (1986).
    • (1986) J. Biol. Chem. , vol.261 , pp. 5051-5060
    • Guengerich, F.P.1    Martin, M.V.2    Beaune, P.H.3    Kremers, P.4    Wolff, T.5    Waxman, D.J.6
  • 116
    • 0023921505 scopus 로고
    • Cyclosporine metabolism in human liver: Identification of a cytochrome P-450III gene family as the major cyclosporine-metabolizing enzyme explains interactions of cyclosporine with other drugs
    • T. Kronbach, V. Fischer, and U. A. Meyer. Cyclosporine metabolism in human liver: Identification of a cytochrome P-450III gene family as the major cyclosporine-metabolizing enzyme explains interactions of cyclosporine with other drugs. Clin. Pharmacol. Ther. 43:630-635 (1988).
    • (1988) Clin. Pharmacol. Ther. , vol.43 , pp. 630-635
    • Kronbach, T.1    Fischer, V.2    Meyer, U.A.3
  • 117
    • 0026662551 scopus 로고
    • Cytochrome P-450 3A enzymes are responsible for biotransformation of FK506 and rapamycin in man and rat
    • M. Sattler, F. P. Guengerich, C. H. Yun, U. Christians, and K. F. Sewing. Cytochrome P-450 3A enzymes are responsible for biotransformation of FK506 and rapamycin in man and rat. Drug Metab. Dispos. 20:753-761 (1992).
    • (1992) Drug Metab. Dispos. , vol.20 , pp. 753-761
    • Sattler, M.1    Guengerich, F.P.2    Yun, C.H.3    Christians, U.4    Sewing, K.F.5
  • 118
    • 0024373348 scopus 로고
    • Oxidation of midazolam and triazolam by human liver cytochrome P450IIIA4
    • T. Kronbach, D. Mathys, M. Umeno, F. J. Gonzalez, and U. A. Meyer. Oxidation of midazolam and triazolam by human liver cytochrome P450IIIA4. Mol. Pharmacol. 36:89-96 (1989).
    • (1989) Mol. Pharmacol. , vol.36 , pp. 89-96
    • Kronbach, T.1    Mathys, D.2    Umeno, M.3    Gonzalez, F.J.4    Meyer, U.A.5
  • 119
    • 0025601454 scopus 로고
    • Lidocaine metabolism by human cytochrome P-450s purified from hepatic microsomes: Comparison of those with rat hepatic cytochrome P-450s
    • S. Imaoka, K. Enomoto, Y. Oda, A. Asada, M. Fujimori, T. Shimada, S. Fujita, F. P. Guengerich, and Y. Funae. Lidocaine metabolism by human cytochrome P-450s purified from hepatic microsomes: comparison of those with rat hepatic cytochrome P-450s. J. Pharmacol. Exp. Ther. 255:1385-1391 (1990).
    • (1990) J. Pharmacol. Exp. Ther. , vol.255 , pp. 1385-1391
    • Imaoka, S.1    Enomoto, K.2    Oda, Y.3    Asada, A.4    Fujimori, M.5    Shimada, T.6    Fujita, S.7    Guengerich, F.P.8    Funae, Y.9
  • 120
    • 0027523641 scopus 로고
    • Amiodarone N-deethylation in human liver microsomes: Involvement of cytochrome P450 3A enzymes (first report)
    • J. M. Trivier, C. Libersa, C. Belloc, and M. Lhermitte. Amiodarone N-deethylation in human liver microsomes: Involvement of cytochrome P450 3A enzymes (first report). Life Sci. 52:PL91-96 (1993).
    • (1993) Life Sci. , vol.52
    • Trivier, J.M.1    Libersa, C.2    Belloc, C.3    Lhermitte, M.4
  • 121
    • 0027379673 scopus 로고
    • Evidence for CYP3A-mediated N-deethylation of amiodarone in human liver microsomal fractions
    • G. Fabre, B. Julian, A. B. Saint, H. Joyeux, and Y. Berger. Evidence for CYP3A-mediated N-deethylation of amiodarone in human liver microsomal fractions. Drug Metab. Dispos. 21:978-985 (1993).
    • (1993) Drug Metab. Dispos. , vol.21 , pp. 978-985
    • Fabre, G.1    Julian, B.2    Saint, A.B.3    Joyeux, H.4    Berger, Y.5
  • 122
    • 0022467917 scopus 로고
    • Oxidation of quinidine by human liver cytochrome P-450
    • F. P. Guengerich, E. D. Muller, and I. A. Blair. Oxidation of quinidine by human liver cytochrome P-450. Mol. Pharmacol. 30:287-295 (1986).
    • (1986) Mol. Pharmacol. , vol.30 , pp. 287-295
    • Guengerich, F.P.1    Muller, E.D.2    Blair, I.A.3
  • 123
    • 0027957132 scopus 로고
    • Metabolism of taxol by human hepatic microsomes and liver slices: Participation of cytochrome P450 3A4 and an unknown P450 enzyme
    • J. W. Harris, A. Rahman, B. R. Kim, F. P. Guengerich, and J. M. Collins. Metabolism of taxol by human hepatic microsomes and liver slices: Participation of cytochrome P450 3A4 and an unknown P450 enzyme. Cancer Res. 54:4026-4035 (1994).
    • (1994) Cancer Res. , vol.54 , pp. 4026-4035
    • Harris, J.W.1    Rahman, A.2    Kim, B.R.3    Guengerich, F.P.4    Collins, J.M.5
  • 125
    • 0027443019 scopus 로고
    • Involvement of human liver cytochrome P450 3A in vinblastine metabolism: Drug interactions
    • P. X. Zhou, E. Seree, X. J. Zhou, M. Placidi, P. Maurel, Y. Barra, and R. Rahmani. Involvement of human liver cytochrome P450 3A in vinblastine metabolism: Drug interactions. Cancer Res. 53:5121-5126 (1993).
    • (1993) Cancer Res. , vol.53 , pp. 5121-5126
    • Zhou, P.X.1    Seree, E.2    Zhou, X.J.3    Placidi, M.4    Maurel, P.5    Barra, Y.6    Rahmani, R.7
  • 126
    • 0027415546 scopus 로고
    • Human liver microsomal cytochrome P450 3A isozymes mediated vindesine biotransformation. Metabolic drug interactions
    • X. J. Zhou, P. X. Zhou, T. Gauthier, M. Placidi, P. Maurel, and R. Rahmani. Human liver microsomal cytochrome P450 3A isozymes mediated vindesine biotransformation. Metabolic drug interactions. Biochem. Pharmacol. 45:853-861 (1993).
    • (1993) Biochem. Pharmacol. , vol.45 , pp. 853-861
    • Zhou, X.J.1    Zhou, P.X.2    Gauthier, T.3    Placidi, M.4    Maurel, P.5    Rahmani, R.6
  • 127
    • 0030428256 scopus 로고    scopus 로고
    • Cytochrome P4503A (CYP3A) metabolism: Prediction of in vivo activity in humans
    • G. R. Wilkinson. Cytochrome P4503A (CYP3A) metabolism: Prediction of in vivo activity in humans. J. Pharmacokin. Biopharm. 24:475-490 (1996).
    • (1996) J. Pharmacokin. Biopharm. , vol.24 , pp. 475-490
    • Wilkinson, G.R.1
  • 128
    • 0021361026 scopus 로고
    • Induction of cytochrome P-450 by glucocorticoids in rat liver. II. Evidence that glucocorticoids regulate induction of cytochrome P-450 by a nonclassical receptor mechanism
    • E. G. Schuetz and P. S. Guzelian. Induction of cytochrome P-450 by glucocorticoids in rat liver. II. Evidence that glucocorticoids regulate induction of cytochrome P-450 by a nonclassical receptor mechanism. J. Biol. Chem. 259:2007-2012 (1984).
    • (1984) J. Biol. Chem. , vol.259 , pp. 2007-2012
    • Schuetz, E.G.1    Guzelian, P.S.2
  • 129
    • 0028789188 scopus 로고
    • A novel cis-acting element in a liver cytochrome P450 3A gene confers synergistic induction by glucocorticoids plus antiglucocorticoids
    • L. C. Quattrochi, A. S. Mills, J. L. Barwick, C. B. Yockey, and P. S. Guzelian. A novel cis-acting element in a liver cytochrome P450 3A gene confers synergistic induction by glucocorticoids plus antiglucocorticoids. J. Biol. Chem. 270:28917-28923 (1995).
    • (1995) J. Biol. Chem. , vol.270 , pp. 28917-28923
    • Quattrochi, L.C.1    Mills, A.S.2    Barwick, J.L.3    Yockey, C.B.4    Guzelian, P.S.5
  • 130
    • 0030059885 scopus 로고    scopus 로고
    • Identification of a novel dexamethasone responsive enhancer in the human CYP3A5 gene and its activation in human and rat liver cells
    • J. D. Schuetz, E. G. Schuetz, J. V. Thottassery, P. S. Guzelian, S. Strom, and D. Sun. Identification of a novel dexamethasone responsive enhancer in the human CYP3A5 gene and its activation in human and rat liver cells. Mol. Pharmacol. 49:63-72 (1996).
    • (1996) Mol. Pharmacol. , vol.49 , pp. 63-72
    • Schuetz, J.D.1    Schuetz, E.G.2    Thottassery, J.V.3    Guzelian, P.S.4    Strom, S.5    Sun, D.6
  • 131
    • 0030002504 scopus 로고    scopus 로고
    • Intestinal drug metabolism and antitransport processes: A potential paradigm shift in oral drug delivery
    • L. Z. Benet, C.-Y. Wu, M. F. Hebert, and V. J. Wacher. Intestinal drug metabolism and antitransport processes: A potential paradigm shift in oral drug delivery. J. Controlled Release 39:139-143 (1996).
    • (1996) J. Controlled Release , vol.39 , pp. 139-143
    • Benet, L.Z.1    Wu, C.-Y.2    Hebert, M.F.3    Wacher, V.J.4
  • 134
    • 0029028792 scopus 로고
    • Overlapping substrate specificities and tissue distribution of cytochrome P450 3A and P-glycoprotein: Implications for drug delivery and activity in cancer chemotherapy
    • V. J. Wacher, C. Y. Wu, and L. Z. Benet. Overlapping substrate specificities and tissue distribution of cytochrome P450 3A and P-glycoprotein: Implications for drug delivery and activity in cancer chemotherapy. Mol. Carcinogen. 13:129-134 (1995).
    • (1995) Mol. Carcinogen. , vol.13 , pp. 129-134
    • Wacher, V.J.1    Wu, C.Y.2    Benet, L.Z.3


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