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Volumn 55, Issue 5, 2011, Pages 1975-1981

Preclinical characterization of naturally occurring polyketide cyclophilin inhibitors from the sanglifehrin family

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOPHILIN INHIBITOR; CYCLOSPORIN A; ISOMERASE; SANGLIFEHRIN A; SANGLIFEHRIN B; SANGLIFEHRIN C; SANGLIFEHRIN D; UNCLASSIFIED DRUG;

EID: 79955536124     PISSN: 00664804     EISSN: 10986596     Source Type: Journal    
DOI: 10.1128/AAC.01627-10     Document Type: Article
Times cited : (47)

References (52)
  • 1
    • 0035869011 scopus 로고    scopus 로고
    • Cyclophilin A regulates HIV-1 infectivity, as demonstrated by gene targeting in human T cells
    • DOI 10.1093/emboj/20.6.1300
    • Braaten, D., and J. Luban. 2001. Cyclophilin A regulates HIV-1 infectivity, as demonstrated by gene targeting in human T cells. EMBO J. 20:1300-1309. (Pubitemid 32233970)
    • (2001) EMBO Journal , vol.20 , Issue.6 , pp. 1300-1309
    • Braaten, D.1    Luban, J.2
  • 2
    • 67650550814 scopus 로고    scopus 로고
    • The isomerase active site of cyclophilin A is critical for hepatitis C virus replication
    • Chatterji, U., et al. 2009. The isomerase active site of cyclophilin A is critical for hepatitis C virus replication. J. Biol. Chem. 284:16998-17005.
    • (2009) J. Biol. Chem. , vol.284 , pp. 16998-17005
    • Chatterji, U.1
  • 3
    • 28844479566 scopus 로고    scopus 로고
    • Naturally occurring capsid substitutions render HIV-1 cyclophilin A independent in human cells and TRIM-cyclophilin-resistant in owl monkey cells
    • Chatterji, U., et al. 2005. Naturally occurring capsid substitutions render HIV-1 cyclophilin A independent in human cells and TRIM-cyclophilin- resistant in owl monkey cells. J. Biol. Chem. 280:40293-40300.
    • (2005) J. Biol. Chem. , vol.280 , pp. 40293-40300
    • Chatterji, U.1
  • 4
    • 77951046665 scopus 로고    scopus 로고
    • HCV resistance to cyclosporin A does not correlate with a resistance of the NS5A-cyclophilin A interaction to cyclophilin inhibitors
    • Chatterji, U., et al. 2010. HCV resistance to cyclosporin A does not correlate with a resistance of the NS5A-cyclophilin A interaction to cyclophilin inhibitors. J. Hepatol. 53:50-56.
    • (2010) J. Hepatol. , vol.53 , pp. 50-56
    • Chatterji, U.1
  • 5
    • 72949100768 scopus 로고    scopus 로고
    • Cyclosporine A inhibits hepatitis C virus nonstructural protein 2 through cyclophilin A
    • Ciesek, S., et al. 2009. Cyclosporine A inhibits hepatitis C virus nonstructural protein 2 through cyclophilin A. Hepatology 50:1638-1645.
    • (2009) Hepatology , vol.50 , pp. 1638-1645
    • Ciesek, S.1
  • 6
    • 62949181285 scopus 로고    scopus 로고
    • Debio 025, a cyclophilin binding molecule, is highly efficient in clearing hepatitis C virus (HCV) replicon-containing cells when used alone or in combination with specifically targeted antiviral therapy for HCV (STAT-C) inhibitors
    • Coelmont, L., et al. 2009. Debio 025, a cyclophilin binding molecule, is highly efficient in clearing hepatitis C virus (HCV) replicon-containing cells when used alone or in combination with specifically targeted antiviral therapy for HCV (STAT-C) inhibitors. Antimicrob. Agents Chemother. 53:967-976.
    • (2009) Antimicrob. Agents Chemother. , vol.53 , pp. 967-976
    • Coelmont, L.1
  • 7
    • 0034283251 scopus 로고    scopus 로고
    • Isolation, characterization and targeted disruption of mouse Ppia: Cyclophilin A is not essential for mammalian cell viability
    • Colgan, J., M. Asmal, and J. Luban. 2000. Isolation, characterization and targeted disruption of mouse Ppia: cyclophilin A is not essential for mammalian cell viability. Genomics 68:167-178.
    • (2000) Genomics , vol.68 , pp. 167-178
    • Colgan, J.1    Asmal, M.2    Luban, J.3
  • 8
    • 65549151252 scopus 로고    scopus 로고
    • An evaluation of the cyclophilin inhibitor Debio 025 and its potential as a treatment for chronic hepatitis C
    • Crabbé, R., et al. 2009. An evaluation of the cyclophilin inhibitor Debio 025 and its potential as a treatment for chronic hepatitis C. Expert Opin. Investig. Drugs 18:211-220.
    • (2009) Expert Opin. Investig. Drugs , vol.18 , pp. 211-220
    • Crabbé, R.1
  • 9
    • 78149425102 scopus 로고    scopus 로고
    • Antiviral therapy for hepatitis C virus: Beyond the standard of care
    • Basel
    • Delang, L., L. Coelmont, and J. Neyts. 2010. Antiviral therapy for hepatitis C virus: beyond the standard of care. Viruses (Basel) 2:826-866.
    • (2010) Viruses , vol.2 , pp. 826-866
    • Delang, L.1    Coelmont, L.2    Neyts, J.3
  • 10
    • 79955529899 scopus 로고    scopus 로고
    • Reference deleted
    • Reference deleted.
  • 11
    • 79955526469 scopus 로고    scopus 로고
    • Reference deleted
    • Reference deleted.
  • 12
    • 0030692139 scopus 로고    scopus 로고
    • All cyclophilins and FK506 binding proteins are, individually and collectively, dispensable for viability in Saccharomyces cerevisiae
    • Dolinski, K., S. Muir, M. Cardenas, and J. Heitman. 1997. All cyclophilins and FK506 binding proteins are, individually and collectively, dispensable for viability in Saccharomyces cerevisiae. Proc. Natl. Acad. Sci. U. S. A. 94:13093-13098.
    • (1997) Proc. Natl. Acad. Sci. U. S. A. , vol.94 , pp. 13093-13098
    • Dolinski, K.1    Muir, S.2    Cardenas, M.3    Heitman, J.4
  • 13
    • 0032971830 scopus 로고    scopus 로고
    • Sanglifehrins A, B, C and D, novel cyclophilin-binding compounds isolated from Streptomyces sp. A92-308110. II. Structure elucidation, stereochemistry and physico-chemical properties
    • Tokyo
    • Fehr, T., J. Kallen, L. Oberer, J. J. Sanglier, and W. Schilling. 1999. Sanglifehrins A, B, C and D, novel cyclophilin-binding compounds isolated from Streptomyces sp. A92-308110. II. Structure elucidation, stereochemistry and physico-chemical properties. J. Antibiot. (Tokyo) 52:474-479.
    • (1999) J. Antibiot. , vol.52 , pp. 474-479
    • Fehr, T.1    Kallen, J.2    Oberer, L.3    Sanglier, J.J.4    Schilling, W.5
  • 14
    • 78149361253 scopus 로고    scopus 로고
    • Cyclosporine inhibits a direct interaction between cyclophilins and hepatitis C NS5A
    • Fernandes, F., I. U. Ansari, and R. Striker. 2010. Cyclosporine inhibits a direct interaction between cyclophilins and hepatitis C NS5A. PLoS One 5:e9815.
    • (2010) PLoS One , vol.5
    • Fernandes, F.1    Ansari, I.U.2    Striker, R.3
  • 15
    • 66149129922 scopus 로고    scopus 로고
    • The cyclophilin inhibitor Debio 025 combined with PEG IFNalpha2a significantly reduces viral load in treatment-naive hepatitis C patients
    • Flisiak, R., et al. 2009. The cyclophilin inhibitor Debio 025 combined with PEG IFNalpha2a significantly reduces viral load in treatment-naive hepatitis C patients. Hepatology 49:1460-1468.
    • (2009) Hepatology , vol.49 , pp. 1460-1468
    • Flisiak, R.1
  • 17
    • 73949094080 scopus 로고    scopus 로고
    • Multiple cyclophilins involved in different cellular pathways mediate HCV replication
    • Gaither, L. A., et al. 2010. Multiple cyclophilins involved in different cellular pathways mediate HCV replication. Virology 397:43-55.
    • (2010) Virology , vol.397 , pp. 43-55
    • Gaither, L.A.1
  • 18
    • 70349605387 scopus 로고    scopus 로고
    • Identification of cellular and viral factors related to anti-hepatitis C virus activity of cyclophilin inhibitor
    • Goto, K., K. Watashi, D. Inoue, M. Hijikata, and K. Shimotohno. 2009. Identification of cellular and viral factors related to anti-hepatitis C virus activity of cyclophilin inhibitor. Cancer Sci. 100:1943-1950.
    • (2009) Cancer Sci. , vol.100 , pp. 1943-1950
    • Goto, K.1    Watashi, K.2    Inoue, D.3    Hijikata, M.4    Shimotohno, K.5
  • 19
    • 67649412015 scopus 로고    scopus 로고
    • Hepatitis C virus NS5A protein is a substrate for the peptidyl-prolyl cis/trans isomerase activity of cyclophilins A and B
    • Hanoulle, X., et al. 2009. Hepatitis C virus NS5A protein is a substrate for the peptidyl-prolyl cis/trans isomerase activity of cyclophilins A and B. J. Biol. Chem. 284:13589-13601.
    • (2009) J. Biol. Chem. , vol.284 , pp. 13589-13601
    • Hanoulle, X.1
  • 20
    • 0028217756 scopus 로고
    • Cloning and characterization of ppiB, a Bacillus subtilis gene which encodes a cyclosporin A-sensitive peptidyl-prolyl cis-trans isomerase
    • Herrler, M., H. Bang, and M. A. Marahiel. 1994. Cloning and characterization of ppiB, a Bacillus subtilis gene which encodes a cyclosporin A-sensitive peptidyl-prolyl cis-trans isomerase. Mol. Microbiol. 11:1073-1083.
    • (1994) Mol. Microbiol. , vol.11 , pp. 1073-1083
    • Herrler, M.1    Bang, H.2    Marahiel, M.A.3
  • 21
    • 75749110945 scopus 로고    scopus 로고
    • SCY-635, a novel nonimmunosuppressive analog of cyclosporine that exhibits potent inhibition of hepatitis C virus RNA replication in vitro
    • Hopkins, S., et al. 2010. SCY-635, a novel nonimmunosuppressive analog of cyclosporine that exhibits potent inhibition of hepatitis C virus RNA replication in vitro. Antimicrob. Agents Chemother. 54:660-672.
    • (2010) Antimicrob. Agents Chemother. , vol.54 , pp. 660-672
    • Hopkins, S.1
  • 22
    • 3543067010 scopus 로고    scopus 로고
    • Purification and characterization of hepatitis C virus non-structural protein 5A expressed in Escherichia coli
    • Huang, L., et al. 2004. Purification and characterization of hepatitis C virus non-structural protein 5A expressed in Escherichia coli. Protein Expr. Purif. 37:144-153.
    • (2004) Protein Expr. Purif. , vol.37 , pp. 144-153
    • Huang, L.1
  • 24
    • 33646194456 scopus 로고    scopus 로고
    • Diverse effects of cyclosporine on hepatitis C virus strain replication
    • Ishii, N., et al. 2006. Diverse effects of cyclosporine on hepatitis C virus strain replication. J. Virol. 80:4510-4520.
    • (2006) J. Virol. , vol.80 , pp. 4510-4520
    • Ishii, N.1
  • 26
    • 20444479819 scopus 로고    scopus 로고
    • Structure of human cyclophilin A in complex with the novel immunosuppressant sanglifehrin A at 1.6 A resolution
    • Kallen, J., R. Sedrani, G. Zenke, and J. Wagner. 2005. Structure of human cyclophilin A in complex with the novel immunosuppressant sanglifehrin A at 1.6 A resolution. J. Biol. Chem. 280:21965-21971.
    • (2005) J. Biol. Chem. , vol.280 , pp. 21965-21971
    • Kallen, J.1    Sedrani, R.2    Zenke, G.3    Wagner, J.4
  • 28
    • 67650526658 scopus 로고    scopus 로고
    • Current and future treatment options for HCV
    • Kronenberger, B., and S. Zeuzem. 2009. Current and future treatment options for HCV. Ann. Hepatol. 8:103-112.
    • (2009) Ann. Hepatol. , vol.8 , pp. 103-112
    • Kronenberger, B.1    Zeuzem, S.2
  • 29
    • 36749001029 scopus 로고    scopus 로고
    • The way forward in HCV treatment - Finding the right path
    • Manns, M. P., et al. 2007. The way forward in HCV treatment - finding the right path. Nat. Rev. Drug Discov. 6:991-1000.
    • (2007) Nat. Rev. Drug Discov. , vol.6 , pp. 991-1000
    • Manns, M.P.1
  • 30
    • 50949096105 scopus 로고    scopus 로고
    • Combinations of cyclophilin inhibitor NIM811 with hepatitis C virus NS3-4A protease or NS5B polymerase inhibitors enhance antiviral activity and suppress the emergence of resistance
    • Mathy, J. E., S. Ma, T. Compton, and K. Lin. 2008. Combinations of cyclophilin inhibitor NIM811 with hepatitis C virus NS3-4A protease or NS5B polymerase inhibitors enhance antiviral activity and suppress the emergence of resistance. Antimicrob. Agents Chemother. 52:3267-3275.
    • (2008) Antimicrob. Agents Chemother. , vol.52 , pp. 3267-3275
    • Mathy, J.E.1    Ma, S.2    Compton, T.3    Lin, K.4
  • 32
    • 67650567074 scopus 로고    scopus 로고
    • Efficacy and safety of the cyclophilin inhibitor DEBIO-025 in combination with pegylated interferon alpha-2A and ribavirin in previously null-responder genotype 1 HCV patients
    • Nelson, D. R., et al. 2009. Efficacy and safety of the cyclophilin inhibitor DEBIO-025 in combination with pegylated interferon alpha-2A and ribavirin in previously null-responder genotype 1 HCV patients. J. Hepatol. 50:S40.
    • (2009) J. Hepatol. , vol.50
    • Nelson, D.R.1
  • 33
    • 33646015668 scopus 로고    scopus 로고
    • The non-immunosuppressive cyclosporin DEBIO-025 is a potent inhibitor of hepatitis C virus replication in vitro
    • Paeshuyse, J., et al. 2006. The non-immunosuppressive cyclosporin DEBIO-025 is a potent inhibitor of hepatitis C virus replication in vitro. Hepatology 43:761-770.
    • (2006) Hepatology , vol.43 , pp. 761-770
    • Paeshuyse, J.1
  • 34
    • 50949132884 scopus 로고    scopus 로고
    • Comparative in vitro anti-hepatitis C virus activities of a selected series of polymerase, protease, and helicase inhibitors
    • Paeshuyse, J., et al. 2008. Comparative in vitro anti-hepatitis C virus activities of a selected series of polymerase, protease, and helicase inhibitors. Antimicrob. Agents Chemother. 52:3433-3437.
    • (2008) Antimicrob. Agents Chemother. , vol.52 , pp. 3433-3437
    • Paeshuyse, J.1
  • 35
    • 36248994744 scopus 로고    scopus 로고
    • Specifically targeted antiviral therapy for hepatitis C virus
    • Parfieniuk, A., J. Jaroszewicz, and R. Flisiak. 2007. Specifically targeted antiviral therapy for hepatitis C virus. World J. Gastroenterol. 13:5673-5681.
    • (2007) World J. Gastroenterol. , vol.13 , pp. 5673-5681
    • Parfieniuk, A.1    Jaroszewicz, J.2    Flisiak, R.3
  • 36
    • 14644402363 scopus 로고    scopus 로고
    • Current and future concepts in hepatitis C therapy
    • Pawlotsky, J. M. 2005. Current and future concepts in hepatitis C therapy. Semin. Liver Dis. 25:72-83.
    • (2005) Semin. Liver Dis. , vol.25 , pp. 72-83
    • Pawlotsky, J.M.1
  • 37
    • 34247895578 scopus 로고    scopus 로고
    • The hepatitis C virus life cycle as a target for new antiviral therapies
    • Pawlotsky, J. M., S. Chevaliez, and J. G. McHutchison. 2007. The hepatitis C virus life cycle as a target for new antiviral therapies. Gastroenterology 132:1979-1998.
    • (2007) Gastroenterology , vol.132 , pp. 1979-1998
    • Pawlotsky, J.M.1    Chevaliez, S.2    McHutchison, J.G.3
  • 38
    • 54149103861 scopus 로고    scopus 로고
    • Emerging therapies for chronic hepatitis C virus
    • Pockros, P. 2008. Emerging therapies for chronic hepatitis C virus. Gastroenterol. Hepatol. 4:729-734.
    • (2008) Gastroenterol. Hepatol. , vol.4 , pp. 729-734
    • Pockros, P.1
  • 40
    • 77951224110 scopus 로고    scopus 로고
    • Mechanism of resistance of hepatitis C virus replicons to structurally distinct cyclophilin inhibitors
    • Puyang, X., et al. 2010. Mechanism of resistance of hepatitis C virus replicons to structurally distinct cyclophilin inhibitors. Antimicrob. Agents Chemother. 54:1981-1987.
    • (2010) Antimicrob. Agents Chemother. , vol.54 , pp. 1981-1987
    • Puyang, X.1
  • 42
    • 34249817897 scopus 로고    scopus 로고
    • Characterization of hepatitis C virus subgenomic replicon resistance to cyclosporine in vitro
    • DOI 10.1128/JVI.02524-06
    • Robida, J. M., H. B. Nelson, Z. Liu, and H. Tang. 2007. Characterization of hepatitis C virus subgenomic replicon resistance to cyclosporine in vitro. J. Virol. 81:5829-5840. (Pubitemid 46847020)
    • (2007) Journal of Virology , vol.81 , Issue.11 , pp. 5829-5840
    • Robida, J.M.1    Nelson, H.B.2    Liu, Z.3    Tang, H.4
  • 43
    • 0032971829 scopus 로고    scopus 로고
    • Sanglifehrins A, B, C and D, novel cyclophilin-binding compounds isolated from Streptomyces sp. A92-308110. I. Taxonomy, fermentation, isolation and biological activity
    • Tokyo
    • Sanglier, J. J., et al. 1999. Sanglifehrins A, B, C and D, novel cyclophilin-binding compounds isolated from Streptomyces sp. A92-308110. I. Taxonomy, fermentation, isolation and biological activity. J. Antibiot. (Tokyo) 52:466-473.
    • (1999) J. Antibiot. , vol.52 , pp. 466-473
    • Sanglier, J.J.1
  • 44
    • 0037414302 scopus 로고    scopus 로고
    • Sanglifehrin-cyclophilin interaction: Degradation work, synthetic macrocyclic analogues, X-ray crystal structure, and binding data
    • Sedrani, R., et al. 2003. Sanglifehrin-cyclophilin interaction: degradation work, synthetic macrocyclic analogues, X-ray crystal structure, and binding data. J. Am. Chem. Soc. 125:3849-3859.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 3849-3859
    • Sedrani, R.1
  • 45
    • 0024844391 scopus 로고
    • Sensitivity to cyclosporin A is mediated by cyclophilin in Neurospora crassa and Saccharomyces cerevisiae
    • DOI 10.1038/342953a0
    • Tropschug, M., I. B. Barthelmess, and W. Neupert. 1989. Sensitivity to cyclosporin A is mediated by cyclophilin in Neurospora crassa and Saccharomyces cerevisiae. Nature 342:953-955. (Pubitemid 20021349)
    • (1989) Nature , vol.342 , Issue.6252 , pp. 953-955
    • Tropschug, M.1    Barthelmess, I.B.2    Neupert, W.3
  • 47
    • 67649206673 scopus 로고    scopus 로고
    • Sequencing of therapy to avoid resistance and the need for new antiretroviral drugs in the treatment of HIV disease
    • Wainberg, M. A., and J. L. Martinez-Cajas. 2009. Sequencing of therapy to avoid resistance and the need for new antiretroviral drugs in the treatment of HIV disease. Infect. Disord. Drug Targets 9:172-190.
    • (2009) Infect. Disord. Drug Targets , vol.9 , pp. 172-190
    • Wainberg, M.A.1    Martinez-Cajas, J.L.2
  • 48
  • 49
    • 77649132408 scopus 로고    scopus 로고
    • Alisporivir, a cyclosporin derivative that selectively inhibits cyclophilin, for the treatment of HCV infection
    • Watashi, K. 2010. Alisporivir, a cyclosporin derivative that selectively inhibits cyclophilin, for the treatment of HCV infection. Curr. Opin. Investig. Drugs 11:213-224.
    • (2010) Curr. Opin. Investig. Drugs , vol.11 , pp. 213-224
    • Watashi, K.1
  • 51
    • 43949123575 scopus 로고    scopus 로고
    • Cyclophilin A is an essential cofactor for hepatitis C virus infection and the principal mediator of cyclosporine resistance in vitro
    • DOI 10.1128/JVI.02614-07
    • Yang, F., et al. 2008. Cyclophilin A is an essential cofactor for hepatitis C virus infection and the principal mediator of cyclosporine resistance in vitro. J. Virol. 82:5269-5278. (Pubitemid 351705235)
    • (2008) Journal of Virology , vol.82 , Issue.11 , pp. 5269-5278
    • Yang, F.1    Robotham, J.M.2    Nelson, H.B.3    Irsigler, A.4    Kenworthy, R.5    Tang, H.6


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