메뉴 건너뛰기




Volumn 88, Issue 4, 2015, Pages 791-799

Potentiators of defective DF508-CFTR gating that do not interfere with corrector action

Author keywords

[No Author keywords available]

Indexed keywords

1 (2,2 DIFLUORO 1,3 BENZODIOXOL 5 YL) N [1 (2,3 DIHYDROXYPROPYL) 6 FLUORO 2 (2 HYDROXY 1,1 DIMETHYLETHYL) 1H INDOL 5 YL]CYCLOPROPANECARBOXAMIDE; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; GENISTEIN; ISOXAZOLE DERIVATIVE; IVACAFTOR; LUMACAFTOR; PYRAZOLE; PYRROLE; 1,3 BENZODIOXOLE DERIVATIVE; AMINOPYRIDINE DERIVATIVE; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR DELTA F508;

EID: 84946402384     PISSN: 0026895X     EISSN: 15210111     Source Type: Journal    
DOI: 10.1124/mol.115.099689     Document Type: Article
Times cited : (35)

References (33)
  • 1
    • 79551596804 scopus 로고    scopus 로고
    • Therapeutics development for cystic fibrosis: A successful model for a multisystem genetic disease
    • Ashlock MA and Olson ER (2011) Therapeutics development for cystic fibrosis: A successful model for a multisystem genetic disease. Annu Rev Med 62:107-125.
    • (2011) Annu Rev Med , vol.62 , pp. 107-125
    • Ashlock, M.A.1    Olson, E.R.2
  • 2
    • 0346505482 scopus 로고    scopus 로고
    • New concepts of the pathogenesis of cystic fibrosis lung disease
    • Boucher RC (2004) New concepts of the pathogenesis of cystic fibrosis lung disease. Eur Respir J 23:146-158.
    • (2004) Eur Respir J , vol.23 , pp. 146-158
    • Boucher, R.C.1
  • 3
    • 84904002908 scopus 로고    scopus 로고
    • A CFTR corrector (lumacaftor) and a CFTR potentiator (ivacaftor) for treatment of patients with cystic fibrosis who have a phe508del CFTR mutation: A phase 2 randomised controlled trial
    • VX09-809-102 study group
    • Boyle MP, Bell SC, Konstan MW, McColley SA, Rowe SM, Rietschel E, Huang X, Waltz D, Patel NR, and Rodman D; VX09-809-102 study group (2014) A CFTR corrector (lumacaftor) and a CFTR potentiator (ivacaftor) for treatment of patients with cystic fibrosis who have a phe508del CFTR mutation: A phase 2 randomised controlled trial. Lancet Respir Med 2:527-538.
    • (2014) Lancet Respir Med , vol.2 , pp. 527-538
    • Boyle, M.P.1    Bell, S.C.2    Konstan, M.W.3    McColley, S.A.4    Rowe, S.M.5    Rietschel, E.6    Huang, X.7    Waltz, D.8    Patel, N.R.9    Rodman, D.10
  • 4
  • 5
    • 84856229740 scopus 로고    scopus 로고
    • Identification of important structural features of thiazolo[4, 5-d]pyrimidines required for potent antifungal activity
    • Chhabria M, Rathod I, Vala K, and Patel P (2011) Identification of important structural features of thiazolo[4, 5-d]pyrimidines required for potent antifungal activity. Med Chem Res 20:1450-1454.
    • (2011) Med Chem Res , vol.20 , pp. 1450-1454
    • Chhabria, M.1    Rathod, I.2    Vala, K.3    Patel, P.4
  • 7
    • 0026523829 scopus 로고
    • Cystic fibrosis: Molecular biology and therapeutic implications
    • Collins FS (1992) Cystic fibrosis: molecular biology and therapeutic implications. Science 256:774-779.
    • (1992) Science , vol.256 , pp. 774-779
    • Collins, F.S.1
  • 8
    • 33645130994 scopus 로고    scopus 로고
    • Cystic fibrosis since 1938
    • Davis PB (2006) Cystic fibrosis since 1938. Am J Respir Crit Care Med 173:475-482.
    • (2006) Am J Respir Crit Care Med , vol.173 , pp. 475-482
    • Davis, P.B.1
  • 10
    • 32444436992 scopus 로고    scopus 로고
    • Towards an in vitro model of cystic fibrosis small airway epithelium: Characterisation of the human bronchial epithelial cell line CFBE41o
    • Ehrhardt C, Collnot EM, Baldes C, Becker U, Laue M, Kim KJ, and Lehr CM (2006) Towards an in vitro model of cystic fibrosis small airway epithelium: characterisation of the human bronchial epithelial cell line CFBE41o-. Cell Tissue Res 323: 405-415.
    • (2006) Cell Tissue Res , vol.323 , pp. 405-415
    • Ehrhardt, C.1    Collnot, E.M.2    Baldes, C.3    Becker, U.4    Laue, M.5    Kim, K.J.6    Lehr, C.M.7
  • 11
    • 84870502577 scopus 로고    scopus 로고
    • Human nasal and tracheo-bronchial respiratory epithelial cell culture
    • Fulcher ML and Randell SH (2013) Human nasal and tracheo-bronchial respiratory epithelial cell culture. Methods Mol Biol 945:109-121.
    • (2013) Methods Mol Biol , vol.945 , pp. 109-121
    • Fulcher, M.L.1    Randell, S.H.2
  • 12
    • 0035933577 scopus 로고    scopus 로고
    • Green fluorescent protein-based halide indicators with improved chloride and iodide affinities
    • Galietta LJ, Haggie PM, and Verkman AS (2001) Green fluorescent protein-based halide indicators with improved chloride and iodide affinities. FEBS Lett 499: 220-224.
    • (2001) FEBS Lett , vol.499 , pp. 220-224
    • Galietta, L.J.1    Haggie, P.M.2    Verkman, A.S.3
  • 13
    • 84873397801 scopus 로고    scopus 로고
    • Novel pharmacological strategies to treat cystic fibrosis
    • Hanrahan JW, Sampson HM, and Thomas DY (2013) Novel pharmacological strategies to treat cystic fibrosis. Trends Pharmacol Sci 34:119-125.
    • (2013) Trends Pharmacol Sci , vol.34 , pp. 119-125
    • Hanrahan, J.W.1    Sampson, H.M.2    Thomas, D.Y.3
  • 14
    • 84946601734 scopus 로고    scopus 로고
    • inventors, Ito M, Suzaki T, Takeda Pharmaceutical, Yamamoto S, assignee. Substituted pyrazole derivative. Patent. 2009 Mar 5
    • Ito M, Suzaki T, Yamamoto S (2009) inventors, Ito M, Suzaki T, Takeda Pharmaceutical, Yamamoto S, assignee. Substituted pyrazole derivative. Patent WO2009028543 A1. 2009 Mar 5.
    • (2009)
    • Ito, M.1    Suzaki, T.2    Yamamoto, S.3
  • 15
    • 0037020097 scopus 로고    scopus 로고
    • High-affinity activators of cystic fibrosis transmembrane conductance regulator (CFTR) chloride conductance identified by high-throughput screening
    • Ma T, Vetrivel L, Yang H, Pedemonte N, Zegarra-Moran O, Galietta LJ, and Verkman AS (2002) High-affinity activators of cystic fibrosis transmembrane conductance regulator (CFTR) chloride conductance identified by high-throughput screening. J Biol Chem 277:37235-37241.
    • (2002) J Biol Chem , vol.277 , pp. 37235-37241
    • Ma, T.1    Vetrivel, L.2    Yang, H.3    Pedemonte, N.4    Zegarra-Moran, O.5    Galietta, L.J.6    Verkman, A.S.7
  • 17
    • 84946601735 scopus 로고    scopus 로고
    • Inventors, pharmacia corporation, assignee
    • U.S. patent. 2005 Dec 27
    • Naraian AS, et al. (2005) inventors, Pharmacia Corporation, assignee. Substituted pyrazoles as p38 kinase inhibitors. U.S. patent 6979686 B1. 2005 Dec 27.
    • (2005) Substituted Pyrazoles as P38 Kinase Inhibitors
    • Naraian, A.S.1
  • 19
    • 84883377550 scopus 로고    scopus 로고
    • Development, clinical utility, and place of ivacaftor in the treatment of cystic fibrosis
    • O'Reilly R and Elphick HE (2013) Development, clinical utility, and place of ivacaftor in the treatment of cystic fibrosis. Drug Des Devel Ther 7:929-937.
    • (2013) Drug des Devel Ther , vol.7 , pp. 929-937
    • O'Reilly, R.1    Elphick, H.E.2
  • 20
    • 84879000844 scopus 로고    scopus 로고
    • Cystic fibrosis transmembrane regulator correctors and potentiators
    • Rowe SM and Verkman AS (2013) Cystic fibrosis transmembrane regulator correctors and potentiators. Cold Spring Harb Perspect Med 3:a009761.
    • (2013) Cold Spring Harb Perspect Med , vol.3 , pp. a009761
    • Rowe, S.M.1    Verkman, A.S.2
  • 23
    • 84901453811 scopus 로고    scopus 로고
    • Synergy-based small-molecule screen using a human lung epithelial cell line yields DF508-CFTR correctors that augment VX-809 maximal efficacy
    • Phuan PW, Veit G, Tan J, Roldan A, Finkbeiner WE, Lukacs GL, and Verkman AS (2014) Synergy-based small-molecule screen using a human lung epithelial cell line yields DF508-CFTR correctors that augment VX-809 maximal efficacy. Mol Pharmacol 86:42-51.
    • (2014) Mol Pharmacol , vol.86 , pp. 42-51
    • Phuan, P.W.1    Veit, G.2    Tan, J.3    Roldan, A.4    Finkbeiner, W.E.5    Lukacs, G.L.6    Verkman, A.S.7
  • 25
    • 50649123290 scopus 로고    scopus 로고
    • CFTR function and prospects for therapy
    • Riordan JR (2008) CFTR function and prospects for therapy. Annu Rev Biochem 77: 701-726.
    • (2008) Annu Rev Biochem , vol.77 , pp. 701-726
    • Riordan, J.R.1
  • 27
    • 42149120706 scopus 로고    scopus 로고
    • Phenylalanine-508 mediates a cytoplasmic-membrane domain contact in the CFTR 3D structure crucial to assembly and channel function
    • Serohijos AW, Hegedus T, Aleksandrov AA, He L, Cui L, Dokholyan NV, and Riordan JR (2008) Phenylalanine-508 mediates a cytoplasmic-membrane domain contact in the CFTR 3D structure crucial to assembly and channel function. Proc Natl Acad Sci USA 105:3256-3261.
    • (2008) Proc Natl Acad Sci USA , vol.105 , pp. 3256-3261
    • Serohijos, A.W.1    Hegedus, T.2    Aleksandrov, A.A.3    He, L.4    Cui, L.5    Dokholyan, N.V.6    Riordan, J.R.7
  • 31
    • 84868255280 scopus 로고    scopus 로고
    • Proinflammatory cytokine secretion is suppressed by TMEM16A or CFTR channel activity in human cystic fibrosis bronchial epithelia
    • Veit G, Bossard F, Goepp J, Verkman AS, Galietta LJ, Hanrahan JW, and Lukacs GL (2012) Proinflammatory cytokine secretion is suppressed by TMEM16A or CFTR channel activity in human cystic fibrosis bronchial epithelia. Mol Biol Cell 23:4188-4202.
    • (2012) Mol Biol Cell , vol.23 , pp. 4188-4202
    • Veit, G.1    Bossard, F.2    Goepp, J.3    Verkman, A.S.4    Galietta, L.J.5    Hanrahan, J.W.6    Lukacs, G.L.7
  • 32
    • 0026636673 scopus 로고
    • Differentiated structure and function of cultures from human tracheal epithelium
    • Yamaya M, Finkbeiner WE, Chun SY, and Widdicombe JH (1992) Differentiated structure and function of cultures from human tracheal epithelium. Am J Physiol 262:L713-L724.
    • (1992) Am J Physiol , vol.262 , pp. L713-L724
    • Yamaya, M.1    Finkbeiner, W.E.2    Chun, S.Y.3    Widdicombe, J.H.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.