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Volumn 3, Issue 1, 2017, Pages

MMP-7 is a predictive biomarker of disease progression in patients with idiopathic pulmonary fibrosis

Author keywords

[No Author keywords available]

Indexed keywords

BIOLOGICAL MARKER; C PEPTIDE; FAS LIGAND; MATRILYSIN; OSTEOPONTIN; PROCOLLAGEN TYPE I C PEPTIDE; UNCLASSIFIED DRUG;

EID: 85114065337     PISSN: None     EISSN: 23120541     Source Type: Journal    
DOI: 10.1183/23120541.00074-2016     Document Type: Article
Times cited : (87)

References (35)
  • 1
    • 84938125365 scopus 로고    scopus 로고
    • An official ATS/ERS/JRS/ALAT Clinical Practice Guideline: Treatment of idiopathic pulmonary fibrosis. An update of the 2011 Clinical Practice Guideline
    • Raghu G, Rochwerg B, Zhang Y, et al. An official ATS/ERS/JRS/ALAT Clinical Practice Guideline: treatment of idiopathic pulmonary fibrosis. An update of the 2011 Clinical Practice Guideline. Am J Respir Crit Care Med 2015; 192: e3-e19.
    • (2015) Am J Respir Crit Care Med , vol.192 , pp. e3-e19
    • Raghu, G.1    Rochwerg, B.2    Zhang, Y.3
  • 2
    • 84975801947 scopus 로고    scopus 로고
    • Efficacy of nintedanib in idiopathic pulmonary fibrosis across prespecified subgroups in INPULSIS
    • Costabel U, Inoue Y, Richeldi L, et al. Efficacy of nintedanib in idiopathic pulmonary fibrosis across prespecified subgroups in INPULSIS. Am J Respir Crit Care Med 2016; 193: 178-185.
    • (2016) Am J Respir Crit Care Med , vol.193 , pp. 178-185
    • Costabel, U.1    Inoue, Y.2    Richeldi, L.3
  • 3
    • 84954305088 scopus 로고    scopus 로고
    • Pirfenidone for idiopathic pulmonary fibrosis: Analysis of pooled data from three multinational phase 3 trials
    • Noble PW, Albera C, Bradford WZ, et al. Pirfenidone for idiopathic pulmonary fibrosis: analysis of pooled data from three multinational phase 3 trials. Eur Respir J 2016; 47: 243-253.
    • (2016) Eur Respir J , vol.47 , pp. 243-253
    • Noble, P.W.1    Albera, C.2    Bradford, W.Z.3
  • 4
    • 84901817527 scopus 로고    scopus 로고
    • Staging of idiopathic pulmonary fibrosis: Past, present and future
    • Kolb M, Collard HR. Staging of idiopathic pulmonary fibrosis: past, present and future. Eur Respir Rev 2014; 23: 220-224.
    • (2014) Eur Respir Rev , vol.23 , pp. 220-224
    • Kolb, M.1    Collard, H.R.2
  • 5
    • 84855264195 scopus 로고    scopus 로고
    • Peripheral blood proteins predict mortality in idiopathic pulmonary fibrosis
    • Richards TJ, Kaminski N, Baribaud F, et al. Peripheral blood proteins predict mortality in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2012; 185: 67-76.
    • (2012) Am J Respir Crit Care Med , vol.185 , pp. 67-76
    • Richards, T.J.1    Kaminski, N.2    Baribaud, F.3
  • 6
    • 84861162888 scopus 로고    scopus 로고
    • A multidimensional index and staging system for idiopathic pulmonary fibrosis
    • Ley B, Ryerson CJ, Vittinghoff E, et al. A multidimensional index and staging system for idiopathic pulmonary fibrosis. Ann Intern Med 2012; 156: 684-691.
    • (2012) Ann Intern Med , vol.156 , pp. 684-691
    • Ley, B.1    Ryerson, C.J.2    Vittinghoff, E.3
  • 7
    • 84864873409 scopus 로고    scopus 로고
    • Biomarkers in idiopathic pulmonary fibrosis
    • Zhang Y, Kaminski N. Biomarkers in idiopathic pulmonary fibrosis. Curr Opin Pulm Med 2012; 18: 441-446.
    • (2012) Curr Opin Pulm Med , vol.18 , pp. 441-446
    • Zhang, Y.1    Kaminski, N.2
  • 8
    • 84973413713 scopus 로고    scopus 로고
    • Novel approaches to pulmonary fibrosis
    • Jenkins G, Goodwin A. Novel approaches to pulmonary fibrosis. Clin Med 2014; 14: Suppl. 6, s45-s49.
    • (2014) Clin Med , vol.14 , pp. s45-s49
    • Jenkins, G.1    Goodwin, A.2
  • 9
    • 84927920905 scopus 로고    scopus 로고
    • Tissue is an issue in the search for biomarkers in idiopathic pulmonary fibrosis
    • Kaarteenaho R, Lappi-Blanco E. Tissue is an issue in the search for biomarkers in idiopathic pulmonary fibrosis. Fibrogenesis Tissue Repair 2015; 8: 3.
    • (2015) Fibrogenesis Tissue Repair , vol.8 , pp. 3
    • Kaarteenaho, R.1    Lappi-Blanco, E.2
  • 11
    • 80051566676 scopus 로고    scopus 로고
    • BUILD-3: A randomized, controlled trial of bosentan in idiopathic pulmonary fibrosis
    • King TE Jr, Brown KK, Raghu G, et al. BUILD-3: a randomized, controlled trial of bosentan in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2011; 184: 92-99.
    • (2011) Am J Respir Crit Care Med , vol.184 , pp. 92-99
    • King Jr, T.E.1    Brown, K.K.2    Raghu, G.3
  • 12
    • 84856962487 scopus 로고    scopus 로고
    • Enhanced expression of Fas ligand (FasL) in the lower airways of patients with fibrotic interstitial lung diseases (ILDs)
    • Kopinski P, Balicka-Slusarczyk B, Dyczek A, et al. Enhanced expression of Fas ligand (FasL) in the lower airways of patients with fibrotic interstitial lung diseases (ILDs). Folia Histochem Cytobiol 2011; 49: 636-645.
    • (2011) Folia Histochem Cytobiol , vol.49 , pp. 636-645
    • Kopinski, P.1    Balicka-Slusarczyk, B.2    Dyczek, A.3
  • 13
    • 25644460419 scopus 로고    scopus 로고
    • Up-regulation and profibrotic role of osteopontin in human idiopathic pulmonary fibrosis
    • Pardo A, Gibson K, Cisneros J, et al. Up-regulation and profibrotic role of osteopontin in human idiopathic pulmonary fibrosis. PLoS Med 2005; 2: e251.
    • (2005) PLoS Med , vol.2
    • Pardo, A.1    Gibson, K.2    Cisneros, J.3
  • 14
    • 43249084804 scopus 로고    scopus 로고
    • MMP1 and MMP7 as potential peripheral blood biomarkers in idiopathic pulmonary fibrosis
    • Rosas IO, Richards TJ, Konishi K, et al. MMP1 and MMP7 as potential peripheral blood biomarkers in idiopathic pulmonary fibrosis. PLoS Med 2008; 5: e93.
    • (2008) PLoS Med , vol.5
    • Rosas, I.O.1    Richards, T.J.2    Konishi, K.3
  • 15
    • 8144226794 scopus 로고    scopus 로고
    • Idiopathic pulmonary fibrosis: Misunderstandings between epithelial cells and fibroblasts?
    • Selman M, Pardo A. Idiopathic pulmonary fibrosis: misunderstandings between epithelial cells and fibroblasts? Sarcoidosis Vasc Diffuse Lung Dis 2004; 21: 165-172.
    • (2004) Sarcoidosis Vasc Diffuse Lung Dis , vol.21 , pp. 165-172
    • Selman, M.1    Pardo, A.2
  • 16
    • 84893681263 scopus 로고    scopus 로고
    • Idiopathic pulmonary fibrosis: From epithelial injury to biomarkers--insights from the bench side
    • Borensztajn K, Crestani B, Kolb M. Idiopathic pulmonary fibrosis: from epithelial injury to biomarkers--insights from the bench side. Respiration 2013; 86: 441-452.
    • (2013) Respiration , vol.86 , pp. 441-452
    • Borensztajn, K.1    Crestani, B.2    Kolb, M.3
  • 17
    • 84878600828 scopus 로고    scopus 로고
    • Association between the MUC5B promoter polymorphism and survival in patients with idiopathic pulmonary fibrosis
    • Peljto AL, Zhang Y, Fingerlin TE, et al. Association between the MUC5B promoter polymorphism and survival in patients with idiopathic pulmonary fibrosis. JAMA 2013; 309: 2232-2239.
    • (2013) JAMA , vol.309 , pp. 2232-2239
    • Peljto, A.L.1    Zhang, Y.2    Fingerlin, T.E.3
  • 18
    • 0035958935 scopus 로고    scopus 로고
    • Osteopontin, a novel substrate for matrix metalloproteinase-3 (stromelysin-1) and matrix metalloproteinase-7 (matrilysin)
    • Agnihotri R, Crawford HC, Haro H, et al. Osteopontin, a novel substrate for matrix metalloproteinase-3 (stromelysin-1) and matrix metalloproteinase-7 (matrilysin). J Biol Chem 2001; 276: 28261-28267.
    • (2001) J Biol Chem , vol.276 , pp. 28261-28267
    • Agnihotri, R.1    Crawford, H.C.2    Haro, H.3
  • 19
    • 19944406853 scopus 로고    scopus 로고
    • High plasma concentrations of osteopontin in patients with interstitial pneumonia
    • Kadota J, Mizunoe S, Mito K, et al. High plasma concentrations of osteopontin in patients with interstitial pneumonia. Respir Med 2005; 99: 111-117.
    • (2005) Respir Med , vol.99 , pp. 111-117
    • Kadota, J.1    Mizunoe, S.2    Mito, K.3
  • 20
    • 64649089804 scopus 로고    scopus 로고
    • Molecular phenotypes distinguish patients with relatively stable from progressive idiopathic pulmonary fibrosis (IPF)
    • Boon K, Bailey NW, Yang J, et al. Molecular phenotypes distinguish patients with relatively stable from progressive idiopathic pulmonary fibrosis (IPF). PLoS ONE 2009; 4: e5134.
    • (2009) PLoS ONE , vol.4
    • Boon, K.1    Bailey, N.W.2    Yang, J.3
  • 21
    • 0033909857 scopus 로고    scopus 로고
    • Expression of FasL and Fas protein and their soluble form in patients with hypersensitivity pneumonitis
    • Kuwano K, Hagimoto N, Kawasaki M, et al. Expression of FasL and Fas protein and their soluble form in patients with hypersensitivity pneumonitis. Int Arch Allergy Immunol 2000; 122: 209-215.
    • (2000) Int Arch Allergy Immunol , vol.122 , pp. 209-215
    • Kuwano, K.1    Hagimoto, N.2    Kawasaki, M.3
  • 22
    • 0032717522 scopus 로고    scopus 로고
    • Essential roles of the Fas-Fas ligand pathway in the development of pulmonary fibrosis
    • Kuwano K, Hagimoto N, Kawasaki M, et al. Essential roles of the Fas-Fas ligand pathway in the development of pulmonary fibrosis. J Clin Invest 1999; 104: 13-19.
    • (1999) J Clin Invest , vol.104 , pp. 13-19
    • Kuwano, K.1    Hagimoto, N.2    Kawasaki, M.3
  • 23
    • 0033870681 scopus 로고    scopus 로고
    • Soluble form of Fas and Fas ligand in BAL fluid from patients with pulmonary fibrosis and bronchiolitis obliterans organizing pneumonia
    • Kuwano K, Kawasaki M, Maeyama T, et al. Soluble form of Fas and Fas ligand in BAL fluid from patients with pulmonary fibrosis and bronchiolitis obliterans organizing pneumonia. Chest 2000; 118: 451-458.
    • (2000) Chest , vol.118 , pp. 451-458
    • Kuwano, K.1    Kawasaki, M.2    Maeyama, T.3
  • 24
    • 84928585996 scopus 로고    scopus 로고
    • Cutting edge: FasL+ immune cells promote resolution of fibrosis
    • Wallach-Dayan SB, Elkayam L, Golan-Gerstl R, et al. Cutting edge: FasL+ immune cells promote resolution of fibrosis. J Autoimmun 2015; 59: 67-76.
    • (2015) J Autoimmun , vol.59 , pp. 67-76
    • Wallach-Dayan, S.B.1    Elkayam, L.2    Golan-Gerstl, R.3
  • 25
    • 77955303165 scopus 로고    scopus 로고
    • Myocardial fibrosis as an early manifestation of hypertrophic cardiomyopathy
    • Ho CY, Lopez B, Coelho-Filho OR, et al. Myocardial fibrosis as an early manifestation of hypertrophic cardiomyopathy. N Engl J Med 2010; 363: 552-563.
    • (2010) N Engl J Med , vol.363 , pp. 552-563
    • Ho, C.Y.1    Lopez, B.2    Coelho-Filho, O.R.3
  • 26
    • 0026536442 scopus 로고
    • Serum procollagen peptides and collagen type VI for the assessment of activity and degree of hepatic fibrosis in schistosomiasis and alcoholic liver disease
    • Shahin M, Schuppan D, Waldherr R, et al. Serum procollagen peptides and collagen type VI for the assessment of activity and degree of hepatic fibrosis in schistosomiasis and alcoholic liver disease. Hepatology 1992; 15: 637-644.
    • (1992) Hepatology , vol.15 , pp. 637-644
    • Shahin, M.1    Schuppan, D.2    Waldherr, R.3
  • 27
    • 29644447894 scopus 로고    scopus 로고
    • T-helper-2 cytokine responses to Sj97 predict resistance to reinfection with Schistosoma japonicum
    • Leenstra T, Acosta LP, Wu HW, et al. T-helper-2 cytokine responses to Sj97 predict resistance to reinfection with Schistosoma japonicum. Infect Immun 2006; 74: 370-381.
    • (2006) Infect Immun , vol.74 , pp. 370-381
    • Leenstra, T.1    Acosta, L.P.2    Wu, H.W.3
  • 28
    • 79751476612 scopus 로고    scopus 로고
    • Tissue inhibitor of matrix-metalloprotease-1 predicts risk of hepatic fibrosis in human Schistosoma japonicum infection
    • Fabre V, Wu H, PondTor S, et al. Tissue inhibitor of matrix-metalloprotease-1 predicts risk of hepatic fibrosis in human Schistosoma japonicum infection. J Infect Dis 2011; 203: 707-714.
    • (2011) J Infect Dis , vol.203 , pp. 707-714
    • Fabre, V.1    Wu, H.2    PondTor, S.3
  • 30
    • 79961117116 scopus 로고    scopus 로고
    • Multisite comparison of high-sensitivity multiplex cytokine assays
    • Breen EC, Reynolds SM, Cox C, et al. Multisite comparison of high-sensitivity multiplex cytokine assays. Clin Vaccine Immunol 2011; 18: 1229-1242.
    • (2011) Clin Vaccine Immunol , vol.18 , pp. 1229-1242
    • Breen, E.C.1    Reynolds, S.M.2    Cox, C.3
  • 31
    • 82755161052 scopus 로고    scopus 로고
    • Idiopathic pulmonary fibrosis
    • King TE Jr, Pardo A, Selman M. Idiopathic pulmonary fibrosis. Lancet 2011; 378: 1949-1961.
    • (2011) Lancet , vol.378 , pp. 1949-1961
    • King Jr, T.E.1    Pardo, A.2    Selman, M.3
  • 32
    • 84924361457 scopus 로고    scopus 로고
    • The effectiveness and cost-effectiveness of treatments for idiopathic pulmonary fibrosis: Systematic review, network meta-analysis and health economic evaluation
    • Loveman E, Copley VR, Colquitt JL, et al. The effectiveness and cost-effectiveness of treatments for idiopathic pulmonary fibrosis: systematic review, network meta-analysis and health economic evaluation. BMC Pharmacol Toxicol 2014; 15: 63.
    • (2014) BMC Pharmacol Toxicol , vol.15 , pp. 63
    • Loveman, E.1    Copley, V.R.2    Colquitt, J.L.3
  • 33
    • 84998814253 scopus 로고    scopus 로고
    • Plasma surfactant protein-D, matrix metalloproteinase-7, and osteopontin index distinguishes idiopathic pulmonary fibrosis from other idiopathic interstitial pneumonias
    • White ES, Xia M, Murray S, et al. Plasma surfactant protein-D, matrix metalloproteinase-7, and osteopontin index distinguishes idiopathic pulmonary fibrosis from other idiopathic interstitial pneumonias. Am J Respir Crit Care Med 2016; 194: 1242-1251.
    • (2016) Am J Respir Crit Care Med , vol.194 , pp. 1242-1251
    • White, E.S.1    Xia, M.2    Murray, S.3
  • 34
    • 84902249499 scopus 로고    scopus 로고
    • Evidence-based detection of pulmonary arterial hypertension in systemic sclerosis: The DETECT study
    • Coghlan JG, Denton CP, Grunig E, et al. Evidence-based detection of pulmonary arterial hypertension in systemic sclerosis: the DETECT study. Ann Rheum Dis 2014; 73: 1340-1349.
    • (2014) Ann Rheum Dis , vol.73 , pp. 1340-1349
    • Coghlan, J.G.1    Denton, C.P.2    Grunig, E.3
  • 35
    • 84930865108 scopus 로고    scopus 로고
    • Longitudinal change in collagen degradation biomarkers in idiopathic pulmonary fibrosis: An analysis from the prospective, multicentre PROFILE study
    • Jenkins RG, Simpson JK, Saini G, et al. Longitudinal change in collagen degradation biomarkers in idiopathic pulmonary fibrosis: an analysis from the prospective, multicentre PROFILE study. Lancet Respir Med 2015; 3: 462-472.
    • (2015) Lancet Respir Med , vol.3 , pp. 462-472
    • Jenkins, R.G.1    Simpson, J.K.2    Saini, G.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.