Epithelial cell-derived cytokines CST3 and GDF15 as potential therapeutics for pulmonary fibrosis
暂无分享,去创建一个
D. Chung | C. Cho | J. Koh | Hyun-Woo Shin | Jong-Wan Park | Y. Chun | Young-Im Kim
[1] A. Hajari Case,et al. Clinical use of nintedanib in patients with idiopathic pulmonary fibrosis , 2017, BMJ Open Respiratory Research.
[2] K. Meyer,et al. Role of pirfenidone in the management of pulmonary fibrosis , 2017, Therapeutics and clinical risk management.
[3] A. Kaneda,et al. Combined Secretomics and Transcriptomics Revealed Cancer-Derived GDF15 is Involved in Diffuse-Type Gastric Cancer Progression and Fibroblast Activation , 2016, Scientific Reports.
[4] M. Nakazato,et al. Breakdown of Epithelial Barrier Integrity and Overdrive Activation of Alveolar Epithelial Cells in the Pathogenesis of Acute Respiratory Distress Syndrome and Lung Fibrosis , 2015, BioMed research international.
[5] K. Tsui,et al. Growth differentiation factor-15: a p53- and demethylation-upregulating gene represses cell proliferation, invasion, and tumorigenesis in bladder carcinoma cells , 2015, Scientific Reports.
[6] C. Ruppert,et al. Compromised peroxisomes in idiopathic pulmonary fibrosis, a vicious cycle inducing a higher fibrotic response via TGF-β signaling , 2015, Proceedings of the National Academy of Sciences.
[7] Efficacy and Safety of Nintedanib in Idiopathic Pulmonary Fibrosis. , 2015, The New England journal of medicine.
[8] Chun Xing Li,et al. Treatment with CA-074Me, a Cathepsin B inhibitor, reduces lung interstitial inflammation and fibrosis in a rat model of polymyositis , 2014, Laboratory Investigation.
[9] H. Collard,et al. Design of the INPULSIS™ trials: two phase 3 trials of nintedanib in patients with idiopathic pulmonary fibrosis. , 2014, Respiratory medicine.
[10] S. Marchand-Adam,et al. Regulation of TGF-β1-driven Differentiation of Human Lung Fibroblasts , 2014, The Journal of Biological Chemistry.
[11] S. Rosselot. Idiopathic pulmonary fibrosis. , 2014, Nursing standard (Royal College of Nursing (Great Britain) : 1987).
[12] M. Syamsunarno,et al. Deranged fatty acid composition causes pulmonary fibrosis in Elovl6-deficient mice , 2013, Nature Communications.
[13] S. Friedman,et al. Therapy for Fibrotic Diseases: Nearing the Starting Line , 2013, Science Translational Medicine.
[14] T. Meuten,et al. WNT7B in fibroblastic foci of idiopathic pulmonary fibrosis , 2012, Respiratory Research.
[15] Y. Yamaguchi,et al. A Peptide Derived from Endostatin Ameliorates Organ Fibrosis , 2012, Science Translational Medicine.
[16] Jong-Wha Jung,et al. Design, synthesis and insight into the structure-activity relationship of 1,3-disubstituted indazoles as novel HIF-1 inhibitors. , 2011, Bioorganic & Medicinal Chemistry Letters.
[17] R. D. du Bois,et al. Pirfenidone in idiopathic pulmonary fibrosis: the CAPACITY program , 2011, Expert review of respiratory medicine.
[18] D. Fairclough,et al. Pirfenidone in idiopathic pulmonary fibrosis , 2010, European Respiratory Journal.
[19] T. Chou. Drug combination studies and their synergy quantification using the Chou-Talalay method. , 2010, Cancer research.
[20] G. Raghu,et al. Pirfenidone in idiopathic pulmonary fibrosis , 2009, European Respiratory Journal.
[21] S. Sahn,et al. Effect of interferon gamma-1b on survival in patients with idiopathic pulmonary fibrosis (INSPIRE): a multicentre, randomised, placebo-controlled trial , 2009, The Lancet.
[22] F. Hilberg,et al. Design, synthesis, and evaluation of indolinones as triple angiokinase inhibitors and the discovery of a highly specific 6-methoxycarbonyl-substituted indolinone (BIBF 1120). , 2009, Journal of medicinal chemistry.
[23] A. Moles,et al. Cathepsins B and D drive hepatic stellate cell proliferation and promote their fibrogenic potential , 2009, Hepatology.
[24] H. Bolte,et al. Standardized quantification of pulmonary fibrosis in histological samples. , 2008, BioTechniques.
[25] D. Warburton,et al. The bleomycin animal model: a useful tool to investigate treatment options for idiopathic pulmonary fibrosis? , 2008, The international journal of biochemistry & cell biology.
[26] G. Amir,et al. Epithelial cell apoptosis by fas ligand-positive myofibroblasts in lung fibrosis. , 2007, American journal of respiratory cell and molecular biology.
[27] A. Schnapp,et al. Pharmacologic differentiation of inflammation and fibrosis in the rat bleomycin model. , 2006, American journal of respiratory and critical care medicine.
[28] R. Lotan,et al. Induction of GDF-15/NAG-1/MIC-1 in human lung carcinoma cells by retinoid-related molecules and assessment of Its role in apoptosis , 2006, Cancer Biology & Therapy.
[29] Katsutoshi Nakayama,et al. Anticoagulant therapy for idiopathic pulmonary fibrosis. , 2005, Chest.
[30] W. Schiemann,et al. The use of cystatin C to inhibit epithelial–mesenchymal transition and morphological transformation stimulated by transforming growth factor-β , 2005, Breast Cancer Research.
[31] Mehdi Ahmadi,et al. Evaluation of EM and orthopedic residents' pain estimation about patients with limb trauma who were visited in the Emergency Department of Hazrat Rasoul Hospital , 2005 .
[32] P. Villa,et al. Serum cystatin C concentration as a marker of acute renal dysfunction in critically ill patients , 2005, Critical care.
[33] W. Schiemann,et al. Cystatin C antagonizes transforming growth factor beta signaling in normal and cancer cells. , 2004, Molecular cancer research : MCR.
[34] J. Zaunders,et al. Macrophage inhibitory cytokine 1 reduces cell adhesion and induces apoptosis in prostate cancer cells. , 2003, Cancer research.
[35] G. Gores,et al. Cathepsin B inactivation attenuates hepatic injury and fibrosis during cholestasis. , 2003, The Journal of clinical investigation.
[36] G. Gabbiani,et al. The myofibroblast in wound healing and fibrocontractive diseases , 2003, The Journal of pathology.
[37] W. Thurlbeck,et al. Idiopathic pulmonary fibrosis: relationship between histopathologic features and mortality. , 2001, American journal of respiratory and critical care medicine.
[38] K. Flaherty,et al. Corticosteroids in idiopathic pulmonary fibrosis , 2001, Current opinion in pulmonary medicine.
[39] B. Kobilka,et al. Functional differences between full and partial agonists: evidence for ligand-specific receptor conformations. , 2001, The Journal of pharmacology and experimental therapeutics.
[40] G. Raghu,et al. Treatment of Idiopathic Pulmonary Fibrosis with a New Antifibrotic Agent , Pirfenidone Results of a Prospective , Open-label Phase II Study , 1999 .
[41] S. Swensen,et al. Colchicine versus prednisone in the treatment of idiopathic pulmonary fibrosis. A randomized prospective study. Members of the Lung Study Group. , 1998, American journal of respiratory and critical care medicine.
[42] T. Urano,et al. Tissue factor expression and fibrin deposition in the lungs of patients with idiopathic pulmonary fibrosis and systemic sclerosis. , 1997, American journal of respiratory and critical care medicine.
[43] G. Raghu,et al. Azathioprine combined with prednisone in the treatment of idiopathic pulmonary fibrosis: a prospective double-blind, randomized, placebo-controlled clinical trial. , 1991, The American review of respiratory disease.