@article {Ma:2011:1872-3136:44,
title = "The Role of STAT 3 in Tissue Fibrosis",
journal = "Current Chemical Biology",
parent_itemid = "infobike://ben/ccb",
publishercode ="ben",
year = "2011",
volume = "5",
number = "1",
publication date ="2011-01-01T00:00:00",
pages = "44-51",
itemtype = "ARTICLE",
issn = "1872-3136",
url = "https://www.ingentaconnect.com/content/ben/ccb/2011/00000005/00000001/art00006",
doi = "doi:10.2174/187231311793564342",
keyword = "hypertension, diabetic, nephron, STAT3, traumatic injuries, visceral epithelium, hyperfiltration, fibroblasts, phosphorylation, fibroproliferative diseases, aging, smooth actin, central nervous system, obstructive nephropathy, migration, IgA, fibrogenic actions, cytoplasmic transcription, epithelial cells, Astrocytes, leukocytes, hardening, carbon tetrachlorideinduced, bleomycin injury, parasitic diseases, skin lesions, proliferation, growth factor, (TGF), myocardial infarction, Idiopathic pulmonary fibrosis (IPF), cytokines/growth factors, glomerular sclerosis, collagen deposition, protein-protein interactions, urinary albumin excretion, organ failure, neutrophils, extracellular matrix, unilateral ureteral obstruction (UUO), tissue fibrosis, tyrosine kinase, oxidative stress, DNA binding, platelet derived growth factor (PDGF), allergic responses, glial cells, cytokines, syndrome, Spinal Cord Injury, inflammatory cells, glomerulonephritis, kidney, Keloid, hemodynamic, hepatic stellate cells, cirrhosis, hyperactivation, pathogenesis of tissue, Receptors, bone marrow, chronic autoimmune diseases or rachitis, hematopoetic factors, metabolic disorders, Immunofluorescence, motor recovery, Renal Interstitial Fibrosis, C-terminal transactivation, myeloid metaplasia, interstitial edema, coiled-coil, autoimmune",
author = "Ma, Li and Zhuang, Shougang",
abstract = "Signal transducer and activator of transcription 3 (STAT3) is a transcriptional factor and has been implicated in cell proliferation, survival and differentiation. Recent studies demonstrate that STAT3 activity is persistently elevated in patients with some chronic disorders, and required for the development and progression of fibrosis in a variety of tissues including kidney, bone marrow and skin. On the other hand, STAT3 is implicated in tissue protection against fibrosis in the heart following acute injury. Moreover, STAT3 can either promote or protect against tissue fibrosis in chronic liver disease models, depending on etiologies. The underlying mechanisms by which STAT3 mediates those cellular events are not fully understood, but the profibrotic action of STAT3 is mostly associated with activation and proliferation of fibroblasts, deposition of excessive extracellular matrix proteins, and overproduction of some cytokines. In this review article, we discuss the role of STAT3 in tissue fibrosis and the effect of the STAT3 pathway inhibition on the proliferation and activation of fibroblasts in vitro and fibrogenesis in various animal models. ",
}