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Inflammation and Fibrosis in ADPKD

Authors
Mun, HyowonPark, Jong Hoon
Issue Date
Oct-2016
Publisher
SPRINGER-VERLAG SINGAPORE PTE LTD
Keywords
Inflammation; Fibrosis; Polycystic kidney disease; Macrophage; TNF-alpha; TGF-beta
Citation
CYSTOGENESIS, v.933, pp 35 - 44
Pages
10
Journal Title
CYSTOGENESIS
Volume
933
Start Page
35
End Page
44
URI
https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/9407
DOI
10.1007/978-981-10-2041-4_4
ISSN
0065-2598
2214-8019
Abstract
Diverse signaling pathways have been reported to be associated with polycystic kidney disease (PKD). Cell proliferation is widely known to be an important pathway related to this disease. However, studies on the interactions of inflammation and fibrosis with polycystic kidney disease have been limited. Inflammation is one of the protective systems involved in the response to foreign molecules. In PKD, it was reported that the activity of signaling pathways associated with inflammation is increased. Also, fibrosis is the development of excess fibrous tissue in organ or tissue. It is an abnormal phenomenon in which the extent of fibrous connective tissues is increased. In PKD, increases in the activity of molecules such as growth factor and TGF-beta have been reported to occur and promote fibrosis. Therefore, the inflammation and fibrosis responses have been suggested as therapeutic targets for PKD. In order to guide further studies, this review indicates the roles of inflammatory and fibrosis signaling in PKD.
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