Results 1 to 10 of about 22,445 (222)

Transcription factor Sp1 induces ADAM17 and contributes to tumor cell invasiveness under hypoxia [PDF]

open access: yesJournal of Experimental & Clinical Cancer Research, 2009
Background Expression of the Sp1 transcription factor is induced by hypoxia, and the ADAM17 promoter contains predicted Sp1 binding sites. ADAM17 contributes to hypoxic-induce invasiveness of glioma.
Jiang Feng   +4 more
doaj   +4 more sources

Strategies to Target ADAM17 in Disease: From Its Discovery to the iRhom Revolution

open access: yesMolecules, 2021
For decades, disintegrin and metalloproteinase 17 (ADAM17) has been the object of deep investigation. Since its discovery as the tumor necrosis factor convertase, it has been considered a major drug target, especially in the context of inflammatory ...
Doretta Cuffaro   +2 more
exaly   +3 more sources

ADAM17-dependent Autocrine and Paracrine Signaling Promotes Pancreatic Premalignant ProgressionSummaryWhat You Need to Know [PDF]

open access: yesCellular and Molecular Gastroenterology and Hepatology
Background & Aims: A Disintegrin and Metalloproteinase 17 (ADAM17) is a membrane-bound sheddase that regulates the release of multiple signaling molecules, including inflammatory mediators and epidermal growth factor receptor (EGFR) ligands.
Hui-Ju Wen   +14 more
doaj   +2 more sources

ADAM17 as a promising therapeutic target: from structural basis to inhibitor discovery in human diseases [PDF]

open access: yesFrontiers in Pharmacology
A disintegrin and metalloproteinase 17 (ADAM17) is a transmembrane protease that regulates diverse physiological processes by shedding membrane-bound proteins, including cytokines, their receptors, and adhesion molecules.
Lisa Liu   +8 more
doaj   +2 more sources

Targeting ADAM17 to dampen dendritic cell-mediated type 2 immune responses and airway inflammation associated with allergic asthma [PDF]

open access: yesScientific Reports
The zinc containing matrix metalloproteinase enzyme regulates a diverse array of biological processes in health and disease, including ADAM17 (a disintegrin and metalloproteinase domain 17) enzyme.
Anil Kumar Jaiswal   +2 more
doaj   +2 more sources

ADAM17 knockdown mitigates while ADAM17 overexpression aggravates cardiac fibrosis and dysfunction via regulating ACE2 shedding and myofibroblast transformation

open access: yesFrontiers in Pharmacology, 2022
A disintegrin and metalloprotease domain family protein 17 (ADAM17) is a new member of renin-angiotensin system (RAS) but its role in the pathogenesis of diabetic cardiomyopathy (DCM) is obscure.
Jing Cheng   +20 more
doaj   +1 more source

ADAM Metalloproteinase Domain 17 Regulates Cholestasis-Associated Liver Injury and Sickness Behavior Development in Mice

open access: yesFrontiers in Immunology, 2022
Disintegrin and metalloproteinase domain-containing protein 17 (ADAM17) is a ubiquitously expressed membrane-bound enzyme that mediates shedding of a wide variety of important regulators in inflammation including cytokines and adhesion molecules. Hepatic
Wagdi Almishri   +7 more
doaj   +1 more source

Immunomodulatory role of metalloproteinase ADAM17 in tumor development

open access: yesFrontiers in Immunology, 2022
ADAM17 is a member of the a disintegrin and metalloproteinase (ADAM) family of transmembrane proteases involved in the shedding of some cell membrane proteins and regulating various signaling pathways.
Kai Wang   +5 more
doaj   +1 more source

Tetraspanin 8 Subfamily Members Regulate Substrate-Specificity of a Disintegrin and Metalloprotease 17

open access: yesCells, 2022
Ectodomain shedding is an irreversible process to regulate inter- and intracellular signaling. Members of the a disintegrin and metalloprotease (ADAM) family are major mediators of ectodomain shedding.
Miryam Müller   +10 more
doaj   +1 more source

ADAM17 silencing in mouse colon carcinoma cells: the effect on tumoricidal cytokines and angiogenesis. [PDF]

open access: yesPLoS ONE, 2012
ADAM17 (a disintegrin and metalloprotease 17) is a major sheddase for numerous growth factors, cytokines, receptors, and cell adhesion molecules and is often overexpressed in malignant cells.
Sudipta Das   +13 more
doaj   +1 more source

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