2023
DOI: 10.1111/febs.16923
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The protease ADAM17 at the crossroads of disease: revisiting its significance in inflammation, cancer, and beyond

Abstract: The protease A Disintegrin And Metalloproteinase 17 (ADAM17) plays a central role in the pathophysiology of several diseases. ADAM17 is involved in the cleavage and shedding of at least 80 known membrane‐tethered proteins, which subsequently modulate several intracellular signaling pathways, and therefore alter cell behavior. Dysregulated expression and/or activation of ADAM17 has been linked to a wide range of autoimmune and inflammatory diseases, cancer and cardiovascular disease. In this review, we provide … Show more

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Cited by 15 publications
(10 citation statements)
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“…Increased expression of inflammatory mediators, such as Adam17 (Figure 4D), an inflammatory protease that cleaves numerous cell membrane cytokines and receptors, including the TAM receptor MERTK (19)(20)(21)(22). Cleavage of MERTK results in reduced phagocytotic clearance of apoptotic cells and pro-inflammatory nucleic acids (19,23,24).…”
Section: Immunolocalization Of Rmpmentioning
confidence: 99%
“…Increased expression of inflammatory mediators, such as Adam17 (Figure 4D), an inflammatory protease that cleaves numerous cell membrane cytokines and receptors, including the TAM receptor MERTK (19)(20)(21)(22). Cleavage of MERTK results in reduced phagocytotic clearance of apoptotic cells and pro-inflammatory nucleic acids (19,23,24).…”
Section: Immunolocalization Of Rmpmentioning
confidence: 99%
“…Second, we developed two distinct including growth factors, cytokines, receptors, and cell adhesion molecules. It plays a pivotal role in intracellular signaling pathways related to inflammation and angiogenesis [52][53][54][55]. By analyzing a publicly available scRNA-seq (Drop-seq) dataset (GSE150703) that compared OIR and normal conditions [56], we observed an increase in Adam17 substrates in rod photoreceptor cells in OIR mice (Fig.…”
Section: Discussionmentioning
confidence: 97%
“…Both iRhoms are widely expressed, with two notable exceptions: iRhom1 expression is low or absent in myeloid cells, and iRhom2 expression is low or absent in the brain in mice, except for microglia [ 5 , 12 ]. ADAM17 has important roles in development and disease by regulating the TNFα-, EGFR- and other signaling pathways [ 12 , 13 , 14 , 15 , 16 , 17 ]. Since iRhom2 is required for the activity of ADAM17 in myeloid cells, mice lacking iRhom2 are protected from endotoxin shock and inflammatory arthritis [ 1 , 12 ], like mice lacking ADAM17 in myeloid cells [ 12 ].…”
Section: Introductionmentioning
confidence: 99%