2017
DOI: 10.1016/s0016-5085(17)33061-5
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Extracellular ATP Promotes Systemic Inflammation During Acute Pancreatitis

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Cited by 2 publications
(5 citation statements)
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“…While assessing the carcinoma tissue samples, the average expression values of P2X4 and P2X7 increased vigorously, this aligns with the recent evidence to strengthen the theory of P2X4 and P2X7 receptors' association with incessant inflammation. A relatively gradual increase in their expression with the development of disease has been found substantial in multiple cancer types [14,25,28,29]. The P2X4 and P2X7 receptors' expression for a specific cancer type in the studied carcinomas was relatively equal with a nominal difference which is affirmed by a recent evidence of P2X4 and P2X7 receptors' co-expression in the form of hetero-trimers on the cell surface [30][31][32].…”
Section: Comparative Analysis Of P2x4 and P2x7 In Hepatocellular Carcsupporting
confidence: 56%
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“…While assessing the carcinoma tissue samples, the average expression values of P2X4 and P2X7 increased vigorously, this aligns with the recent evidence to strengthen the theory of P2X4 and P2X7 receptors' association with incessant inflammation. A relatively gradual increase in their expression with the development of disease has been found substantial in multiple cancer types [14,25,28,29]. The P2X4 and P2X7 receptors' expression for a specific cancer type in the studied carcinomas was relatively equal with a nominal difference which is affirmed by a recent evidence of P2X4 and P2X7 receptors' co-expression in the form of hetero-trimers on the cell surface [30][31][32].…”
Section: Comparative Analysis Of P2x4 and P2x7 In Hepatocellular Carcsupporting
confidence: 56%
“…Recently, purinergic signaling has emerged as an essential signaling mechanism to regulate inflammation [14]. Two key receptors in purinergic signaling are P2X4 and P2X7.…”
Section: Introductionmentioning
confidence: 99%
“…Given that ATP mainly kept in reserve at acinar cells with high concentration, the elevating extracellular concentration of ATP is thought to attribute to the release of injured cells (Yegutkin et al, 2006). Necrotic Acinar cells undergoing cytoplasmic membrane destruction are likely to be the main source of extracellular ATP (eATP) (Dixit et al, 2019b). Other sources of high eATP levels may include activated immune cells, duct cells, endothelial cells, or even cells undergoing apoptosis (Bodin and Burnstock, 1996;Elliott et al, 2009;Junger, 2011;Kowal et al, 2015).…”
Section: Atp and Apmentioning
confidence: 99%
“…Hence, this interaction enhances cell damage. Nevertheless, there still could be an abundant amount of ATP, which, if released, can play an essential role as DAMPs by activating purinergic signaling (Dixit et al, 2019b).…”
Section: Atp and Apmentioning
confidence: 99%
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