Carboxylic Ester Hydrolase and Amylase in Ischemic Pancreatitis in the Guinea Pig

Pj, Blind; Bläckberg, Lars; Eb, Lundström; Emdin, SO; Hernell, Olle

doi:10.1097/00006676-199605000-00011

Cited by 3 publications

(1 citation statement)

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“…Indeed, serum levels of BSDL are significantly increased in patients suffering from acute interstitial pancreatitis or necrotizing pancreatitis [ 110 ]. A high serum level of BSDL, therefore, even where serum levels of amylase are normal [ 124 ], suggests acute pancreatitis [ 125 ].…”

Section: Introductionmentioning

confidence: 99%

Pancreatic adenocarcinoma, chronic pancreatitis, and MODY-8 diabetes: is bile salt-dependent lipase (or carboxyl ester lipase) at the crossroads of pancreatic pathologies?

et al. 2017

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Pancreatic adenocarcinomas and diabetes mellitus are responsible for the deaths of around two million people each year worldwide. Patients with chronic pancreatitis do not die directly of this disease, except where the pathology is hereditary. Much current literature supports the involvement of bile salt-dependent lipase (BSDL), also known as carboxyl ester lipase (CEL), in the pathophysiology of these pancreatic diseases. The purpose of this review is to shed light on connections between chronic pancreatitis, diabetes, and pancreatic adenocarcinomas by gaining an insight into BSDL and its variants. This enzyme is normally secreted by the exocrine pancreas, and is diverted within the intestinal lumen to participate in the hydrolysis of dietary lipids. However, BSDL is also expressed by other cells and tissues, where it participates in lipid homeostasis. Variants of BSDL resulting from germline and/or somatic mutations (nucleotide insertion/deletion or nonallelic homologous recombination) are expressed in the pancreas of patients with pancreatic pathologies such as chronic pancreatitis, MODY-8, and pancreatic adenocarcinomas. We discuss the possible link between the expression of BSDL variants and these dramatic pancreatic pathologies, putting forward the suggestion that BSDL and its variants are implicated in the cell lipid metabolism/reprogramming that leads to the dyslipidemia observed in chronic pancreatitis, MODY-8, and pancreatic adenocarcinomas. We also propose potential strategies for translation to therapeutic applications.

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Section: Introductionmentioning

confidence: 99%