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Molecular and Cellular Mechanisms Underlying Gastrointestinal Diseases

A special issue of International Journal of Molecular Sciences (ISSN 1422-0067). This special issue belongs to the section "Molecular Pathology, Diagnostics, and Therapeutics".

Deadline for manuscript submissions: closed (30 April 2024) | Viewed by 903

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Guest Editor
Department of Pharmacology, School of Korean Medicine, Wonkwang University, Iksan 54538, Republic of Korea
Interests: Korean medicine; inflammation; oxidative stress; gastrointestinal diseases
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

This Research Topic aims to discover and develop novel strategies or mechanisms, single compounds, natural products or combination formulas with beneficial properties in various gastrointestinal disease models. Topics of interest include pharmacokinetics, metabolism, pharmacology, cohort studies and toxicology related to the use of drugs in gastrointestinal diseases. While experimental drug mechanisms primarily concentrate on pharmacological research of new agents, novel pharmacodynamic and pharmacokinetic mechanisms that may explain or predict the molecular and cellular mechanisms of gastrointestinal diseases already in use and/or provide potential targets for drug development may also be welcome.

In this Research Topic, we welcome original research, reviews and communications focused on these molecular and cellular mechanisms.

Dr. Gi-Sang Bae
Guest Editor

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Keywords

  • gastrointestinal diseases
  • liver
  • pancreas
  • inflammation bowel diseases
  • dyspepsia

Published Papers (1 paper)

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Research

12 pages, 1073 KiB  
Article
Neutrophil Gelatinase-Associated Lipocalin for the Differentiation of Mucinous Pancreatic Cystic Lesions
by Miruna Patricia Olar, Maria Iacobescu, Sorana D. Bolboacă, Cristina Pojoga, Ofelia Moșteanu, Radu Seicean, Ioana Rusu, Oana Banc, Cristina Adela Iuga and Andrada Seicean
Int. J. Mol. Sci. 2024, 25(6), 3224; https://doi.org/10.3390/ijms25063224 - 12 Mar 2024
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Abstract
Undetermined pancreatic cystic lesion (PCL) differentiation benefits from endoscopic ultrasound (EUS) based on morphology and cyst fluid analysis, but room for new biomarkers exists. Our aim was to assess the intracystic and serum diagnostic value of neutrophil gelatinase-associated lipocalin (Ngal) and interleukin 1 [...] Read more.
Undetermined pancreatic cystic lesion (PCL) differentiation benefits from endoscopic ultrasound (EUS) based on morphology and cyst fluid analysis, but room for new biomarkers exists. Our aim was to assess the intracystic and serum diagnostic value of neutrophil gelatinase-associated lipocalin (Ngal) and interleukin 1 beta (IL-1β) for differentiation of PCLs. This prospective study included patients from one tertiary hospital, evaluated between April 2018 and May 2020. EUS fine-needle aspiration or pancreatic pseudocysts drainage was the source of PCL intracystic liquid. The final diagnosis was based on surgery or EUS results (morphology, cytology, glucose, and CEA—carcinoembryogenic antigen). The intracystic samples were tested for Ngal, IL-1β, glucose, and CEA, and serum for Ngal and IL-1β. We evaluated 63 cysts, 33 pseudocysts, and 30 non-inflammatory cysts. The diagnostic sensitivity and specificity for mucinous PCL was 70.8% and 92.3% for intracystic Ngal (cut-off: 500–800 ng/dL), without correlation with serum Ngal, no matter the inclusion of infected pseudocysts. After exclusion of infected pseudocysts, the sensitivity and specificity for glucose were 87% and 75%, respectively, and for CEA, they were 87.1%, and 96.8%, respectively. Intracystic Ngal shows promise in differentiating mucinous PCLs, but researchers need to conduct further studies to confirm its effectiveness. Intracystic IL-1β and serum Ngal made no diagnostic contribution. Full article
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