Gastrin stimulates a cholecystokinin-2-receptor-expressing cardia progenitor cell and promotes progression of Barrett's-like esophagus
| العنوان: | Gastrin stimulates a cholecystokinin-2-receptor-expressing cardia progenitor cell and promotes progression of Barrett's-like esophagus |
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| المؤلفون: | Malcolm Boyce, Julian A. Abrams, Yoku Hayakawa, Govind Bhagat, Wenju Chang, Andrew S. Au, Hongshan Wang, Kenneth K. Wang, Richard A. Friedman, Aleksandra M. Urbanska, Aesis M. Luna, Timothy C. Wang, Anil K. Rustgi, Guangchun Jin, Yoomi Lee, Andrea Varro, Michael Quante, Antonia R. Sepulveda |
| المصدر: | Oncotarget ONCOTARGET |
| بيانات النشر: | Impact Journals, LLC, 2016. |
| سنة النشر: | 2016 |
| مصطلحات موضوعية: | 0301 basic medicine, Oncology, endocrine system, medicine.medical_specialty, Pathology, Mice, Transgenic, digestive system, Barrett's esophagus, Barrett Esophagus, Mice, 03 medical and health sciences, 0302 clinical medicine, stem cells, Internal medicine, Metaplasia, gastrin, Gastrins, medicine, Animals, esophageal cancer, Esophagus, Gastrin, business.industry, Cancer, Hepatology, Esophageal cancer, medicine.disease, Immunohistochemistry, digestive system diseases, Receptor, Cholecystokinin B, 3. Good health, Disease Models, Animal, gastrin receptors, Phenotype, 030104 developmental biology, medicine.anatomical_structure, Gene Expression Regulation, Dysplasia, Hyperglycemia, Disease Progression, 030211 gastroenterology & hepatology, medicine.symptom, business, Biomarkers, Myoblasts, Cardiac, Research Paper |
| الوصف: | // Yoomi Lee 1, * , Aleksandra M. Urbanska 2, * , Yoku Hayakawa 2 , Hongshan Wang 2, 3 , Andrew S. Au 2 , Aesis M. Luna 4 , Wenju Chang 2, 3 , Guangchun Jin 2 , Govind Bhagat 4 , Julian A. Abrams 2 , Richard A. Friedman 5, 6 , Andrea Varro 7 , Kenneth K. Wang 8 , Malcolm Boyce 9 , Anil K. Rustgi 10 , Antonia R. Sepulveda 4 , Michael Quante 11 , Timothy C. Wang 2 1 Division of Hematology and Oncology, Department of Medicine, Columbia University Medical Center, New York, NY, USA 2 Division of Digestive and Liver Diseases, Department of Medicine, Columbia University Medical Center, New York, NY, USA 3 Department of General Surgery, Zhongshan Hospital, Fudan University, Shanghai, China 4 Department of Pathology and Cell Biology, Columbia University Medical Center, New York, NY, USA 5 Biomedical Informatics Shared Resource, Herbert Irving Comprehensive Cancer Center, New York, NY, USA 6 Department of Biomedical Informatics, Columbia University Medical Center, New York, NY, USA 7 Department of Physiology, Institute of Translational Medicine, University of Liverpool, Liverpool, England 8 Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, USA 9 Hammersmith Medicines Research, Central Middlesex Hospital, London, UK 10 Division of Gastroenterology, Departments of Medicine and Genetics, Abramson Cancer Center, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA 11 Medical Clinic II, Clinic of the Right Bank, Technical University of Munich, Munich, Germany * These authors contributed equally to this work Correspondence to: Timothy C. Wang, email: tcw21@columbia.edu Keywords: Barrett’s esophagus, esophageal cancer, gastrin, gastrin receptors, stem cells Received: March 15, 2016 Accepted: June 13, 2016 Published: July 18, 2016 ABSTRACT Objective: The incidence of esophageal adenocarcinoma (EAC) is increasing, but factors contributing to malignant progression of its precursor lesion, Barrett’s esophagus (BE), have not been defined. Hypergastrinemia caused by long-term use of proton pump inhibitors (PPIs), has been suggested as one possible risk factor. The gastrin receptor, CCK2R, is expressed in the cardia and upregulated in BE, suggesting the involvement of the gastrin-CCK2R pathway in progression. In the L2-IL-1β mouse model, Barrett’s-like esophagus arises from the gastric cardia. Therefore, we aimed to analyze the effect of hypergastrinemia on CCK2R+ progenitor cells in L2-IL-1β mice. Design: L2-IL-1β mice were mated with hypergastrinemic ( INS-GAS ) mice or treated with PPIs to examine the effect of hypergastrinemia in BE progression. CCK2R-CreERT crossed with L2-IL-1β mice were used to analyze the lineage progenitor potential of CCK2R+ cells. Cardia glands were cultured in vitro , and the effect of gastrin treatment analyzed. L2-IL-1β mice were treated with a CCK2R antagonist YF476 as a potential chemopreventive drug. Results: Hypergastrinemia resulted in increased proliferation and expansion of Barrett’s-like esophagus. Lineage tracing experiments revealed that CCK2R+ cells are long-lived progenitors that can give rise to such lesions under chronic inflammation. Gastrin stimulated organoid growth in cardia culture, while CCK2R inhibition prevented Barrett’s-like esophagus and dysplasia. Conclusions: Our data suggest a progression model for BE to EAC in which CCK2R+ progenitor cells, stimulated by hypergastrinemia, proliferate to give rise to metaplasia and dysplasia. Hypergastrinemia can result from PPI use, and the effects of hypergastrinemia in human BE should be studied further. |
| وصف الملف: | application/pdf |
| تدمد: | 1949-2553 |
| الوصول الحر: | https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1e0609e188fc739e42ec38037afe2f6Test https://doi.org/10.18632/oncotarget.10667Test |
| حقوق: | OPEN |
| رقم الانضمام: | edsair.doi.dedup.....f1e0609e188fc739e42ec38037afe2f6 |
| قاعدة البيانات: | OpenAIRE |
| تدمد: | 19492553 |
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