دورية أكاديمية
أعرض في EDS

Murine Models of Gastric Corpus Preneoplasia.

التفاصيل البيبلوغرافية
العنوان: Murine Models of Gastric Corpus Preneoplasia.
المؤلفون: Petersen CP; Nashville VA Medical Center, Nashville, Tennessee; Department of Cell and Developmental Biology, Vanderbilt University, Nashville, Tennessee; Epithelial Biology Center, Vanderbilt University, Nashville, Tennessee., Mills JC; Division of Gastroenterology, Department of Medicine, Pathology and Immunology, Department of Developmental Biology, Washington University School of Medicine, St. Louis, Missouri., Goldenring JR; Nashville VA Medical Center, Nashville, Tennessee; Section of Surgical Sciences, Vanderbilt University, Nashville, Tennessee; Department of Cell and Developmental Biology, Vanderbilt University, Nashville, Tennessee; Epithelial Biology Center, Vanderbilt University, Nashville, Tennessee.
المصدر: Cellular and molecular gastroenterology and hepatology [Cell Mol Gastroenterol Hepatol] 2016 Nov 16; Vol. 3 (1), pp. 11-26. Date of Electronic Publication: 2016 Nov 16 (Print Publication: 2017).
نوع المنشور: Journal Article; Review
اللغة: English
بيانات الدورية: Publisher: American Gastroenterological Association Country of Publication: United States NLM ID: 101648302 Publication Model: eCollection Cited Medium: Print ISSN: 2352-345X (Print) Linking ISSN: 2352345X NLM ISO Abbreviation: Cell Mol Gastroenterol Hepatol Subsets: PubMed not MEDLINE
أسماء مطبوعة: Original Publication: Philadelphia, PA : American Gastroenterological Association, [2015]-
مستخلص: Intestinal-type gastric adenocarcinoma evolves in a field of pre-existing metaplasia. Over the past 20 years, a number of murine models have been developed to address aspects of the physiology and pathophysiology of metaplasia induction. Although none of these models has achieved true recapitulation of the induction of adenocarcinoma, they have led to important insights into the factors that influence the induction and progression of metaplasia. Here, we review the pathologic definitions relevant to alterations in gastric corpus lineages and classification of metaplasia by specific lineage markers. In addition, we review present murine models of the induction and progression of spasmolytic polypeptide (TFF2)-expressing metaplasia, the predominant metaplastic lineage observed in murine models. These models provide a basis for the development of a broader understanding of the physiological and pathophysiological roles of metaplasia in the stomach.
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معلومات مُعتمدة: R01 DK094989 United States DK NIDDK NIH HHS; R01 DK071590 United States DK NIDDK NIH HHS; R01 DK101332 United States DK NIDDK NIH HHS; F31 DK104600 United States DK NIDDK NIH HHS; I01 BX000930 United States BX BLRD VA; P30 DK052574 United States DK NIDDK NIH HHS; R01 DK105129 United States DK NIDDK NIH HHS
فهرسة مساهمة: Keywords: ATPase, adenosine triphosphatase; BMP, bone morphogenic protein; Chief Cell; EGF, epidermal growth factor; EGFR, epidermal growth factor receptor; Gastric Cancer; Hip1r, Huntington interacting protein 1 related; Hyperplasia; IFN, interferon; Intestinal Metaplasia; MUC, mucin; SDF1, stromal-derived factor 1; SPEM; SPEM, spasmolytic polypeptide–expressing metaplasia; TFF, trefoil factor; TFF2; TGF, transforming growth factor; Tg, transgene; Th, T-helper
تواريخ الأحداث: Date Created: 20170209 Latest Revision: 20220318
رمز التحديث: 20240628
مُعرف محوري في PubMed: PMC5247421
DOI: 10.1016/j.jcmgh.2016.11.001
PMID: 28174755
قاعدة البيانات: MEDLINE
الوصف
تدمد:2352-345X
DOI:10.1016/j.jcmgh.2016.11.001