Acinar-ductal-carcinoma sequence in transforming growth factor-α transgenic mice
被引:30
作者:
Schmid, RM
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机构:Univ Ulm, Dept Internal Med 1, D-89081 Ulm, Germany
Schmid, RM
Klöppel, G
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机构:Univ Ulm, Dept Internal Med 1, D-89081 Ulm, Germany
Klöppel, G
Adler, G
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机构:Univ Ulm, Dept Internal Med 1, D-89081 Ulm, Germany
Adler, G
Wagner, M
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h-index: 0
机构:Univ Ulm, Dept Internal Med 1, D-89081 Ulm, Germany
Wagner, M
机构:
[1] Univ Ulm, Dept Internal Med 1, D-89081 Ulm, Germany
[2] Univ Kiel, Dept Pathol, D-24105 Kiel, Germany
来源:
CELL AND MOLECULAR BIOLOGY OF PANCREATIC CARCINOMA: RECENT DEVELOPMENTS IN RESEARCH AND EXPERIMENTAL THERAPY
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1999年
/
880卷
关键词:
D O I:
10.1111/j.1749-6632.1999.tb09526.x
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Transgenic mice overexpressing transforming growth factor-alpha (TGF-alpha) display an expansion of intrapancreatic fibroblasts and a progressive accumulation of extracellular;matrix, This massive fibrosis is associated with an increase in pancreatic size and weight. In parallel, tubular complexes appear that are composed of acinar cells with a decreased height. These acinar cells lose zymogen granules and become transitional cells, which subsequently gain duct cell features. In animals older than one year dysplastic lesions develop, which originate from tubular complexes. Occasionally these dysplastic foci transform to papillary and cystic pancreatic carcinoma. These tumors are positive for the duct-specific antigen Duct-1 and carbonic anhydrase activity indicative of ductal differentiation. Tumors overexpress the epidermal growth factor (EGF)-receptor and p53, but lack K-ras mutations. These data suggest an acinar-ductal-carcinoma sequence in TGF-alpha transgenic mice.