Acinar-ductal-carcinoma sequence in transforming growth factor-α transgenic mice

被引:30
作者
Schmid, RM
Klöppel, G
Adler, G
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 | 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.
引用
收藏
页码:219 / 230
页数:12
相关论文
共 41 条
  • [1] MOST HUMAN CARCINOMAS OF THE EXOCRINE PANCREAS CONTAIN MUTANT C-K-RAS GENES
    ALMOGUERA, C
    SHIBATA, D
    FORRESTER, K
    MARTIN, J
    ARNHEIM, N
    PERUCHO, M
    [J]. CELL, 1988, 53 (04) : 549 - 554
  • [2] BARTON CM, 1991, J PATHOL, V163, P111, DOI 10.1002/path.1711630206
  • [3] ABNORMALITIES OF THE P53 TUMOR SUPPRESSOR GENE IN HUMAN PANCREATIC-CANCER
    BARTON, CM
    STADDON, SL
    HUGHES, CM
    HALL, PA
    OSULLIVAN, C
    KLOPPEL, G
    THEIS, B
    RUSSELL, RCG
    NEOPTOLEMOS, J
    WILLIAMSON, RCN
    LANE, DP
    LEMOINE, NR
    [J]. BRITISH JOURNAL OF CANCER, 1991, 64 (06) : 1076 - 1082
  • [4] CYTOLOGICAL CHANGES IN THE PANCREAS OF TRANSGENIC MICE OVEREXPRESSING TRANSFORMING GROWTH-FACTOR ALPHA
    BOCKMAN, DE
    MERLINO, G
    [J]. GASTROENTEROLOGY, 1992, 103 (06) : 1883 - 1892
  • [5] DISCORDANCE OF EXOCRINE AND ENDOCRINE GROWTH AFTER 90-PERCENT PANCREATECTOMY IN RATS
    BROCKENBROUGH, JS
    WEIR, GC
    BONNERWEIR, S
    [J]. DIABETES, 1988, 37 (02) : 232 - 236
  • [6] FREQUENT SOMATIC MUTATIONS AND HOMOZYGOUS DELETIONS OF THE P16 (MTS1) GENE IN PANCREATIC ADENOCARCINOMA
    CALDAS, C
    HAHN, SA
    DACOSTA, LT
    REDSTON, MS
    SCHUTTE, M
    SEYMOUR, AB
    WEINSTEIN, CL
    HRUBAN, RH
    YEO, CJ
    KERN, SE
    [J]. NATURE GENETICS, 1994, 8 (01) : 27 - 32
  • [7] CERY WL, 1990, CARCINOGENESIS, V11, P2075
  • [8] CUBILLA AL, 1975, CANCER RES, V35, P2234
  • [9] DELISLE RC, 1990, EUR J CELL BIOL, V51, P64
  • [10] INDUCTION OF ISLET CYTODIFFERENTIATION BY FETAL MESENCHYME IN ADULT PANCREATIC DUCTAL EPITHELIUM
    DUDEK, RW
    LAWRENCE, IE
    HILL, RS
    JOHNSON, RC
    [J]. DIABETES, 1991, 40 (08) : 1041 - 1048