Gastrin in Non-Neoplastic Pancreatic Tissue from Patients with and without Gastrinomas

References

• Boel E, Vuust J, Norris F, et al. Molecular cloning of human gastrin cDNA, evidence for evolution of gastrin by gene duplication. Proc Natl Acad Sci USA 1983; 80: 2866–2869
   PubMed Web of Science ®Google Scholar
• Kato K, Himeno S, Takahashi Y, Wakabayashi T, Tarui S, Matsubara K. Molecular cloning of human gastrin precursor cDNA. Gene 1983; 26: 53–57
   PubMedGoogle Scholar
• Gregory R A, Tracy H J. The constitution and properties of two gastrins extracted from hog antral mucosa. Gut 1964; 5: 103–117
   PubMed Web of Science ®Google Scholar
• Rehfeld J F, Stadil F, Vikelsøe J. Immunoreactive gastrin components in human serum. Gut 1974; 15: 102–111
   PubMed Web of Science ®Google Scholar
• Dockray G J, Varro A, Desmond H, Young J, Gregory H, Gregory R A. Post-translational processing of the porcine gastrin precursor by phosphorylation of the COOH-terminal fragment. J Biol Chem 1987; 262: 8643–8647
   PubMed Web of Science ®Google Scholar
• Desmond H, Pauwels S, Varro A, Gregory H, Young J, Dockray G J. Isolation and characterization of the intact gastrin precursor from a gastrinoma. FEBS Lett 1987; 210: 185–188
   PubMed Web of Science ®Google Scholar
• Morley J S, Tracy H J, Gregory R A. Structure-function relationships in the active C-terminal tetra-peptide amide sequence of gastrin. Nature 1965; 207: 1356–1360
   PubMed Web of Science ®Google Scholar
• Bradbury A F, Finnie M DA, Smyth D G. Mechanism of C-terminal amide formation by pituitary enzymes. Nature 1982; 298: 686–688
   PubMed Web of Science ®Google Scholar
• Noe B D. Converting enzymes. Current trends in tumour pathology. Endocrine tumours. Vol. 1, J M Polak, S R Bloom. Churchill Livingstone, Edinburgh 1985; 57–81
   Google Scholar
• Rehfeld J F. Accumulation of nonamidated pre-progastrin and preprocholecystokinin products in porcine pituitary corticotrophs. Evidence of post-translational control of cell differentiation. J Biol Chem 1986; 261: 5841–5847
   PubMed Web of Science ®Google Scholar
• Rehfeld J F, Bardram L, Cantor P, Hilsted L, Schwartz T W. Cell specific processing of pro-cholecystokinin and progastrin. Biochimie 1988; 70: 25–31
   PubMedGoogle Scholar
• Bardram L, Rehfeld J F. Processing-independent radioimmunoanalysis. A general analytical principle applied to progastrin and its products. Anal Biochem 1988; 175: 537–543
   PubMed Web of Science ®Google Scholar
• Bardram L, Hilsted L, Rehfeld J F. Progastrin expression in the mammalian pancreas. Proc Natl Acad Sci USA 1990; 87: 298–302
   PubMed Web of Science ®Google Scholar
• Rehfeld J F, Stadil F, Rubin B. Production and evaluation of antibodies for the radioimmunoassay of gastrin. Scand J Clin Lab Invest 1972; 30: 221–232
   PubMed Web of Science ®Google Scholar
• Bardram L, Rehfeld J F. Production and evaluation of monospecific antibodies for a processing-independent sequence of human progastrin. Scand J Clin Lab Invest 1989; 49: 173–182
   PubMed Web of Science ®Google Scholar
• Hilsted L, Rehfeld J F. Measurement of precursors for α-amidated hormones by radioimmunoassay of glycine-extended peptides after trypsin-carboxy-peptidase B cleavage. Anal Biochem 1986; 152: 119–126
   PubMed Web of Science ®Google Scholar
• Hilsted L, Rehfeld J F. α-Amidation of antral progastrin, relation to other posttranslational modifications. J Biol (Them 1987; 262: 16953–16957
   Google Scholar
• Stadil F, Rehfeld J F. Preparation of 125I-labelled synthetic human gastrin I for radioimmunoanalysis. Scand J Clin Lab Invest 1972; 30: 361–368
   PubMed Web of Science ®Google Scholar
• Sugano K, Aponte G W, Yamada T. Identification and characterization of glycine-extended posttranslational processing intermediates of progastrin in porcine stomach. J Biol Chem 1985; 260: 11724–11729
   PubMed Web of Science ®Google Scholar
• Lotstra F, van der Loo W, Gepts W. Are gastrin cells present in mammalian pancreatic islets?. Diabetologia 1974; 10: 291–302
   PubMedGoogle Scholar
• Larsson L-I, Håkanson R, Sjöberg N-O, Sundler F. Fluorescence histochemistry of the gastrin cell in fetal and adult man. Gastroenterology 1975; 68: 1152–1159
   PubMed Web of Science ®Google Scholar
• Creutzfledt W, Arnold R, Creutzfeldt C. Track NS. Pathomorphologic, biochemical and diagnostic aspects of gastrinomas (Zollinger-Ellison syndrome). Human Pathol 1975; 6: 47–76
   PubMedGoogle Scholar
• Larsson L-I, Rehfeld J F, Goltermann N. Gastrin in the human fetus. Distribution and molecular forms of gastrin in the antro-pyloric gland area, duodenum and pancreas. Scand J Gastroenterol 1977; 12: 869–872
   PubMed Web of Science ®Google Scholar
• Larsson L-I. Two distinct types of islet abnormalities associated with endocrine pancreatic tumours. Virchows Arch [Pathol Anat] 1977; 376: 209–219
   PubMedGoogle Scholar
• Andersen B N, Abramovich D, Brand S J, Petersen B, Rehfeld J F. Complete sulfation of jejunal gastrin in the human fetus. Reg Peptides 1985; 10: 329–338
   PubMedGoogle Scholar
• Ellisom E H, Wilson D. The Zollinger-Ellison syndrome. Reappraisal and evaluation of 260 registered cases. Ann Surg 1964; 160: 512–520
   PubMedGoogle Scholar
• Larsson L-I, Rehfeld J F, Sundler F, Håkanson R. Pancreatic gastrin in neonatal rats. Nature 1976; 262: 609–610
   PubMed Web of Science ®Google Scholar
• Onolfo J P, Lehy T. Comparative development of gastrin and somatostatin cell populations in the pancreas stomach and duodenum of the rat during the perinatal period. Anat Rec 1987; 218: 416–425
   PubMedGoogle Scholar
• Fujii S. Development of pancreatic endocrine cells in the rat fetus. Arch Histol Jpn 1979; 42: 467–479
   PubMedGoogle Scholar
• Rehfeld J F, Larsson L-I, Goltermann N, et al. Neural regulation of pancreatic hormone secretion by the C-terminal treatapeptide of CCK. Nature 1980; 284: 33–38
   PubMed Web of Science ®Google Scholar
• Kelly R B. Pathways of protein secretion in eukaryotes. Science 1980; 230: 25–32
   Google Scholar
• Johnson L R. Effect of gastrointestinal hormones on growth of gastrointestinal tissue. Gastrointestinal hormones, G BJ Glass. Raven Press, New York 1980; 507–527
   Google Scholar
• Dembinsky A B, Johnson L R. Stimulation of pancreatic growth by secretin, caerulein and pentagastrin. Endocrinology 1980; 106: 323–328
   PubMed Web of Science ®Google Scholar
• Larsson L-I, Ljungberg O, Sundler F, et al. Antropyloric gastrinoma associated with pancreatic nesidioblastosis and proliferation of islets. Virchows Arch [Pathol Anat] 1973; 360: 305–314
   PubMedGoogle Scholar
• Bani Sacchi T, Bani D, Biliotti G. Nesidioblastosis and islet cell changes related to endogenous hypergastrinemia. Virchows Arch [Cell Pathol] 1986; 48: 261–276
   Google Scholar
• Hollande E, Giron B, Lehy T, Accary J P, Rozé C. In vitro secretion of gastrin, insulin and glucagon in tissue cultures of pancreas from a child with neonatal intractable hypoglycemia. Gastroenterology 1976; 71: 255–262
   PubMedGoogle Scholar
• Brand S J, Andersen B N, Rehfeld J F. Complete tyrosine-O-sulfation of gastrin in neonatal rat pancreas. Nature 1984; 309: 456–458
   PubMed Web of Science ®Google Scholar
• Brand S J, Fuller P J. Differential gastrin gene expression in rat gastrointestinal tract and pancreas during neonatal development. J Biol Chem 1988; 263: 5341–5347
   PubMed Web of Science ®Google Scholar