H Weiber1, Kurt Borch2, F. Sundler3, Per Fernlund4
1Surgery and
2Department of Cell Biology and Surgery, University Hospital, Linköping, and
3Department of Physiology and Neuroscience, University of Lund, Malmö, Sweden
4Clinical Chemistry, Lund University, University Hospital, Malmö
Tóm tắt
Gastric carcinoid disease may have a highly varying clinical course depending on the malignancy of the tumour. Many biochemical markers, such as peptides and biogenic amines, have been found in carcinoid tumour tissue but none has been reported to be useful as a predictor of the degree of malignancy of the carcinoid. β-Microseminoprotein is a small disulphide-rich protein with unknown function present in the secretions on most mucosal surfaces in the body, including the stomach where it is also found in some endocrine cells. We have studied β-microseminoprotein by immunohistochemistry in the tumour tissue of 29 patients with gastric carcinoid disease. β-Microseminoprotein was present in the tumour tissue in 62% of the patients and its presence was correlated to tumour diameter and tissue invasion depth. The presence of β-microseminoprotein in tumour tissue was corroborated by in situ hybridisation. All 4 patients with the solitary sporadic type of tumour and all 6 patients with metastasis had positive immunostaining of the tumour tissue. The serum concentration of β-microseminoprotein, measured by radioimmunoassay, was increased in all but 2 of 13 patients with gastric carcinoid disease. To a large part the increase was due to the concomitant atrophic corpus gastritis. We conclude that β-microseminoprotein in tumour tissue is a marker of tumour progression and that measurement of β-microseminoprotein in serum is less informative than immunohistochemistry.
