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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 65 (1987), S. 82-86 
    ISSN: 1432-1440
    Keywords: Katacalcin ; Tumor marker ; C-cell carcinoma
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Katacalcin (KC) is situated on the C-terminal side of the procalcitonin molecule and is cleaved like calcitonin (CT) from this precursor peptide. Serum levels of KC were measured in 22 patients with C-cell carcinoma with a specific and sensitive radioimmunoassay (normal range, 〈0.1–0.15 ng/ml). Basal serum KC values in C-cell carcinoma patients were 0.32-290 ng/ml. There was a good correlation between KC and CT (r=0.98,P〈0.001). Serum KC, as well as CT, markedly increased after pentagastrin and calcium infusion. KC and CT were secreted in nearly equimolar amounts. During selective venous catheterization, KC and CT levels were increased in serum samples from veins draining tumor masses, which could be confirmed operatively. During the follow up, KC and CT measurements correlated well to the stage of disease. KC could be immunohistologically localized in C-cell carcinoma tissue. As a tumor marker, katacalcin is likely to be as useful as calcitonin in C-cell carcinoma.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 56 (1978), S. 697-701 
    ISSN: 1432-1440
    Keywords: Calcitonin ; Phäochromocytom ; Sipple-Syndrom ; Tumor „Marker“ ; Paraneoplastische Hormonsekretion ; Calcitonin ; Pheochromocytoma ; Sipple-syndrome ; Tumor marker ; Paraneoplastic hormone secretion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Summary As pheochromocytoma sometimes is accompanied by medullary thyroid carcinoma (in the sense of multiple endocrine adonomatosis type II=Sipple-Syndrome), serum calcitonin (CT) was measured by radioimmunoassay in 4 patients with pheochromocytoma. Before extirpation of the adreno-medullary tumor, serum CT was distinctly increased to 3 and 30 ng/ml in 2 of 4 patients, respectively. After removal of the tumor, serum CT was normal in the patients and pentagastrin stimulation produced no exaggerated CT response. In hydrochloric acid extracts from the two corresponding pheochromocytoma tissues, immunoreactive-Calcitonin (IR-CT) was detected, the concentrations amounting 1 and 4 ng/mg wet tissue. These findings suggest that hypercalcitonism in patients with pheochromocytoma cannot always be ascribed to the thyroid, i.e. increased calcitonin levels do not necessarily indicate a medullary carcinoma of this organ.
    Notes: Zusammenfassung Da Phäochromocytome in Kombination mit einem medullären Schilddrüsen-Carzinom auftreten können (multiple endokrine Adenomatose Typ II=Sipple-Syndrom), wurden bei 4 Patienten mit Phäochromocytomen die Serumcalcitoninspiegel radioimmunologisch bestimmt. Bei 2 der 4 Patienten fanden sich vor Operation des Nebennierenmarktumors deutlich erhöhte Calcitoninspiegel von 3 und 30 ng/ml. Nach Entfernung des Tumors normalisierten sich die Calcitoninspiegel, ebenso erzeugte die Pentagastrin-Stimulation keinen pathologischen Anstieg des Calcitonins. In salzsauren Extrakten aus den entsprechenden beiden Phäochromocytomen fand sich radioimmunologisch bestimmbares Calcitonin; die Werte betrugen 1und 4 ng/mg Frischgewicht. Der Nachweis einer Hypercalcitoninämie bei Patienten mit Phäochromocytomen läßt daher nicht unbedingt den Schluß auf ein gleichzeitig bestehendes medulläres Schilddrüsen-Carcinom zu, da offensichtlich Nebennierenmarktumoren zu Calcitoninproduktion und -sekretion fähig sind.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-1335
    Keywords: Neuron-specific enolase ; Medullary thyroid carcinoma ; Tumor marker ; Calcitonin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Neuron-specific enolase (NSE) is an enzyme detectable in nervous and neuroendocrine tissue. Increased serum levels of NSE are found in small cell lung cancer and in patients with neuroblastoma, in whom NSE is used as a serum tumor marker. We have investigated 32 patients with histologically proven medullary thyroid carcinoma, a tumor of neuroendocrine origin, in which the classical tumor marker calcitonin (CT) was pathologically elevated. Positive immunocytochemistry for NSE and CT in C-cells was obtained in all cases. Increased serum NSE levels were found in only 5 of 32 patients, there was no correlation between NSE and CT concentrations. We also compared NSE and CT serum levels during long-term follow-up and again found no correlation between NSE and CT. After i.v. stimulation tests with pentagastrin and calcium, no correlation was found between NSE and CT serum levels. We conclude, therefore, that in medullary thyroid carcinoma NSE is useful for immunocytochemistry but not a reliable serum tumor marker.
    Type of Medium: Electronic Resource
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