Endometrial argyrophil cell adenocarcinoma with indole- or catecholamine precursor uptake and decarboxylation.

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Biochemical and fluorescence analyses of endometrial argyrophil cell adenocarcinoma demonstrate that these tumors uptake indole and catecholamine precursors to produce serotonin and dopamine via decarboxylation.

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This study investigated the capacity of endometrial argyrophil cell adenocarcinoma to uptake and decarboxylate indole or catecholamine precursors using fluorescence microscopy, microspectrofluorometry, and biochemical analyses. Researchers examined tumors grown in nude mice and found that exposure to L-dopa and 5-hydroxytryptophan resulted in distinct fluorescent products within the cytoplasm of argyrophil cells. These findings indicated that the tumor cells produced dopamine and serotonin through the decarboxylation of their respective amine precursors. This paper is centrally about a rare malignant tumor of the endometrium, which is anatomically related to but distinct from endometriosis and adenomyosis.

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Abstract

The capacity for indole- or catecholamine precursor uptake and decarboxylation of the argyrophil cell adenocarcinoma of the endometrium was examined by fluorescence microscopy, microspectrofluorometry, and biochemical analyses. Both argyrophil and nonargyrophil cell adenocarcinomas of the human endometrium have been grown serially in nude mice. With the use of the formaldehyde-induced wet-histofluorescence method, yellowish green fluorescence was demonstrated in the cytoplasm of some cells of the argyrophil cell adenocarcinomas after exposure in vitro and in vivo to L-dopa. When 5-hydroxytrytophan was administered in vitro and in vivo to these tumors, an intense yellow fluorescence was also obtained in the cytoplasm. These fluorescent products were located in the argyrophil cells and corresponded to argyrophil granules. Microspectrofluorometrical and biochemical analyses strongly suggested that the yellowish green fluorescent products were dopamine and the yellow ones were serotonin, produced by decarboxylation of each amine precursor.
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Endometrial Argyrophil Cell Adenocarcinoma with Indole- or Catecholamine Precursor Uptake and Decarboxylation - Masaki Inoue - Gaiko Ueda - Masato Yamasaki - Keizo Hiramatsu - Yoshiaki Tanaka - Keiichi Kurachi - Kazutaka Maeyama - Atsushi Yamatodani Summary The capacity for indole- or catecholamine precursor uptake and decarboxylation of the argyrophil cell adenocarcinoma of the endometrium was examined by fluorescence microscopy, microspectrofluorometry, and biochemical analyses. Both argyrophil and nonargyrophil cell adenocarcinomas of the human endometrium have been grown serially in nude mice. With the use of the formaldehyde-induced wet-histofluorescence method, yellowish green fluorescence was demonstrated in the cytoplasm of some cells of the argyrophil cell adenocarcinomas after exposure in vitro and in vivo to L-dopa. When 5-hydroxytrytophan was administered in vitro and in vivo to these tumors, an intense yellow fluorescence was also obtained in the cytoplasm. These fluorescent products were located in the argyrophil cells and corresponded to argyrophil granules. Microspectrofluorometrical and biochemical analyses strongly suggested that the yellowish green fluorescent products were dopamine and the yellow ones were serotonin, produced by decarboxylation of each amine precursor.

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