Cloning and characterization of two alternatively spliced rat α-amidating enzyme cDNAs from rat medullary thyroid carcinoma

1990 ◽  
Vol 279 (1) ◽  
pp. 87-96 ◽  
Author(s):  
Arthur H. Bertelsen ◽  
Gary A. Beaudry ◽  
Elizabeth A. Galella ◽  
Barry N. Jones ◽  
Martha L. Ray ◽  
...  
Author(s):  
Oskar Koperek ◽  
Christian Scheuba ◽  
Christina Puri ◽  
Peter Birner ◽  
Christian Haslinger ◽  
...  

2021 ◽  
Vol 22 (19) ◽  
pp. 10463
Author(s):  
Karin Säljö ◽  
Anders Thornell ◽  
Chunsheng Jin ◽  
Olov Norlén ◽  
Susann Teneberg

Medullary thyroid carcinoma (MTC) accounts for only 1–2% of thyroid cancers; however, metastatic MTC is a mortal disease with no cure. In this study, glycosphingolipids were isolated from human MTCs and characterized by mass spectrometry and binding of carbohydrate recognizing ligands. The tissue distribution of selected compounds was investigated by immunohistochemistry. The amount of acid glycosphingolipids in the MTCs was higher than in the normal thyroid glands. The major acid glycosphingolipid was the GD3 ganglioside. Sulfatide and the gangliosides GM3 and GD1a were also present. The majority of the complex non-acid glycosphingolipids had type 2 (Galβ4GlcNAc) core chains, i.e., the neolactotetraosylceramide, the Lex, H type 2 and x2 pentaosylceramides, the Ley and A type 2 hexaosylceramides, and the A type 2 heptaosylceramide. There were also compounds with globo (GalαGalβ4Glc) core, i.e., globotriaosylceramide, globotetraosylceramide, the Forssman pentaosylceramide, and the Globo H hexaosylceramide. Immunohistochemistry demonstrated an extensive expression av Ley in the MTC cells and also a variable intensity and prevalence of Globo H and Lex. One individual with multiple endocrine neoplasia type 2B expressed the Forssman determinant, which is rarely found in humans. This study of human MTC glycosphingolipids identifies glycans that could serve as potential tumor-specific markers.


1988 ◽  
Vol 118 (1) ◽  
pp. 155-159 ◽  
Author(s):  
J. M. Conlon ◽  
L. Grimelius ◽  
G. Wallin ◽  
L. Thim

ABSTRACT An extract of a tumour metastases from a human medullary thyroid carcinoma contained a high concentration (at least 2·9 nmol/g wet weight) of the immunoregulatory peptide, thymosin-β4. The peptide was isolated as a mixture of two components with free and blocked NH2-terminal amino acid residues, the latter form predominating (approximately 98% of the total). The primary structure of the peptide was established by automated Edman degradation after cleavage with cyanogen bromide. The amino acid sequence of human thymosin-β4 was identical to thymosin-β4 previously isolated from calf thymus. Further studies are warranted to determine whether thymosin-β4 production is a useful marker for thyroid and other tumours. J. Endocr. (1988) 118, 155–159


1988 ◽  
Vol 256 (1) ◽  
pp. 245-250 ◽  
Author(s):  
J M Conlon ◽  
L Grimelius ◽  
L Thim

Four peptides derived from procalcitonin were isolated in high yield from an extract of a human medullary thyroid carcinoma. The peptides were identified as procalcitonin-(1-57)-peptide, procalcitonin-(60-91)-peptide (calcitonin), procalcitonin-(60-116)-peptide and procalcitonin-(96-116)-peptide (katacalcin). Determination of the amino acid sequence of procalcitonin-(1-57)-peptide has demonstrated that the Ala25-Ala26 bond in preprocalcitonin is the site of cleavage of the signal peptide. Procalcitonin-(60-116)-peptide represents calcitonin extended from its C-terminus by the sequence Gly-Lys-Lys-Arg-katacalcin, and its formation is indicative of an aberrant pathway of procalcitonin processing in the tumour cells.


2019 ◽  
Vol 55 (7) ◽  
pp. 559-566
Author(s):  
Kumiko Okano ◽  
Yosuke Uematsu ◽  
Kazumi Nibe ◽  
Masao Yamashita ◽  
Satoshi Suzuki ◽  
...  

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