The Aurora kinases are involved in the regulation of cell cycle progression and alterations in their expression have been shown to associate with cell malignant transformation. In the present study we demonstrated that human thyrocytes express all three Aurora kinases (A, B and C) at both protein and mRNA level and this expression is cell cycle-regulated. An increase in the protein level of the three kinases was found, with respect to normal human thyrocytes (HTU5), in the human cell lines derived from follicular (FTC-133), papillary (B-CPAP) and anaplastic (8305C) thyroid carcinomas, but not in cells derived from a follicular adenoma (HTU42). These observations were mirrored in RT-PCR experiments for Aurora-A and B. In contrast, Aurora-C mRNA levels were not significantly different among the different cell types analyzed, suggesting that post-transcriptional mechanism(s) modulate its expression. The expression at the protein level of all three Aurora kinases was significantly higher in 3 thyroid papillary carcinomas with respect to normal matched tissues obtained from the same patients. Similar modifications, at the mRNA level, could be observed in 7 papillary carcinoma tissues for Aurora-A and B, but not for Aurora-C. In conclusion, we demonstrated that normal human thyrocytes express all three members of the Aurora kinase family and their expression is amplified in malignant thyroid cell lines and tissues. These results suggest that the Aurora kinases may play a relevant role in malignant thyroid cancers, and may represent a putative therapeutic target for thyroid neoplasms.

EXPRESSION OF AURORA KINASES IN HUMAN THYROID CARCINOMA CELL LINES AND TISSUES / Ulisse, Salvatore; Delcros J., G; Baldini, Enke; Toller, M.; Curcio, F.; Giacomelli, Laura; Ambesi Impiombato, F. S.; Arlot Bonnemains, Y.; D'Armiento, Massimino. - STAMPA. - (2006), pp. 26-26. ((Intervento presentato al convegno 31st Annual Meeting of the European Thyroid Association tenutosi a NAPOLI, Italia nel 2-6 SETTEMBRE 2006.

EXPRESSION OF AURORA KINASES IN HUMAN THYROID CARCINOMA CELL LINES AND TISSUES

ULISSE, SALVATORE;BALDINI, ENKE;GIACOMELLI, Laura;D'ARMIENTO, Massimino
2006

Abstract

The Aurora kinases are involved in the regulation of cell cycle progression and alterations in their expression have been shown to associate with cell malignant transformation. In the present study we demonstrated that human thyrocytes express all three Aurora kinases (A, B and C) at both protein and mRNA level and this expression is cell cycle-regulated. An increase in the protein level of the three kinases was found, with respect to normal human thyrocytes (HTU5), in the human cell lines derived from follicular (FTC-133), papillary (B-CPAP) and anaplastic (8305C) thyroid carcinomas, but not in cells derived from a follicular adenoma (HTU42). These observations were mirrored in RT-PCR experiments for Aurora-A and B. In contrast, Aurora-C mRNA levels were not significantly different among the different cell types analyzed, suggesting that post-transcriptional mechanism(s) modulate its expression. The expression at the protein level of all three Aurora kinases was significantly higher in 3 thyroid papillary carcinomas with respect to normal matched tissues obtained from the same patients. Similar modifications, at the mRNA level, could be observed in 7 papillary carcinoma tissues for Aurora-A and B, but not for Aurora-C. In conclusion, we demonstrated that normal human thyrocytes express all three members of the Aurora kinase family and their expression is amplified in malignant thyroid cell lines and tissues. These results suggest that the Aurora kinases may play a relevant role in malignant thyroid cancers, and may represent a putative therapeutic target for thyroid neoplasms.
File allegati a questo prodotto
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/11573/419163
 Attenzione

Attenzione! I dati visualizzati non sono stati sottoposti a validazione da parte dell'ateneo

Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus ND
  • ???jsp.display-item.citation.isi??? ND
social impact