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The neutrophil gelatinase-associated lipocalin (NGAL), a NF-[kappa]B-regulated gene, is a survival factor for thyroid neoplastic cells

Authors :
Iannetti, Alessio
Pacifico, Francesco
Acquaviva, Renato
Lavorgna, Alfonso
Crescenzi, Elvira
Vascotto, Carlo
Tell, Gianluca
Salzano, Anna Maria
Scaloni, Andrea
Vuttariello, Emilia
Chiappetta, Gennaro
Leonardi, Silvestro Formisano Antonio
Source :
Proceedings of the National Academy of Sciences of the United States. Sept 16, 2008, Vol. 105 Issue 37, p14058, 6 p.
Publication Year :
2008

Abstract

NF-[kappa]B is constitutively activated in primary human thyroid tumors, particularly in those of anaplastic type. The inhibition of NF-[kappa]B activity in the human anaplastic thyroid carcinoma cell line, FRO, leads to an increased susceptibility to chemotherapeutic drug-induced apoptosis and to the blockage of their ability to form tumors in nude mice. To identify NF-[kappa]B target genes involved in thyroid cancer, we analyzed the secretome of conditioned media from parental and NF-[kappa]B-null FRO cells. Proteomic analysis revealed that the neutrophil gelatinase-associated lipocalin (NGAL), a protein involved in inflammatory and immune responses, is secreted by FRO cells whereas its expression is strongly reduced in the NF-[kappa]B-null FRO cells. NGAL is highly expressed in human thyroid carcinomas, and knocking down its expression blocks the ability of FRO cells to grow in soft agar and form tumors in nude mice. These effects are reverted by the addition of either recombinant NGAL or FRO conditioned medium. In addition, we show that the prosurvival activity of NGAL is mediated by its ability to bind and transport iron inside the cells. Our data suggest that NF-[kappa]B contributes to thyroid tumor cell survival by controlling iron uptake via NGAL.

Details

Language :
English
ISSN :
00278424
Volume :
105
Issue :
37
Database :
Gale General OneFile
Journal :
Proceedings of the National Academy of Sciences of the United States
Publication Type :
Academic Journal
Accession number :
edsgcl.186319868