Induction of a proinflammatory program in normal human thyrocytes by the RET/PTC1 oncogene.

Abstract:

:Rearrangements of the RET receptor tyrosine kinase gene generating RET/PTC oncogenes are specific to papillary thyroid carcinoma (PTC), the most frequent thyroid tumor. Here, we show that the RET/PTC1 oncogene, when exogenously expressed in primary normal human thyrocytes, induces the expression of a large set of genes involved in inflammation and tumor invasion, including those encoding chemokines (CCL2, CCL20, CXCL8, and CXCL12), chemokine receptors (CXCR4), cytokines (IL1B, CSF-1, GM-CSF, and G-CSF), matrix-degrading enzymes (metalloproteases and urokinase-type plasminogen activator and its receptor), and adhesion molecules (L-selectin). This effect is strictly dependent on the presence of the RET/PTC1 Tyr-451 (corresponding to RET Tyr-1062 multidocking site). Selected relevant genes (CCL20, CCL2, CXCL8, CXCR4, L-selectin, GM-CSF, IL1B, MMP9, UPA, and SPP1/OPN) were found up-regulated also in clinical samples of PTC, particularly those characterized by RET/PTC activation, local extrathyroid spread, and lymph node metastases, when compared with normal thyroid tissue or follicular thyroid carcinoma. These results, demonstrating that the RET/PTC1 oncogene activates a proinflammatory program, provide a direct link between a transforming human oncogene, inflammation, and malignant behavior.

authors

Borrello MG,Alberti L,Fischer A,Degl'innocenti D,Ferrario C,Gariboldi M,Marchesi F,Allavena P,Greco A,Collini P,Pilotti S,Cassinelli G,Bressan P,Fugazzola L,Mantovani A,Pierotti MA

doi

10.1073/pnas.0503039102

keywords:

subject

Has Abstract

pub_date

2005-10-11 00:00:00

pages

14825-30

issue

41

eissn

0027-8424

issn

1091-6490

pii

0503039102

journal_volume

102

pub_type

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