Rearrangements of NTRK1 gene in papillary thyroid carcinoma.

Abstract:

:TRK oncogenes are observed in a consistent fraction of papillary thyroid carcinoma (PTC); they arise from the fusion of the 3' terminal sequences of the NTRK1/NGF receptor gene with 5' terminal sequences of various activating genes, such as TPM3, TPR and TFG. TRK oncoproteins display constitutive tyrosine-kinase activity, leading to in vitro and in vivo transformation. In this review studies performed during the last 20 years will be summarized. The following topics will be illustrated: (a) frequency of TRK oncogenes and correlation with radiation and tumor histopathological features; (b) molecular mechanisms underlying NTRK1 oncogenic rearrangements; (c) molecular and biochemical characterization of TRK oncoproteins, and their mechanism of action; (d) role of activating sequences in the activation of TRK oncoproteins.

journal_name

Mol Cell Endocrinol

authors

Greco A,Miranda C,Pierotti MA

doi

10.1016/j.mce.2009.10.009

subject

Has Abstract

pub_date

2010-05-28 00:00:00

pages

44-9

issue

1

eissn

0303-7207

issn

1872-8057

pii

S0303-7207(09)00556-5

journal_volume

321

pub_type

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