[BRAF initiating mutations in the papillary thyroid carcinoma].

Abstract:

:Among genetic alterations most important for the initiation of papillary thyroid carcinoma (PTC) is mutation T1799A in the BRAF gene which is the most frequent event (54.5%) in this type of thyroid cancer. It is seen in all stages, from microcarcinoma through clinically overt disease to anaplastic cancer. It has been shown that BRAF mutation is correlated with PTC histotype. It is identified most frequently in classical PTC and in tall cell variant. Moreover, BRAF mutation is described more often in older patients, whereas in young patients RET/PTC rearrangements dominate. In PTC cases with BRAF mutation V600E the prognosis is poorer, with more cancer invasiveness, metastasis and recurrence. The presence of BRAF mutation is related to the specific gene expression signature, different than in cancer cases showing RET/PTC rearrangement or no known initiating mutation.

journal_name

Endokrynol Pol

journal_title

Endokrynologia Polska

authors

Rusinek D,Gubała E

subject

Has Abstract

pub_date

2006-07-01 00:00:00

pages

438-44

issue

4

eissn

0423-104X

issn

2299-8306

journal_volume

57

pub_type

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