BRAF(V600E) mutation and the biology of papillary thyroid cancer.

TitleBRAF(V600E) mutation and the biology of papillary thyroid cancer.
Publication TypeJournal Article
Year of Publication2008
AuthorsFrasca F, Nucera C, Pellegriti G, Gangemi P, Attard M, Stella M, Loda M, Vella V, Giordano C, Trimarchi F, Mazzon E, Belfiore A, Vigneri R
JournalEndocr Relat Cancer
Volume15
Issue1
Pagination191-205
Date Published2008 Mar
ISSN1351-0088
KeywordsCarcinoma, Papillary, Disease Progression, DNA Primers, Female, Follow-Up Studies, Geography, Humans, Immunoenzyme Techniques, Lasers, Lymphatic Metastasis, Male, Matrix Metalloproteinase 9, Microdissection, Middle Aged, Mutation, Neoplasm Invasiveness, Proto-Oncogene Proteins B-raf, Reverse Transcriptase Polymerase Chain Reaction, RNA, Messenger, Sicily, Thyroid Neoplasms
Abstract

BRAF((V600E)) mutation is the most frequent genetic alteration in papillary thyroid carcinomas (PTCs) that are 80-90% of all thyroid cancers. We evaluated the relationship between BRAF((V600E)) and tumor, host, and environmental factors in PTCs from all geographical areas of Sicily. By PCR, BRAF((V600E)) was investigated in a series of 323 PTCs diagnosed in 2002-2005. The correlation between clinicopathological tumor, host, and environmental characteristics and the presence of BRAF((V600E)) were evaluated by both univariate and multivariate analyses. BRAF((V600E)) was found in 38.6% PTCs, with a 52% frequency in the classical PTCs and 26.4% in the tall cell variant. Univariate analysis indicated that BRAF((V600E)) was associated with greater tumor size (P=0.0048), extra-thyroid invasion (P<0.0001), and cervical lymph nodal metastases (P=0.0001). Multivariate logistic regression analysis confirmed that BRAF((V600E)) was an independent predictor of extra-thyroid invasion (P=0.0001) and cervical lymph nodal metastasis (P=0.0005). The association between BRAF((V600E)) and extra-thyroid invasion was also found in micro-PTCs (P=0.006). In 60 classical PTCs, BRAF((V600E)) was positively correlated with matrix metalloproteinase-9 expression (P=0.0047), suggesting a possible mechanism for BRAF((V600E)) effect on PTC invasiveness. No association was found between BRAF((V600E)) and patient age, gender, or iodine intake. In contrast, a strong association was found with residency in Eastern Sicily (P<0.0001 compared with Western Sicily). These results indicate that BRAF((V600E)) mutation is a marker of aggressive disease in both micro- and macro-PTCs. Moreover, for the first time, a possible link between BRAF((V600E)) mutation and environmental carcinogens is suggested.

DOI10.1677/ERC-07-0212
Alternate JournalEndocr Relat Cancer
PubMed ID18310287
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