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PMID: 16772349 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Influence of the BRAF V600E mutation on expression of vascular endothelial growth factor in papillary thyroid cancer.

The Journal of clinical endocrinology and metabolism ·Vol. 91 ·No. 9 ·2006-09-00 ·Pages 3667-70

Jo YS, Li S, Song JH, Kwon KH, Lee JC, Rha SY, Lee HJ, Sul JY, Kweon GR, Ro HK, Kim JM, Shong M

Abstract

The BRAF mutation may influence the expression patterns of molecular markers that are related to the development and progression of thyroid cancer. The objective of the study was to investigate the effects of the BRAF V600E mutation on expression of galectin-3, cyclooxygenase-2, cyclin D1, p53, and vascular endothelial growth factor (VEGF) in papillary thyroid cancer (PTC). One hundred sixty-three PTC and 28 nodular hyperplasia patients were selected retrospectively. The presence of the BRAF V600E mutation and the level of expression of the molecular markers were determined. Of 161 PTC patients, 102 patients (63.4%) were BRAF V600E(+), and these cases had significantly larger tumor sizes (P = 0.01), compared with V600E(-) cases (n = 59, 36.6%). Although PTC tissues had higher expression levels of the selected molecular markers than nodular hyperplasia tissues, expression levels of several molecular markers in BRAF V600E(+) PTC were not significantly different from those of BRAF V600E(-) PTC. But VEGF was significantly up-regulated in BRAF V600E(+) PTC, compared with BRAF V600E(-) PTC. VEGF expression levels were strongly positively correlated to tumor size (P < 0.001), extrathyroidal invasion (P = 0.02), and tumor stage (P = 0.04). Multivariate analysis clearly showed that VEGF expression was up-regulated in BRAF V600E(+) PTC (odds ratio 2.5, confidence interval 1.1-5.6; P = 0.03). BRAF V600E(+) PTC tended to have larger tumor volumes and higher expression of VEGF. The level of VEGF expression was closely correlated with tumor size, extrathyroidal invasion, and stage. The relatively high levels of VEGF expression may be related to poorer clinical outcomes and recurrences in BRAF V600E(+) PTC.

MeSH Terms
Adult Carcinoma, Papillary/genetics,metabolism,pathology Cyclin D1/metabolism Cyclooxygenase 2/metabolism DNA, Neoplasm/chemistry,genetics Female Galectin 3/metabolism Humans Immunohistochemistry Male Middle Aged Point Mutation Polymerase Chain Reaction Proto-Oncogene Proteins B-raf/genetics Retrospective Studies Thyroid Neoplasms/genetics,metabolism,pathology Tumor Suppressor Protein p53/metabolism Vascular Endothelial Growth Factor A/biosynthesis,genetics
Chemicals
DNA, Neoplasm Galectin 3 Tumor Suppressor Protein p53 VEGFA protein, human Vascular Endothelial Growth Factor A Cyclin D1 Cyclooxygenase 2 BRAF protein, human Proto-Oncogene Proteins B-raf
Authors & Affiliations
12 authors, click to expand affiliations / ORCID
Jo Young Suk
Division of Endocrinology, Department of Internal Medicine, Chungnam National University School of Medicine, Daejeon 301-721, Korea.
Li Shengjin
Song Jung Hun
Kwon Ki Hyun
Lee Jun Chul
Rha So Young
Lee Hyo Jin
Sul Ji Young
Kweon Gi Ryang
Ro Heung-Kyu
Kim Jin-Man
Shong Minho
Article Info
Journal
The Journal of clinical endocrinology and metabolism
Abbr.
J Clin Endocrinol Metab
ISSN
0021-972X
Published
2006-09-00
Epub
2006-00-13
Pages
3667-70
Language
English
Region
United States
NLM ID
0375362
Subset
IM
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