Single nucleotide polymorphisms and mRNA expression of VEGF-A in papillary thyroid carcinoma: potential markers for aggressive phenotypes.

BACKGROUND AND OBJECTIVES Polymorphisms of the VEGF gene are known to affect the biological behaviour of cancers but have seldom been studied in thyroid cancer. The aim of the current study is to evaluate the prevalence and relevance of VEGF-A polymorphisms and mRNA expression in papillary thyroid carcinoma (PTC). MATERIALS AND METHODS Genomic DNA and total RNA were isolated from paraffin-embedded tissue from 91 PTC (51 conventional PTC and 40 follicular variant) and 78 control thyroid tissues. Three DNA polymorphisms (+936C > T, +405C > G and -141A > C) in the 3' and 5' untranslated region (3'-UTR, 5'-UTR) of VEGF-A were studied using PCR and RFLP. Also, the mRNA expression of VEGF-A in these tissues was studied by real-time PCR. RESULTS Distribution of polymorphisms in the 5'-UTR (VEGF-VEGF -141A > C and +405C > G) and 3'-UTR (VEGF +936C > T) were all significantly different in PTC and benign thyroid tissue (p = 0.0001, 0.001 and 0.028 respectively). The VEGF -141 C allele was more common in PTC with lymph node metastases (p = 0.026). VEGF + 405 Galleles andVEGF +936 CC genotype were more common in PTC of advanced pathological staging (p = 0.018 and 0.017 respectively). Also, increased expression of VEGF-A mRNA was noted in PTC compared to control (p = 0.009). Within the group of patients with conventional PTC, those with lymph nodal metastases had a higher level of VEGF-A mRNA expression than other patients (p = 0.0003). CONCLUSION These findings suggest that VEGF polymorphisms and mRNA expression may predict the aggressiveness behaviour of thyroid cancer.

[1]  Thomas D. Schmittgen,et al.  Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. , 2001, Methods.

[2]  A. Salajegheh,et al.  Follicular variant of papillary thyroid carcinoma: a diagnostic challenge for clinicians and pathologists , 2008, Postgraduate Medical Journal.

[3]  V. Mittal,et al.  Expression of Estrogen Receptor, Progesterone Receptor, and Vascular Endothelial Growth Factor-A in Thyroid Cancer , 2009, The American surgeon.

[4]  L. Bondeson Tumours of the thyroid and parathyroid , 2004 .

[5]  Q. Duh,et al.  Vascular endothelial growth factor expression is higher in differentiated thyroid cancer than in normal or benign thyroid. , 1997, The Journal of clinical endocrinology and metabolism.

[6]  W. Renner,et al.  A Common 936 C/T Mutation in the Gene for Vascular Endothelial Growth Factor Is Associated with Vascular Endothelial Growth Factor Plasma Levels , 2000, Journal of Vascular Research.

[7]  J. Folkman Tumor angiogenesis. , 1985, Advances in cancer research.

[8]  M. Bottomley,et al.  Identification of polymorphisms within the vascular endothelial growth factor (VEGF) gene: correlation with variation in VEGF protein production. , 2000, Cytokine.

[9]  J. Luk,et al.  The potential clinical relevance of serum vascular endothelial growth factor (VEGF) and VEGF-C in recurrent papillary thyroid carcinoma. , 2008, Surgery.

[10]  J. Park,et al.  Vascular Endothelial Growth Factor Gene Polymorphisms and Risk of Primary Lung Cancer , 2005, Cancer Epidemiology Biomarkers & Prevention.

[11]  P. Mathieson,et al.  Steroid-sensitive nephrotic syndrome and vascular endothelial growth factor gene polymorphisms. , 2003, European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics.

[12]  J. Luk,et al.  Serum Vascular Endothelial Growth Factor C Correlates With Lymph Node Metastases and High-Risk Tumor Profiles in Papillary Thyroid Carcinoma , 2008, Annals of surgery.

[13]  Shinichiro,et al.  Carcinoma , 1906, The Hospital.

[14]  M. Ladomery,et al.  Alternative splicing in angiogenesis: the vascular endothelial growth factor paradigm. , 2007, Cancer letters.

[15]  V. Alves,et al.  Vascular endothelial growth factor expression in invasive papillary thyroid carcinoma. , 2009, Thyroid : official journal of the American Thyroid Association.

[16]  M. Ladomery,et al.  Regulation of Vascular Endothelial Growth Factor (VEGF) Splicing from Pro-angiogenic to Anti-angiogenic Isoforms , 2009, The Journal of Biological Chemistry.

[17]  J. Luk,et al.  Increased Expression of Vascular Endothelial Growth Factor C in Papillary Thyroid Carcinoma Correlates with Cervical Lymph Node Metastases , 2005, Clinical Cancer Research.

[18]  B. Lang,et al.  Classical and Follicular Variant of Papillary Thyroid Carcinoma: A Comparative Study on Clinicopathologic Features and Long-term Outcome , 2006, World Journal of Surgery.

[19]  S. Stacker,et al.  Molecular regulation of the VEGF family – inducers of angiogenesis and lymphangiogenesis , 2004, APMIS : acta pathologica, microbiologica, et immunologica Scandinavica.

[20]  L. Mariani,et al.  Expression of angiogenesis stimulators and inhibitors in human thyroid tumors and correlation with clinical pathological features. , 1999, The American journal of pathology.

[21]  G. Heinze,et al.  Vascular endothelial growth factor gene polymorphisms in ovarian cancer. , 2007, Gynecologic oncology.

[22]  C. Lohse,et al.  Observer Variation in the Diagnosis of Follicular Variant of Papillary Thyroid Carcinoma , 2004, The American journal of surgical pathology.

[23]  Laura A. Sullivan,et al.  The VEGF family in cancer and antibody-based strategies for their inhibition , 2010, mAbs.

[24]  D. Ray,et al.  VEGF polymorphisms are associated with severity of diabetic retinopathy. , 2008, Investigative ophthalmology & visual science.

[25]  S. Juo,et al.  Vascular endothelial growth factor gene polymorphisms in thyroid cancer. , 2007, The Journal of endocrinology.

[26]  B. Paulweber,et al.  A common 936 C/T gene polymorphism of vascular endothelial growth factor is associated with decreased breast cancer risk , 2003, International journal of cancer.

[27]  K. Lam,et al.  Papillary carcinoma of thyroid: A 30-yr clinicopathological review of the histological variants , 2005, Endocrine pathology.