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Title: Angiogenic and lymphangiogenic profiles in histological variants of papillary thyroid carcinoma
Authors: Skuletić V.
Radosavljevic, Gordana
Pantic, Jelena
Markovic B.
Jovanovic I.
Janković, Nenad
Petrovic, Dejan
Jevtovic A.
Dzodic, Radan
Arsenijevic, Nebojsa
Issue Date: 2017
Abstract: © Medycyna Praktyczna, Kraków 2017. Introduction Papillary thyroid carcinoma (PTC) is a well-differentiated tumor that occurs in several histological variants whose biological behaviors remain unclear. Angiogenesis and lymphangiogenesis are critical processes that enable tumor progression. Objectives The aim of this study was to evaluate the angiogenic and lymphangiogenic phenotypes of PTC, considering the differences between histological variants. Patient s an d met hods Angiogenic and lymphangiogenic profiles were analyzed by determining microvascular density (MVD) and lymphatic vessel density (LVD) in 73 cases of PTC, using immunohistochemistry. To assess the biological markers involved in blood and lymph vessel formation, the expression of vascular endothelial growth factor (VEGF), cyclooxygenase 2 (COX-2), and p27kip1 (p27) was determined. Result s MVD was significantly higher in patients with high-risk PTC and in those with local extrathyroidal and vascular invasion. Positive VEGF expression was strongly associated with high MVD and age-related tumor enlargement. The presence of lymph vessel invasion was associated with the expression of either VEGF or COX-2. The analysis of angiogenesis and lymphangiogenesis in different histological variants of PTC revealed elevated LVD rather than MVD in the follicular variant of PTC (FV-PTC). Lower MVD was observed in FV-PTC relative to the classic variant of PTC (CV-PTC). The frequency of VEGF-positive tumors was higher in CV-PTC than in FV-PTC. A significant association between COX-2 and p27 expression was observed in FV-PTC but not in CV-PTC. Conclusions These results suggest that VEGF, COX-2, and p27 may be important biological markers that determine the angiogenic and lymphangiogenic potentials of PTC, particularly between the follicular and classic variants.
Type: article
DOI: 10.20452/pamw.3999
ISSN: 0032-3772
SCOPUS: 2-s2.0-85021785925
Appears in Collections:Faculty of Medical Sciences, Kragujevac
Institute for Information Technologies, Kragujevac

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