Angiogenesis and lymphangiogenesis in parathyroid proliferative lesions.
Angiogenesis and lymphangiogenesis are involved in tumoral growth and metastatic spread. There is little information on angiogenesis and no available data on lymphangiogenesis in parathyroid glands (PTG). Using immunohistochemistry for CD34, LYVE-1 (specific markers for vascular and lymphatic endoth...
Main Authors: | , , , , |
---|---|
Formato: | Journal article |
Idioma: | English |
Publicado em: |
2004
|
_version_ | 1826304759768809472 |
---|---|
author | Garcia de la Torre, N Buley, I Wass, J Jackson, D Turner, H |
author_facet | Garcia de la Torre, N Buley, I Wass, J Jackson, D Turner, H |
author_sort | Garcia de la Torre, N |
collection | OXFORD |
description | Angiogenesis and lymphangiogenesis are involved in tumoral growth and metastatic spread. There is little information on angiogenesis and no available data on lymphangiogenesis in parathyroid glands (PTG). Using immunohistochemistry for CD34, LYVE-1 (specific markers for vascular and lymphatic endothelium, respectively), vascular endothelial growth factor (VEGF)-A, VEGF-C, and fibroblast growth factor (FGF)-2, this study analyzes microvascular density (MVD), lymphatic vascular density (LVD), and expression of angiogenic and lymphangiogenic growth factors in 13 normal PTG, 77 parathyroid adenomas (PTA), and 17 primary parathyroid hyperplasia (PPH). MVD was higher in PPH and PTA, compared with PTG (P < 0.001). There was no difference in VEGF-A expression among groups. In contrast, FGF-2 expression was higher in PPH, compared with PTA and PTG (P < 0.0001). FGF-2 scores and MVD were significantly correlated (r = 0.43). LVD did not differ among groups, and VEGF-C expression was unrelated to LVD. There was no relationship between MVD and tumor behavior (adenoma size, PTH, or calcium). In conclusion, this study shows increased angiogenesis in parathyroid proliferative lesions compared with normal glands and suggests that FGF-2 is proangiogenic in parathyroid tissue. In PTA, tumor behavior is not related to angiogenic phenotype. This is the first demonstration of lymphatic vessels in PTG, but the lack of correlation with VEGF-C expression suggests that VEGF-C is not the primary lymphangiogenic factor. |
first_indexed | 2024-03-07T06:22:39Z |
format | Journal article |
id | oxford-uuid:f333b021-e5df-4f6f-99c7-c79537f43f0e |
institution | University of Oxford |
language | English |
last_indexed | 2024-03-07T06:22:39Z |
publishDate | 2004 |
record_format | dspace |
spelling | oxford-uuid:f333b021-e5df-4f6f-99c7-c79537f43f0e2022-03-27T12:10:20ZAngiogenesis and lymphangiogenesis in parathyroid proliferative lesions.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:f333b021-e5df-4f6f-99c7-c79537f43f0eEnglishSymplectic Elements at Oxford2004Garcia de la Torre, NBuley, IWass, JJackson, DTurner, HAngiogenesis and lymphangiogenesis are involved in tumoral growth and metastatic spread. There is little information on angiogenesis and no available data on lymphangiogenesis in parathyroid glands (PTG). Using immunohistochemistry for CD34, LYVE-1 (specific markers for vascular and lymphatic endothelium, respectively), vascular endothelial growth factor (VEGF)-A, VEGF-C, and fibroblast growth factor (FGF)-2, this study analyzes microvascular density (MVD), lymphatic vascular density (LVD), and expression of angiogenic and lymphangiogenic growth factors in 13 normal PTG, 77 parathyroid adenomas (PTA), and 17 primary parathyroid hyperplasia (PPH). MVD was higher in PPH and PTA, compared with PTG (P < 0.001). There was no difference in VEGF-A expression among groups. In contrast, FGF-2 expression was higher in PPH, compared with PTA and PTG (P < 0.0001). FGF-2 scores and MVD were significantly correlated (r = 0.43). LVD did not differ among groups, and VEGF-C expression was unrelated to LVD. There was no relationship between MVD and tumor behavior (adenoma size, PTH, or calcium). In conclusion, this study shows increased angiogenesis in parathyroid proliferative lesions compared with normal glands and suggests that FGF-2 is proangiogenic in parathyroid tissue. In PTA, tumor behavior is not related to angiogenic phenotype. This is the first demonstration of lymphatic vessels in PTG, but the lack of correlation with VEGF-C expression suggests that VEGF-C is not the primary lymphangiogenic factor. |
spellingShingle | Garcia de la Torre, N Buley, I Wass, J Jackson, D Turner, H Angiogenesis and lymphangiogenesis in parathyroid proliferative lesions. |
title | Angiogenesis and lymphangiogenesis in parathyroid proliferative lesions. |
title_full | Angiogenesis and lymphangiogenesis in parathyroid proliferative lesions. |
title_fullStr | Angiogenesis and lymphangiogenesis in parathyroid proliferative lesions. |
title_full_unstemmed | Angiogenesis and lymphangiogenesis in parathyroid proliferative lesions. |
title_short | Angiogenesis and lymphangiogenesis in parathyroid proliferative lesions. |
title_sort | angiogenesis and lymphangiogenesis in parathyroid proliferative lesions |
work_keys_str_mv | AT garciadelatorren angiogenesisandlymphangiogenesisinparathyroidproliferativelesions AT buleyi angiogenesisandlymphangiogenesisinparathyroidproliferativelesions AT wassj angiogenesisandlymphangiogenesisinparathyroidproliferativelesions AT jacksond angiogenesisandlymphangiogenesisinparathyroidproliferativelesions AT turnerh angiogenesisandlymphangiogenesisinparathyroidproliferativelesions |