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spelling paper:paper_10463976_v21_n3_p154_Cristina2023-06-08T16:01:13Z VEGF and CD31 association in pituitary adenomas Angiogenesis CD31 Pelioisis Pituitary adenoma Proliferation VEGF CD31 antigen cycline Ki 67 antigen vasculotropin adult age angiogenesis article carcinogenesis cell proliferation correlation analysis disease course epithelium cell female gender growth hormone secreting adenoma histopathology human human tissue hypophysis adenoma major clinical study male mutation priority journal prolactinoma protein expression tumor growth Western blotting Adenoma Adult Antigens, CD31 Blotting, Western Female Humans Male Pituitary Neoplasms Tumor Markers, Biological Vascular Endothelial Growth Factor A Pituitary tumors are usually less vascularized than the normal pituitary, and the role of angiogenesis in these adenomas is contentious. Appraisal of microvascular density and expression of the potent angiogenic vascular endothelial growth factor (VEGF) by immunohistochemistry has yielded controversial results, as a broad spectrum of immunostaining can be found. We determined the protein expression of VEGF and CD31, an endothelial marker, in a series of 56 surgically removed pituitary adenomas using Western blot assay. Prolactinomas had higher VEGF protein expression compared to nonfunctioning or ACTH- and GH-secreting adenomas, while CD31 was similar in the different adenoma histotypes. VEGF and CD31 were not affected by sex, age, years of adenoma evolution, or proliferation rate (Ki67 and PCNA) for all adenoma types. Only in nonfunctioning adenomas CD31 concentration increased significantly with age. There was a positive correlation between CD31 and VEGF expression when all adenoma histotypes were considered, or when prolactinomas and nonfunctioning adenomas were evaluated separately. The positive association of VEGF and CD31 expression suggests the participation of angiogenesis in adenoma development, while epithelial cell proliferation in pituitary tumors is not directly related to VEGF or CD31 expression, and other factors, such as primary genetic alterations may be involved. © 2010 Springer Science+Business Media, LLC. 2010 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_10463976_v21_n3_p154_Cristina http://hdl.handle.net/20.500.12110/paper_10463976_v21_n3_p154_Cristina
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Angiogenesis
CD31
Pelioisis
Pituitary adenoma
Proliferation
VEGF
CD31 antigen
cycline
Ki 67 antigen
vasculotropin
adult
age
angiogenesis
article
carcinogenesis
cell proliferation
correlation analysis
disease course
epithelium cell
female
gender
growth hormone secreting adenoma
histopathology
human
human tissue
hypophysis adenoma
major clinical study
male
mutation
priority journal
prolactinoma
protein expression
tumor growth
Western blotting
Adenoma
Adult
Antigens, CD31
Blotting, Western
Female
Humans
Male
Pituitary Neoplasms
Tumor Markers, Biological
Vascular Endothelial Growth Factor A
spellingShingle Angiogenesis
CD31
Pelioisis
Pituitary adenoma
Proliferation
VEGF
CD31 antigen
cycline
Ki 67 antigen
vasculotropin
adult
age
angiogenesis
article
carcinogenesis
cell proliferation
correlation analysis
disease course
epithelium cell
female
gender
growth hormone secreting adenoma
histopathology
human
human tissue
hypophysis adenoma
major clinical study
male
mutation
priority journal
prolactinoma
protein expression
tumor growth
Western blotting
Adenoma
Adult
Antigens, CD31
Blotting, Western
Female
Humans
Male
Pituitary Neoplasms
Tumor Markers, Biological
Vascular Endothelial Growth Factor A
VEGF and CD31 association in pituitary adenomas
topic_facet Angiogenesis
CD31
Pelioisis
Pituitary adenoma
Proliferation
VEGF
CD31 antigen
cycline
Ki 67 antigen
vasculotropin
adult
age
angiogenesis
article
carcinogenesis
cell proliferation
correlation analysis
disease course
epithelium cell
female
gender
growth hormone secreting adenoma
histopathology
human
human tissue
hypophysis adenoma
major clinical study
male
mutation
priority journal
prolactinoma
protein expression
tumor growth
Western blotting
Adenoma
Adult
Antigens, CD31
Blotting, Western
Female
Humans
Male
Pituitary Neoplasms
Tumor Markers, Biological
Vascular Endothelial Growth Factor A
description Pituitary tumors are usually less vascularized than the normal pituitary, and the role of angiogenesis in these adenomas is contentious. Appraisal of microvascular density and expression of the potent angiogenic vascular endothelial growth factor (VEGF) by immunohistochemistry has yielded controversial results, as a broad spectrum of immunostaining can be found. We determined the protein expression of VEGF and CD31, an endothelial marker, in a series of 56 surgically removed pituitary adenomas using Western blot assay. Prolactinomas had higher VEGF protein expression compared to nonfunctioning or ACTH- and GH-secreting adenomas, while CD31 was similar in the different adenoma histotypes. VEGF and CD31 were not affected by sex, age, years of adenoma evolution, or proliferation rate (Ki67 and PCNA) for all adenoma types. Only in nonfunctioning adenomas CD31 concentration increased significantly with age. There was a positive correlation between CD31 and VEGF expression when all adenoma histotypes were considered, or when prolactinomas and nonfunctioning adenomas were evaluated separately. The positive association of VEGF and CD31 expression suggests the participation of angiogenesis in adenoma development, while epithelial cell proliferation in pituitary tumors is not directly related to VEGF or CD31 expression, and other factors, such as primary genetic alterations may be involved. © 2010 Springer Science+Business Media, LLC.
title VEGF and CD31 association in pituitary adenomas
title_short VEGF and CD31 association in pituitary adenomas
title_full VEGF and CD31 association in pituitary adenomas
title_fullStr VEGF and CD31 association in pituitary adenomas
title_full_unstemmed VEGF and CD31 association in pituitary adenomas
title_sort vegf and cd31 association in pituitary adenomas
publishDate 2010
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_10463976_v21_n3_p154_Cristina
http://hdl.handle.net/20.500.12110/paper_10463976_v21_n3_p154_Cristina
_version_ 1768541715111608320