Thymidine phosphorylase expression in normal, hyperplastic and neoplastic prostates: correlation with tumour associated macrophages, infiltrating lymphocytes, and angiogenesis.

Thymidine phosphorylase is an angiogenic factor primarily expressed by cancer cells, stromal cells and tumour-associated macrophages in many human malignancies. These different types of thymidine phosphorylase-expressing cells, however, may have a distinct place in the angiogenic process, and this q...

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Main Authors: Sivridis, E, Giatromanolaki, A, Papadopoulos, I, Gatter, K, Harris, A, Koukourakis, M
Format: Journal article
Language:English
Published: 2002
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author Sivridis, E
Giatromanolaki, A
Papadopoulos, I
Gatter, K
Harris, A
Koukourakis, M
author_facet Sivridis, E
Giatromanolaki, A
Papadopoulos, I
Gatter, K
Harris, A
Koukourakis, M
author_sort Sivridis, E
collection OXFORD
description Thymidine phosphorylase is an angiogenic factor primarily expressed by cancer cells, stromal cells and tumour-associated macrophages in many human malignancies. These different types of thymidine phosphorylase-expressing cells, however, may have a distinct place in the angiogenic process, and this question was addressed in the present study. A series of 20 normal/hyperplastic prostate glands and 60 prostate carcinomas was investigated by immunohistochemistry, using specific antibodies for thymidine phosphorylase (P-GF.44C), tumour-associated macrophages (CD68), endothelium (CD31) and prostate specific antigen (ER-PR8). Thymidine phosphorylase expression by normal and hyperplastic epithelial or stromal cells occurred almost exclusively in the context of an intense lymphocytic infiltrate. High thymidine phosphorylase cancer cells and thymidine phosphorylase stromal cells expression was associated with high angiogenesis in prostate carcinomas, and this significant association was extended to include both tumour-associated macrophages and tumour-infiltrating lymphocytes. Thymidine phosphorylase expression and tumour-infiltrating lymphocytes were related inversely with prostate specific antigen reactivity. In conclusion, thymidine phosphorylase is a major angiogenic factor in prostate carcinomas and its up-regulation is likely to occur in the context of a host immune response.
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spelling oxford-uuid:3545e920-0c5a-4df1-a93c-f08907bae63a2022-03-26T13:31:00ZThymidine phosphorylase expression in normal, hyperplastic and neoplastic prostates: correlation with tumour associated macrophages, infiltrating lymphocytes, and angiogenesis.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:3545e920-0c5a-4df1-a93c-f08907bae63aEnglishSymplectic Elements at Oxford2002Sivridis, EGiatromanolaki, APapadopoulos, IGatter, KHarris, AKoukourakis, MThymidine phosphorylase is an angiogenic factor primarily expressed by cancer cells, stromal cells and tumour-associated macrophages in many human malignancies. These different types of thymidine phosphorylase-expressing cells, however, may have a distinct place in the angiogenic process, and this question was addressed in the present study. A series of 20 normal/hyperplastic prostate glands and 60 prostate carcinomas was investigated by immunohistochemistry, using specific antibodies for thymidine phosphorylase (P-GF.44C), tumour-associated macrophages (CD68), endothelium (CD31) and prostate specific antigen (ER-PR8). Thymidine phosphorylase expression by normal and hyperplastic epithelial or stromal cells occurred almost exclusively in the context of an intense lymphocytic infiltrate. High thymidine phosphorylase cancer cells and thymidine phosphorylase stromal cells expression was associated with high angiogenesis in prostate carcinomas, and this significant association was extended to include both tumour-associated macrophages and tumour-infiltrating lymphocytes. Thymidine phosphorylase expression and tumour-infiltrating lymphocytes were related inversely with prostate specific antigen reactivity. In conclusion, thymidine phosphorylase is a major angiogenic factor in prostate carcinomas and its up-regulation is likely to occur in the context of a host immune response.
spellingShingle Sivridis, E
Giatromanolaki, A
Papadopoulos, I
Gatter, K
Harris, A
Koukourakis, M
Thymidine phosphorylase expression in normal, hyperplastic and neoplastic prostates: correlation with tumour associated macrophages, infiltrating lymphocytes, and angiogenesis.
title Thymidine phosphorylase expression in normal, hyperplastic and neoplastic prostates: correlation with tumour associated macrophages, infiltrating lymphocytes, and angiogenesis.
title_full Thymidine phosphorylase expression in normal, hyperplastic and neoplastic prostates: correlation with tumour associated macrophages, infiltrating lymphocytes, and angiogenesis.
title_fullStr Thymidine phosphorylase expression in normal, hyperplastic and neoplastic prostates: correlation with tumour associated macrophages, infiltrating lymphocytes, and angiogenesis.
title_full_unstemmed Thymidine phosphorylase expression in normal, hyperplastic and neoplastic prostates: correlation with tumour associated macrophages, infiltrating lymphocytes, and angiogenesis.
title_short Thymidine phosphorylase expression in normal, hyperplastic and neoplastic prostates: correlation with tumour associated macrophages, infiltrating lymphocytes, and angiogenesis.
title_sort thymidine phosphorylase expression in normal hyperplastic and neoplastic prostates correlation with tumour associated macrophages infiltrating lymphocytes and angiogenesis
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AT papadopoulosi thymidinephosphorylaseexpressioninnormalhyperplasticandneoplasticprostatescorrelationwithtumourassociatedmacrophagesinfiltratinglymphocytesandangiogenesis
AT gatterk thymidinephosphorylaseexpressioninnormalhyperplasticandneoplasticprostatescorrelationwithtumourassociatedmacrophagesinfiltratinglymphocytesandangiogenesis
AT harrisa thymidinephosphorylaseexpressioninnormalhyperplasticandneoplasticprostatescorrelationwithtumourassociatedmacrophagesinfiltratinglymphocytesandangiogenesis
AT koukourakism thymidinephosphorylaseexpressioninnormalhyperplasticandneoplasticprostatescorrelationwithtumourassociatedmacrophagesinfiltratinglymphocytesandangiogenesis