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Angiogenesis in cancer of unknown primary: clinicopathological study of CD34, VEGF and TSP-1

BACKGROUND: Cancer of unknown primary remains a mallignancy of elusive biology and grim prognosis that lacks effective therapeutic options. We investigated angiogenesis in cancer of unknown primary to expand our knowledge on the biology of these tumors and identify potential therapeutic targets. MET...

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Autores principales: Karavasilis, Vasilis, Malamou-Mitsi, Vasiliki, Briasoulis, Evangelos, Tsanou, Elena, Kitsou, Evangelia, Kalofonos, Haralambos, Fountzilas, George, Fotsis, Theodore, Pavlidis, Nicholas
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC555600/
https://www.ncbi.nlm.nih.gov/pubmed/15743540
http://dx.doi.org/10.1186/1471-2407-5-25
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author Karavasilis, Vasilis
Malamou-Mitsi, Vasiliki
Briasoulis, Evangelos
Tsanou, Elena
Kitsou, Evangelia
Kalofonos, Haralambos
Fountzilas, George
Fotsis, Theodore
Pavlidis, Nicholas
author_facet Karavasilis, Vasilis
Malamou-Mitsi, Vasiliki
Briasoulis, Evangelos
Tsanou, Elena
Kitsou, Evangelia
Kalofonos, Haralambos
Fountzilas, George
Fotsis, Theodore
Pavlidis, Nicholas
author_sort Karavasilis, Vasilis
collection PubMed
description BACKGROUND: Cancer of unknown primary remains a mallignancy of elusive biology and grim prognosis that lacks effective therapeutic options. We investigated angiogenesis in cancer of unknown primary to expand our knowledge on the biology of these tumors and identify potential therapeutic targets. METHODS: Paraffin embedded archival material from 81 patients diagnosed with CUP was used. Tumor histology was adenocarcinoma (77%), undifferentiated carcinoma (18%) and squamous cell carcinoma (5%). The tissue expression of CD34, VEGF and TSP-1 was assessed immunohistochemically by use of specific monoclonal antibodies and was analyzed against clinicopathological data. RESULTS: VEGF expression was detected in all cases and was strong in 83%. Stromal expression of TSP-1 was seen in 80% of cases and was strong in 20%. The expression of both proteins was not associated with any clinical or pathological parameters. Tumor MVD was higher in tumors classified as unfavorable compared to more favorable and was positively associated with VEGF and negatively with TSP-1. CONCLUSION: Angiogenesis is very active and expression of VEGF is almost universal in cancers of unknown primary. These findings support the clinical investigation of VEGF targeted therapy in this clinical setting.
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spelling pubmed-5556002005-03-28 Angiogenesis in cancer of unknown primary: clinicopathological study of CD34, VEGF and TSP-1 Karavasilis, Vasilis Malamou-Mitsi, Vasiliki Briasoulis, Evangelos Tsanou, Elena Kitsou, Evangelia Kalofonos, Haralambos Fountzilas, George Fotsis, Theodore Pavlidis, Nicholas BMC Cancer Research Article BACKGROUND: Cancer of unknown primary remains a mallignancy of elusive biology and grim prognosis that lacks effective therapeutic options. We investigated angiogenesis in cancer of unknown primary to expand our knowledge on the biology of these tumors and identify potential therapeutic targets. METHODS: Paraffin embedded archival material from 81 patients diagnosed with CUP was used. Tumor histology was adenocarcinoma (77%), undifferentiated carcinoma (18%) and squamous cell carcinoma (5%). The tissue expression of CD34, VEGF and TSP-1 was assessed immunohistochemically by use of specific monoclonal antibodies and was analyzed against clinicopathological data. RESULTS: VEGF expression was detected in all cases and was strong in 83%. Stromal expression of TSP-1 was seen in 80% of cases and was strong in 20%. The expression of both proteins was not associated with any clinical or pathological parameters. Tumor MVD was higher in tumors classified as unfavorable compared to more favorable and was positively associated with VEGF and negatively with TSP-1. CONCLUSION: Angiogenesis is very active and expression of VEGF is almost universal in cancers of unknown primary. These findings support the clinical investigation of VEGF targeted therapy in this clinical setting. BioMed Central 2005-03-03 /pmc/articles/PMC555600/ /pubmed/15743540 http://dx.doi.org/10.1186/1471-2407-5-25 Text en Copyright © 2005 Karavasilis et al; licensee BioMed Central Ltd.
spellingShingle Research Article
Karavasilis, Vasilis
Malamou-Mitsi, Vasiliki
Briasoulis, Evangelos
Tsanou, Elena
Kitsou, Evangelia
Kalofonos, Haralambos
Fountzilas, George
Fotsis, Theodore
Pavlidis, Nicholas
Angiogenesis in cancer of unknown primary: clinicopathological study of CD34, VEGF and TSP-1
title Angiogenesis in cancer of unknown primary: clinicopathological study of CD34, VEGF and TSP-1
title_full Angiogenesis in cancer of unknown primary: clinicopathological study of CD34, VEGF and TSP-1
title_fullStr Angiogenesis in cancer of unknown primary: clinicopathological study of CD34, VEGF and TSP-1
title_full_unstemmed Angiogenesis in cancer of unknown primary: clinicopathological study of CD34, VEGF and TSP-1
title_short Angiogenesis in cancer of unknown primary: clinicopathological study of CD34, VEGF and TSP-1
title_sort angiogenesis in cancer of unknown primary: clinicopathological study of cd34, vegf and tsp-1
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC555600/
https://www.ncbi.nlm.nih.gov/pubmed/15743540
http://dx.doi.org/10.1186/1471-2407-5-25
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