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dc.contributor.authorKaravasilis, V.en
dc.contributor.authorMalamou-Mitsi, Vassiliki D.en
dc.contributor.authorBriassoulis, E. Chen
dc.contributor.authorTsanou, E.en
dc.contributor.authorKitsou, E.en
dc.contributor.authorKalofonos, H. P.en
dc.contributor.authorFountzilas, Georgeen
dc.contributor.authorFotsis, T.en
dc.contributor.authorPavlidis, Nicholasen
dc.creatorKaravasilis, V.en
dc.creatorMalamou-Mitsi, Vassiliki D.en
dc.creatorBriassoulis, E. Chen
dc.creatorTsanou, E.en
dc.creatorKitsou, E.en
dc.creatorKalofonos, H. P.en
dc.creatorFountzilas, Georgeen
dc.creatorFotsis, T.en
dc.creatorPavlidis, Nicholasen
dc.date.accessioned2018-06-22T09:53:44Z
dc.date.available2018-06-22T09:53:44Z
dc.date.issued2005
dc.identifier.urihttps://gnosis.library.ucy.ac.cy/handle/7/41999
dc.description.abstractBackground: 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. © 2005 Karavasilis et al; licensee BiioMed Central Ltd.en
dc.language.isoengen
dc.sourceBMC Canceren
dc.subjectArticleen
dc.subjectAntineoplastic agenten
dc.subjectHumanen
dc.subjectNeoplasmsen
dc.subject80 and overen
dc.subjectAgeden
dc.subjectBrain neoplasmsen
dc.subjectHumansen
dc.subjectAdulten
dc.subjectAgeden
dc.subjectControlled studyen
dc.subjectFemaleen
dc.subjectMajor clinical studyen
dc.subjectPlatinum derivativeen
dc.subjectHuman tissueen
dc.subjectMetastasisen
dc.subjectBrain tumoren
dc.subjectMaleen
dc.subjectAntigensen
dc.subjectImmunohistochemistryen
dc.subjectProtein expressionen
dc.subjectMonoclonal antibodyen
dc.subjectHistopathologyen
dc.subjectCancer adjuvant therapyen
dc.subjectPathologyen
dc.subjectTumor vascularizationen
dc.subjectVasculotropinen
dc.subjectBrain metastasisen
dc.subjectMiddle ageden
dc.subjectAdenocarcinomaen
dc.subjectSquamous cell carcinomaen
dc.subjectBiologicalen
dc.subjectTumor markersen
dc.subjectCancer of unknown primary siteen
dc.subjectUnknown primaryen
dc.subjectCarcinomaen
dc.subjectUndifferentiated carcinomaen
dc.subjectTumor markeren
dc.subjectCancer classificationen
dc.subjectParaffinen
dc.subjectBrain radiationen
dc.subjectCd34en
dc.subjectCd34 antigenen
dc.subjectChemistryen
dc.subjectNeovascularizationen
dc.subjectNeovascularization (pathology)en
dc.subjectPathologicen
dc.subjectThrombospondin 1en
dc.subjectVascular endothelial growth factor aen
dc.subjectVascularizationen
dc.subjectVasculotropin aen
dc.subjectVegfa proteinen
dc.titleAngiogenesis in cancer of unknown primary: Clinicopathological study of CD34, VEGF and TSP-1en
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1186/1471-2407-5-25
dc.description.volume5
dc.author.facultyΙατρική Σχολή / Medical School
dc.author.departmentΙατρική Σχολή / Medical School
dc.type.uhtypeArticleen
dc.contributor.orcidPavlidis, Nicholas [0000-0002-2195-9961]
dc.contributor.orcidKaravasilis, V. [0000-0002-5806-9399]
dc.contributor.orcidKalofonos, H. P. [0000-0002-3286-778X]
dc.gnosis.orcid0000-0002-2195-9961
dc.gnosis.orcid0000-0002-5806-9399
dc.gnosis.orcid0000-0002-3286-778X


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