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Expression of the vascular endothelial growth factor receptor-2/Fik-1 in breast carcinomas: Correlation with proliferation

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dc.contributor.author Nakopoulou, L en
dc.contributor.author Stefanaki, K en
dc.contributor.author Panayotopoulou, E en
dc.contributor.author Giannopoulou, I en
dc.contributor.author Athanassiadou, P en
dc.contributor.author Gakiopoulou-Givalou, H en
dc.contributor.author Louvrou, A en
dc.date.accessioned 2014-03-01T01:52:05Z
dc.date.available 2014-03-01T01:52:05Z
dc.date.issued 2002 en
dc.identifier.issn 0046-8177 en
dc.identifier.uri https://dspace.lib.ntua.gr/xmlui/handle/123456789/26553
dc.subject fetal liver kinase (Flk-1)/KDR en
dc.subject breast cancer en
dc.subject proliferation en
dc.subject.classification Pathology en
dc.subject.other TUMOR ANGIOGENESIS en
dc.subject.other TISSUE INHIBITOR en
dc.subject.other FACTOR VEGF en
dc.subject.other IN-VIVO en
dc.subject.other MELANOMA-CELLS en
dc.subject.other CANCER en
dc.subject.other RECEPTORS en
dc.subject.other FLK-1 en
dc.subject.other VASCULOGENESIS en
dc.subject.other ANTIBODY en
dc.title Expression of the vascular endothelial growth factor receptor-2/Fik-1 in breast carcinomas: Correlation with proliferation en
heal.type journalArticle en
heal.language English en
heal.publicationDate 2002 en
heal.abstract Vascular endothelial growth factor (VEGF) and its receptor Flk-1/KDR play an important role in vascular permeability and tumor angiogenesis. Prompted by the hypothesis that VEGF/Flk-1 system may have regulatory roles in breast carcinogenesis, we investigated the expression of Flk-1 in 141 invasive breast carcinomas in correlation with clinical and immunohistochemical prognostic parameters, including proliferation indices like Ki-67 and Topoisomerase Ha (Topo-Ha). The immunohistochemical avidin-biotin-peroxidase method was performed on paraffin sections for the detection of Flk-1, p53, Bcl-2, c-erbB-2, M-67, Topo-Ha, ER, and PR. Flk-1 was detected in 91 of 141 (64.5%) of invasive breast carcinomas showing a widespread cytoplasmic expression in most of the neoplastic cells. Flk-1 expression was correlated with the menopausal status (P = 0.051) of the patient and the nuclear grade of the invasive breast carcinoma (P = 0.003), but demonstrated no correlation with histologic grade, stage, and patient survival. It is interesting that Flk-1 expression demonstrated a significant correlation with 2 well-established proliferation indices, Ki-67 (P = 0.037) and topo-IIalpha (P = 0.009), whereas there was no correlation with the expression of ER, PR, p53, Bcl-2, and c-erbB-2. Moreover, Flk-1 expression showed an inverse correlation with TIMP-I mRNA localization in intratumoral stromal cells (P = 0.013). In conclusion, the significant correlation of Flk-1 expression in invasive breast carcinomas with proliferation indices like Ki-67 and topo-IIa suggests that VEGF may exert a growth factor activity on mammary cancer cells through its receptor Flk-1. On the other hand, the inverse correlation of Flk-1 with TIMP-1 mRNA in intratumoral stromal cells supports the notion that TIMP-1 may have an inhibitory role on angiogenesis. Copyright 2002, Elsevier Science (USA). All rights reserved. en
heal.publisher W B SAUNDERS CO en
heal.journalName HUMAN PATHOLOGY en
dc.identifier.isi ISI:000178282800002 en
dc.identifier.volume 33 en
dc.identifier.issue 9 en
dc.identifier.spage 863 en
dc.identifier.epage 870 en


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