کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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3943490 | 1254118 | 2007 | 7 صفحه PDF | دانلود رایگان |

Objectives.Vascular endothelial growth factors A and B (VEGF-A and VEGF-B) play a major role in angiogenesis and activate VEGF receptor 1 (VEGFR-1). However, the clinicopathologic and clinical value of VEGF-B and VEGFR-1 in invasive breast carcinoma remains unclear.Methods.We immunohistochemically examined the expression pattern of VEGF-A, VEGF-B and VEGFR-1 in 177 invasive breast carcinomas in relation to clinicopathological parameters, p53, c-erbB2 proteins expression and patients' survival.Results.VEGF-A, VEGF-B and VEGFR-1 were immunodetected predominantly in the cytoplasm of the malignant cells. None of the studied markers correlated with any of the clinicopathological parameters, other than stromal VEGFR-1 which inversely correlated with PR (p = 0.021). Cancerous VEGF-A and stromal VEGFR-1 were positively related to p53 (p = 0.016 and p = 0.033, respectively). Cancerous VEGF-B was positively associated with c-erbB-2 (p = 0.045) and was found to exert an unfavorable impact on both disease-free and the overall survival of the node-positive patients (p = 0.05 and p = 0.029, respectively). Cancerous VEGFR-1 was recognized as being an independent poor prognostic indicator (p = 0.037).Conclusion.These findings suggest that, while VEGF-B seems to be useful as a prognostic indicator only in node-positive patients, VEGFR-1 may be an independent poor prognosticator in patients with invasive breast carcinoma.
Journal: Gynecologic Oncology - Volume 104, Issue 3, March 2007, Pages 557–563