Affiliations: [a] Medical Oncology Service, Virgen de la Victoria University Hospital, E-29010 Malaga, Spain | [b] Department of Pathology, Virgen de la Victoria University Hospital, E-29010 Malaga, Spain | [c] Department of Pathology, Faculty of Medicine, University of Malaga, E-29010 Malaga, Spain | [d] Colorectal Surgery Unit, Virgen de la Victoria University Hospital, E-29010 Malaga, Spain
Correspondence:
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Corresponding author: Dr. F. Jesus Gonzalez, Medical Oncology Service, Virgen de la Victoria University Hospital, Campus de Teatinos s/n, 29010-Malaga, Spain. Tel.: +34 951 032231; Fax: +34 951 032005; E-mail: [email protected].
Abstract: Objetive:Angiogenesis is stimulated by angiogenic factors released by tumour cells, though other cells, such as tumour-associated macrophages (TAMs), also contribute towards increasing the angiogenic process in colorectal cancer (CRC). The aim of this study was to determine in CRC patients the contribution of vascular endothelial growth factor (VEGF) expression in TAMs and tumour cells towards circulating VEGF levels, their association with p53 expression and microvascular density (MVD), and their prognostic value. Methods:Immunohistochemical techniques were used to identify TAMs and p53 protein, and to evaluate the VEGF expression in TAMs, MVD and tumour cells in 110 primary CRC patients. Serum VEGF levels were determined using an enzyme immune assay. Results:There was a greater expression of VEGF in tumours with a positive p53 expression than a negative stain (p<0.01). The macrophage index was not related to tumour VEGF secretion. No significant association was observed between serum VEGF levels and VEGF tumour expression, node status, histological grade, MVD or p53 expression. However, the patients with high values of VEGF expression in TAMs showed significantly higher presurgery serum VEGF levels than those patients with low values of VEGF expression in TAMs (p=0.021). No statistical significant differences in survival were found when we compared patients with high VEGF expression in TAMs vs low or median VEGF expression in TAMs (p=0.093). Serum VEGF levels were increased 6–8 hours after tumour removal (p=0.001). Conclusions:Our data suggest that in primary CRC, presurgery circulating VEGF levels are related to VEGF produced by TAMs.
