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Volume 41, Issue 18, Pages 2819-2827 (December 2005)


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Placenta growth factor is over-expressed and has prognostic value in human breast cancer

Christian ParraCorresponding Author Informationemail address, Gareth Watkinsa, Mike Boultonb, Jun Caib, Wen G. Jianga

Received 11 March 2005; received in revised form 19 July 2005; accepted 28 July 2005.

Abstract 

Placenta growth factor (PlGF) belongs to the vascular endothelial growth factor (VEGF) family, a group of angiogenic factors that are crucial for tumour angiogenesis. Very little is known about the significance of PlGF in human cancer. We hypothesise that PlGF may have a potent influence in breast cancer. This study examined PlGF levels in human breast cancer in relation to patient’s clinical parameters. PlGF expression and distribution was examined quantitatively using real-time quantitative polymerase chain reaction (Q-PCR) on a cohort of human breast cancer tissue (n=119) and background breast tissue (n=33), qualitatively using reverse transcriptase polymerase chain reaction (RT-PCR) on a range of cell lines, and immunohistochemically on patient samples. All these techniques revealed that PlGF expression was dramatically increased (P=0.028) in breast cancer tissues compared with normal breast tissue. We demonstrate that PlGF displays prognostic value through analysis of patient survival status (6-year follow-up), as elevated levels of PlGF were significantly associated (P=0.017) with recurrence, metastasis and patient mortality. Our study has shown that PlGF is over-expressed in breast cancer tissues and correlates with patient prognosis, and is likely to play a major role in the pathogenesis of tumours.

a Metastasis and Angiogenesis Research Group, Department of Surgery, Wales College of Medicine, Cardiff University, Heath Park, Cardiff CF14 4XN, UK

b Cell and Molecular Biology Unit, School of Optometry and Vision Sciences, Redwood Building, King Edward VII Ave., Cardiff University, Cardiff, CF10 3NB, UK

Corresponding Author InformationCorresponding author. Tel.: +44 29 2074 8394; fax: +44 29 2076 1623.

PII: S0959-8049(05)00793-8

doi:10.1016/j.ejca.2005.07.022


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