Loss of CD59 expression in breast tumours correlates with poor survival
- 18 March 2003
- journal article
- research article
- Published by Wiley in The Journal of Pathology
- Vol. 200 (5) , 633-639
- https://doi.org/10.1002/path.1357
Abstract
CD59 (protectin), a phosphatidylinositol‐anchored glycoprotein, is a member of the cell membrane‐bound complement regulatory proteins that inhibits the formation of the terminal membrane attack complex (MAC) of complement. In this study, the expression of CD59 was evaluated in 520 breast carcinomas from patients with a mean follow‐up of 87 months. This expression was correlated with clinicopathological features and patient survival. Marked variation in the intensity of CD59 expression, which correlated with histological grade and Nottingham prognostic index (NPI), was found, with higher expression of CD59 found more often in well and moderately differentiated tumours and those of good prognosis (NPI ≤ 3.4). In contrast, high grade and poor prognosis (NPI > 5.4) carcinomas significantly demonstrated lack of CD59 expression (p < 0.001). Moreover, it was found that the percentage of CD59‐positive cells correlated significantly with patient survival, ie patients with a high percentage of positive cells (>50%) had a better overall survival (p = 0.006). A correlation was also found between the percentage of CD59‐positive cells and tumour type and also the development of distant metastases. No association was found between either the intensity or the percentage of cells expressing CD59 and vascular invasion, lymph node stage, tumour size, patient age or menopausal status. In multivariate analysis, CD59 percentage positivity was of independent prognostic significance with grade and lymph node stage. These findings indicate that loss of CD59 may offer a selective advantage for breast cancers, resulting in more aggressive tumours and conferring a poor prognosis for patients. Copyright © 2003 John Wiley & Sons, Ltd.Keywords
This publication has 26 references indexed in Scilit:
- Control of C3b and C5b deposition by CD46 (membrane cofactor protein) after alternative but not classical complement activationEuropean Journal of Immunology, 1999
- The complement regulatory proteins CD46 and CD59, but not CD55, are highly expressed by glandular epithelium of human breast and colorectal tumour tissuesAPMIS, 1998
- Tissue microarrays for high-throughput molecular profiling of tumor specimensNature Medicine, 1998
- High expression of the antigen recognized by the monoclonal antibody GB24 on human breast carcinomas: A preventive mechanism of malignant tumor cells against complement attack?Breast Cancer Research and Treatment, 1994
- The Nottingham prognostic index in primary breast cancerBreast Cancer Research and Treatment, 1992
- Overlapping but Nonidentical Binding Sites on CD2 for CD58 and a Second Ligand CD59Science, 1992
- GPI-Anchored Cell-Surface Molecules Complexed to Protein Tyrosine KinasesScience, 1991
- pathological prognostic factors in breast cancer. I. The value of histological grade in breast cancer: experience from a large study with long‐term follow‐upHistopathology, 1991
- Biology of complement: the overtureImmunology Today, 1991
- 20 KDa homologous restriction factor of complement resembles T cell activating proteinBiochemical and Biophysical Research Communications, 1989