Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2006 Aug;55(8):973-80.
doi: 10.1007/s00262-005-0055-0. Epub 2005 Sep 3.

Expression of the membrane complement regulatory protein CD59 (protectin) is associated with reduced survival in colorectal cancer patients

Affiliations

Expression of the membrane complement regulatory protein CD59 (protectin) is associated with reduced survival in colorectal cancer patients

Nicholas F S Watson et al. Cancer Immunol Immunother. 2006 Aug.

Abstract

It has been known for some time that the immune system can recognise growing tumours, and that tumours may respond by modulation of molecules, which make them resistant to further attack. Expression, over-expression, or loss of these molecules may function as markers of tumour progression and prognosis. Among such molecules are the membrane-bound complement regulatory proteins (mCRP), which protect cells from bystander attack by autologous complement. These include CD59 (protectin), which prevents formation of the MAC complex in the terminal stages of complement activation. In the present study, we evaluated immunohistochemical expression of CD59 in a series of over 460 well-characterised colorectal cancers using tissue microarrays (TMA), and related this information to known tumour and patient variables and to survival. The CD59 expression was observed in 69 (15%) of cases overall, and was significantly associated with tumour grade. In contrast, no associations were noted with tumour site, stage or histological type. On survival analysis, a further correlation was observed between expression of CD59 by the colorectal tumours and a reduction in disease-specific patient survival. This observation was strongest for patients with early stage disease. However, a negative impact on survival was also seen in those patients with late stage disease. These results indicate that TMA linked to good clinicopathological databases with good long term follow up are useful tools for determining new prognostic indicators that can be used in future patient management. Immune surveillance may result in immune-editing that induces variable expression of a range of target antigens, and these may be useful prognostic markers. This study has identified CD59 expression as a marker of poor prognosis in colorectal cancer patients.

PubMed Disclaimer

Figures

Fig. 1
Fig. 1
a Colorectal TMA core stained with anti-CD59 antibody (1:10 dilution) demonstrating positive CD59 expression in tumour cell cytoplasm and at luminal membrane. b Colorectal TMA core from the same slide with absent tumour expression of CD59. Note strongly positive staining of vascular endothelial cells acting as internal positive control (both at 20 times original magnification)
Fig. 2
Fig. 2
a Kaplan–Meier plot for all patients showing disease-specific survival for CD59 positive/negative tumours (n=449). b Kaplan–Meier plot for TNM stage 0/I/II patients (n=242). c Kaplan–Meier plot for TNM stage III/IV patients (n=207)

Similar articles

Cited by

References

    1. Bjorge L, Jensen TS, Matre R. Characterisation of the complement-regulatory proteins decay accelerating factor (DAF, CD55) and membrane cofactor protein (MCP, CD46) on a human colonic adenocarcinoma cell line. Cancer Immunol Immunother. 1996;42:185–192. doi: 10.1007/s002620050269. - DOI - PMC - PubMed
    1. Bjorge L, Vedeler CA, Ulvestad E, Matre R. Expression and function of CD59 on colonic adenocarcinoma cells. Eur J Immunol. 1994;24:1597–1603. doi: 10.1002/eji.1830240722. - DOI - PubMed
    1. Camp RL, Charette LA, Rimm DL. Validation of tissue microarray technology in breast carcinoma. Lab Invest. 2000;80:1943–1949. - PubMed
    1. Donin N, Jurianz K, Ziporen L, Schultz S, Kirschfink M, Fishelson Z. Complement resistance of human cells depends on membrane regulatory proteins, protein kinases and sialic acid. Clin Exp Immunol. 2003;131:254–263. doi: 10.1046/j.1365-2249.2003.02066.x. - DOI - PMC - PubMed
    1. Dunn GP, Old LJ, Schreiber RD. The three Es of cancer immunoediting. Ann Rev Immunol. 2004;22:329–360. doi: 10.1146/annurev.immunol.22.012703.104803. - DOI - PubMed