THE COMPLEMENT REGULATORY PROTEINS CD46 AND CD59, BUT NOT CD55, ARE HIGHLY EXPRESSED BY GLANDULAR EPITHELIUM OF HUMAN BREAST AND COLORECTALTUMOR-TISSUES
L. Thorsteinsson et al., THE COMPLEMENT REGULATORY PROTEINS CD46 AND CD59, BUT NOT CD55, ARE HIGHLY EXPRESSED BY GLANDULAR EPITHELIUM OF HUMAN BREAST AND COLORECTALTUMOR-TISSUES, APMIS. Acta pathologica, microbiologica et immunologica Scandinavica, 106(9), 1998, pp. 869-878
Three of the proteins protecting cells from autologous lysis by comple
ment are: membrane cofactor protein (MCP; CD46), an inhibitor of the m
embrane attack complex formation (CD59), and decay accelerating factor
(DAF; CD55). We have investigated the expression of these proteins in
breast and colorectal carcinoma by immunohistochemistry and immunoblo
tting of breast tissue for CD46. CD46 was consistently and strongly ex
pressed in the epithelial compartment in 26/28 ductal carcinomas of th
e breast, 9/9 fibroadenomas, and 9/11 cases of control non-neoplastic
breast tissue. CD59 showed a similar degree of expression in the fibro
adenomas (9/9), but was less strongly expressed in carcinomatous (22/2
8) and control (5/11) tissues. In marked contrast, no CD55 expression
was detected in tissue from 15 ductal carcinomas. Immunoblotting of br
east tissue for CD46 showed the same size of the molecule as for lymph
ocytes. It had however considerably stronger expression in tumour tiss
ue than in non-neoplastic tissue. CD46 and CD59 were either lacking or
only weakly expressed in the epithelial component of control colorect
al mucosa: 2/15 and 5/15, respectively. In contrast, tissue samples fr
om colorectal adenocarcinomas showed clear staining for both CD59 (10/
18) and, more markedly, CD46 (15/18). There was no association between
the pattern or intensity of CD46 and CD59 expression and tumour diffe
rentiation. As the complement regulatory proteins CD46 and CD59 are al
so strongly expressed by trophoblast at the fete-maternal tissue inter
face, these results support the concept that similar mechanisms are em
ployed both by the genetically dissimilar fetus and certain tumours to
evade immune attack by their host.