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Vanessa T. Blok, Mohamed R. Daha, Odette M. H. Tijsma, M. Geer Weissglas,
Lambert J. C. M. van den Broek, and Arko Gorter
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Departments
of Pathology (VTB, OMHT, LJCMB, AG), Nephrology (MRD), and Urology (MGW),
Leiden University Medical Center, Leiden, The Netherlands |
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SUMMARY: It is still unclear which membrane-bound regulatory proteins
(mCRP) are important in vivo to protect tumor cells from complement-mediated
damage. To address this question, the expression levels of CD46, CD55,
and CD59 were measured semi-quantitatively in situ on renal cell carcinomas
and compared with the expression level and cellular distribution of these
mCRP in proximal tubuli within each patient (n = 31). It was also
determined whether the expression of mCRP on tumor cells is associated
with deposition of C3d and C5b-9. CD46 expression was decreased on tumor
cells; in contrast, CD55 was expressed on tumor cells (12 out of 31 samples),
while it was not detected on proximal tubular epithelial cells (PTEC).
Also, expression of CD59 on tumor cells was increased as compared with
its expression on PTEC. Furthermore, the localization on the cell surface
of mCRP as observed on PTEC was altered on tumor cells. Because expression
of mCRP may limit a complement-mediated anti-tumor response, we determined
whether complement deposition was associated with the expression level
of CD46, CD55, and CD59. The presence of C3d on tumor cells was associated
with a low expression level of CD46 (p < 0.02). The expression
level of CD46 was also associated with a low tumor stage
(p < 0.04). The results suggest that in vivo CD46 plays a role
in the protection of human renal tumor cells from complement-mediated
injury. (Lab Invest 2000, 80: 345-357)
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