Objective. CD44 is a cell surface receptor implicated in tumor metastases.
We have previously shown that there is a loss of CD44 splice control in cle
ar cell carcinoma (CCCa) of the ovary. Our aim is to characterize the expre
ssion of CD44-3v, -5v, -7v, and -10v in clear cell ovarian tumors and to de
termine their prognostic value.
Methods. Twenty-two cases of ovarian CCCa were studied for CD44-3v, -5v, -7
v, and -10v expression by immunocytochemistry,
Results. The primary tumors showed expression of CD44-3v, -5v, -7v, and -10
v in 44, 55, 61, and 39% of the cases, respectively. We were able to compar
e the expression of CD44 in the primary tumor and metastatic sites from the
same patient in 7 cases (metastatic sites n 16). We observed decreased imm
unoreactivity of CD44-3v, -5v, -7v, and -10v in 67, 100, 93, and 92% of the
sites, respectively. CD44-3v and -10v expression was absent in 100% of the
nonaffected contralateral ovaries while -7v and -10v were expressed in 1/1
1 (9%) of them. When CD44-10v was not expressed in the primary tumor, only
18% of the women recurred or died of disease; in contrast, of the cases whe
re it was present, 71% of the women recurred or died of disease (P = 0.049)
.
Conclusions. There is aberrant alternative mRNA splicing in the development
of CCCa of the ovary when compared to the contralateral nonaffected ovary.
The expression of CD44-10v correlates with survival. Larger series are nee
ded to further understand the role of CD44 isoforms in ovarian cancer metas
tases. (C) 2000 Academic Press.