F. Carreiras et al., Human ovarian adenocarcinoma cells synthesize vitronectin and use it to organize their adhesion, GYNECOL ONC, 72(3), 1999, pp. 312-322
Extracellular matrix components and integrin receptors are frequently alter
ed in cancer, including ovarian adenocarcinoma. Vitronectin (Vn) is a matri
x protein mainly synthesized by liver cells; it is present in normal ovaria
n surface epithelium and differentiated ovarian adenocarcinoma, but is freq
uently undetectable in undifferentiated carcinoma (F. Carreiras et al., 199
6, Gynecol Oncol 62:260-267). Wondering about the cellular origin of Vn in
ovarian carcinoma, we searched for evidence of Vn synthesis by these tumors
. We demonstrated that three human ovarian adenocarcinoma cell lines were a
ble to synthesize Vn, as revealed by the presence of Vn mRNA and the protei
n. The Vn matrix promotes adhesion of ovarian tumor cells through Mi integr
ins. Moreover, during in vitro growth, Vn is progressively organized into a
particular pattern in combination with the recruitment of ay into focal co
ntacts. Our results suggest that Vn synthesis may participate in ovarian ad
enocarcinoma cell biology and raise the possibility that altered expression
of Vn in some ovarian carcinomas could result from a defect in Vn synthesi
s, (C) 1999 Academic Press.