The majority of ovarian cancers are derived from ovarian surface epithelial
cells that are sequestered in inclusion cysts within the ovarian stroma. W
e propose that the Fas/Fas ligand system is responsible for the normal elim
ination of these inclusion cysts through apoptosis, thereby removing potent
ial sites of ovarian tumors. Furthermore, we hypothesize that the failure o
f the Fas/Fas ligand's apoptotic signaling mechanism leads to the persisten
ce of these inclusion cysts in the stroma, and the onset of ovarian tumorig
enesis.