The aim of this study was to investigate the expression of Fas and Fas liga
nd (FasL) and to determine the significance of these molecules in lung canc
er cell lines. Immunoblotting, RT-PCR and flow cytometric analyses were car
ried out to measure the expression of Fas and Fast and to examine their int
eractions and effects on cell growth and apoptosis. Fas and Fast were coexp
ressed in most of the cell lines but to varying degrees. Apoptosis induced
by the agonistic anti-Fas antibody was significantly correlated with Fas ex
pression (P = 0.0075), whereas cisplatin-induced apoptosis was not. Upregul
ation of Fas and Fast expression by the administration of cisplatin was fou
nd in 7 of 11 (64%) and 9 of 11 (82%) cell lines, respectively. However, ci
splatin-induced apoptosis was not suppressed by antagonistic anti-Fast anti
body. Thus, our data indicated that Fas and Fast were co-expressed in lung
cancer cell lines, and that Fas ligation induced by agonistic anti-Fas anti
body is functional and induced apoptosis that was dependent on the levels o
f Fas expression. In contrast, Fas-FasL interactions appeared to be non-fun
ctional. Furthermore, our results suggest that cisplatin-induced apoptosis
in lung cancer cells was independent of the Fas-Fast interaction. (C) 2000
Elsevier Science Ltd. All rights reserved.