Expression of the glycosyl-phosphatidylinositol-anchored molecule-like prot
ein (GML) gene, a p53 target, correlates with the sensitivity of some cance
r cell lines to anticancer drugs and ionizing radiation. To investigate the
function of GML further, we introduced the GML cDNA into various cancer ce
ll lines under control of the tetracycline-regulated system. When we introd
uced GML into human glioblastoma cell line T98G, which lacks wild-type p53
and expresses no endogenous GML, we observed significant growth suppression
accompanied by G(2)/M arrest in two independent, stable cell lines. We con
firmed induction of apoptosis by fluorescence-activated cell sorting (FACS)
analysis and nuclear staining. Our results indicated that GML could induce
apoptosis of T98G without functional p53, and implied that GML plays a cru
cial role in the apoptotic pathway in some cancer cells.