Author/Authors :
Lee، نويسنده , , Jeng-Woei and Lee، نويسنده , , Kuei-Fang and Hsu، نويسنده , , Hsue-Yin and Hsu، نويسنده , , Lee-Ping and Shih، نويسنده , , Wen-Ling and Chu، نويسنده , , Yi-Chih and Hsiao، نويسنده , , Weiting and Liu، نويسنده , , Po-Fan Chen، نويسنده ,
Abstract :
Prostate apoptosis response-4 (Par-4) is a proapoptotic gene that selectively induces cell death in most cancer cells. In addition to the increased percentage of apoptotic cells, caspase-3 activity, and poly (ADP-ribose) polymerase (PARP) cleavage, we demonstrate that elevated expression of Par-4 and nuclear entry resulted in apoptosis of nasopharyngeal carcinoma (NPC) cell lines either in serum deprivation or by ectopic overexpression of Par-4. Moreover, disassociation from the Par-4/Akt complex was correlated with the induced proapoptotic ability of Par-4. Therefore, our data suggest that the cytoplasmic localization and expression level of endogenous Par-4 in NPC cells are not sufficient to augment apoptosis.