Author/Authors :
Chen، نويسنده , , Kuo-Li and Chang، نويسنده , , Wun-Shaing Wayne and Cheung، نويسنده , , Chun Hei Antonio and Lin، نويسنده , , Chun-Cheng and Huang، نويسنده , , Chien-Chang and Yang، نويسنده , , Yung-Ning and Kuo، نويسنده , , Chang-Po and Kuo، نويسنده , , Ching-Chuan and Chang، نويسنده , , Yi-Hsun and Liu، نويسنده , , Ko-Jiunn and Wu، نويسنده , , Ching-Ming and Chang، نويسنده , , Jang-Yang، نويسنده ,
Abstract :
Cathepsin S is a cellular cysteine protease, which is frequently over-expressed in human cancer cells and plays important role in tumor metastasis. However, the role of cathepsin S in regulating cancer cell survival and death remains undefined. The aim of this study was to determine whether targeting cathepsin S could induce autophagy/apoptosis in cancer cells. In this study, we demonstrated that targeting cathepsin S by either specific small molecular inhibitors or cathepsin S siRNA induced autophagy and subsequent apoptosis in human cancer cells, and the induction of autophagy was dependent on the phosphorylation of EGFR and activation of the EGFR-related ERK/MAPK-signaling pathway. In conclusion, the current study reveals that cathepsin S plays an important role in the regulation of cell autophagy through interference with the EGFR–ERK/MAPK-signaling pathway.
Keywords :
EGFR , apoptosis , Cathepsin S , Autophagy , Erk