National Institute of Cancer Research, National Health Research Institutes, Tainan, Taiwan, ROC.
Cancer Lett. 2012 Apr 1;317(1):89-98. doi: 10.1016/j.canlet.2011.11.015. Epub 2011 Nov 18.
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.
组织蛋白酶 S 是一种细胞半胱氨酸蛋白酶,在人类癌细胞中经常过度表达,在肿瘤转移中发挥重要作用。然而,组织蛋白酶 S 在调节癌细胞存活和死亡中的作用尚不清楚。本研究旨在确定靶向组织蛋白酶 S 是否可以诱导癌细胞发生自噬/凋亡。在这项研究中,我们证明了通过特异性小分子抑制剂或组织蛋白酶 S siRNA 靶向组织蛋白酶 S 可诱导人癌细胞发生自噬和随后的凋亡,并且自噬的诱导依赖于 EGFR 的磷酸化和 EGFR 相关的 ERK/MAPK 信号通路的激活。总之,本研究揭示了组织蛋白酶 S 通过干扰 EGFR-ERK/MAPK 信号通路在细胞自噬的调节中发挥重要作用。