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Targeting cathepsin S induces tumor cell autophagy via the EGFR-ERK signaling pathway
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Targeting cathepsin S induces tumor cell autophagy via the EGFR-ERK signaling pathway

Kuo-Li Chen, Wun-Shaing Wayne Chang, Chun Hei Antonio Cheung, Chun-Cheng Lin, Chien-Chang Huang, Yung-Ning Yang, Chang-Po Kuo, Ching-Chuan Kuo, Yi-Hsun Chang, Ko-Jiunn Liu, …
Cancer Letters, 卷.317(1), 頁碼.89-98
04/2012
PMID: 22101325

摘要

Apoptosis Autophagy Cathepsin S EGFR ERK Cancer Research Oncology
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. © 2011 Elsevier Ireland Ltd.

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