Upregulation of Beclin-1 expression and phosphorylation of Bcl-2 and p53 are involved in the JNK-mediated autophagic cell death

• Published in: Biochemical and biophysical research communications Vol. 382; no. 4; pp. 726 - 729
• Main Authors: Park, Kyung-Jin, Lee, Seung-Hyun, Lee, Chang-Han, Jang, Ji-Young, Chung, Junho, Kwon, Myung-Hee, Kim, Yong-Sung
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 15.05.2009
• Subjects: Apoptosis Regulatory Proteins - biosynthesis; Autophagic cell death; Autophagy; Bcl-2 phosphorylation; Beclin-1; Beclin-1 upregulation; Cell Line, Tumor; Humans; JNK activation; JNK Mitogen-Activated Protein Kinases - metabolism; Membrane Proteins - biosynthesis; p53 phosphorylation; Phosphorylation; Proto-Oncogene Proteins c-bcl-2 - metabolism; Receptors, TNF-Related Apoptosis-Inducing Ligand - agonists; Tumor Suppressor Protein p53 - metabolism; Up-Regulation; Autophagic cell death; Bcl-2 phosphorylation; JNK activation; Beclin-1 upregulation; p53 phosphorylation
• ISSN: 0006-291X; 1090-2104
• DOI: 10.1016/j.bbrc.2009.03.095

Though the activation of c-Jun NH2-terminal kinase (JNK) has been reported to be essential for autophagic cell death in response to various stressors, the molecular links between JNK activation and autophagic cell death signaling remain elusive. Here we report that, in the JNK-dependent autophagic cell death of HCT116 cells induced by an agonistic single chain variable fragment antibody, HW1, against human death receptor 5 (DR5), JNK activation upregulated Beclin-1 expression and induced Bcl-2 and p53 phosphorylation. Further, the p53-deficient HCT116 cells showed less susceptibility to the HW1-mediated autophagic cell death than the wild type cells, suggesting that JNK-mediated p53 phosphorylation promotes the autophagic cell death. Our results suggest that DR5-stimulated JNK activation and its consequent fluxes into the pro-autophagic signaling pathways contribute to the autophagic cell death in cancer cells.