4.3 Article

PKCα-GSK3β-NF-κB signaling pathway and the possible involvement of TRIM21 in TRAIL-induced apoptosis

期刊

BIOCHEMISTRY AND CELL BIOLOGY
卷 94, 期 3, 页码 256-264

出版社

CANADIAN SCIENCE PUBLISHING, NRC RESEARCH PRESS
DOI: 10.1139/bcb-2016-0009

关键词

TRIM21; TRAIL; H1299 cells; GSK3 beta; PKC alpha

资金

  1. National Natural Science Foundation of China [31000628]
  2. National Program on Key Basic Research Project (973 Program) [2011CB910700]
  3. High-Level Talents Project of the Universities of Guangdong [[2011]431]
  4. Fundamental Research Funds for the Central Universities [21615407, 21609317]
  5. Science and Technology Program of Huadu District of Guangzhou, Guangdong Province [15-HDWS-016]

向作者/读者索取更多资源

Tumor necrosis factor related apoptosis-inducing ligand (TRAIL) is a highly promising therapeutic agent for cancer treatment, owing to its ability to selectively target tumor cells for cell death while having little effect on most normal cells. However, recent research has found that many cancers, including non-small cell lung cancer (NSCLC), display resistance to TRAIL. Therefore, it is important to elucidate the molecular mechanisms governing the resistance of tumor cells to TRAIL treatment. In this study, we show that GSK3 beta antagonized TRAIL-induced apoptosis in H1299 NSCLC cells, and determined that the PKC alpha isozyme is an upstream regulator of GSK3 beta that phosphorylates and inactivates GSK3 beta, thereby sensitizing cancer cells to TRAIL-induced apoptosis. Furthermore, we demonstrated that the anti-apoptotic effect of GSK3 beta is mediated by the NF-kappa B pathway, whereas the tripartite motif 21 (TRIM21) was able to inhibit the activation of NF-kappa B by GSK3 beta, and leads to the promotion of cell apoptosis. Taken together, our study further delineated the underpinning mechanism of resistance to TRAIL-induced apoptosis in H1299 cells, and provided new clues for sensitizing NSCLC cells to TRAIL therapy.

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