Journal
CANCER CELL
Volume 38, Issue 2, Pages 247-+Publisher
CELL PRESS
DOI: 10.1016/j.ccell.2020.05.018
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Funding
- NCI
- NIDDK of the NIH [R01DK108743, R01CA211794, R01CA218254, CA211794, CA234128, R01CA234245]
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Oxidative stress plays a critical role in liver tissue damage and in hepatocellular carcinoma (HCC) initiation and progression. However, the mechanisms that regulate autophagy and metabolic reprogramming during reactive oxygen species (ROS) generation, and how ROS promote tumorigenesis, still need to be fully understood. We show that protein kinase C (PKC) lambda/iota loss in hepatocytes promotes autophagy and oxidative phosphorylation. This results in ROS generation, which through NRF2 drives HCC through cell-autonomous and non-autonomous mechanisms. Although PKC lambda/iota promotes tumorigenesis in oncogene-driven cancer models, emerging evidence demonstrate that it is a tumor suppressor in more complex carcinogenic processes. Consistently, PKC lambda/iota levels negatively correlate with HCC histological tumor grade, establishing this kinase as a tumor suppressor in liver cancer.
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