NF-κB-mediated repression of growth arrest- and DNA-damage-inducible proteins 45α and γ is essential for cancer cell survival
NF-κB-mediated repression of growth arrest- and DNA-damage-inducible proteins 45α and γ is essential for cancer cell survival
The NF-κB/IκB signaling pathway is a critical regulator of cell survival in cancer. Here, we report that combined down-regulation of growth arrest- and DNA-damage-inducible proteins (GADD)45α and γ expression by NF-κB is an essential step for various cancer types to escape programmed cell death. We demonstrate that inhibition of NF-κB in cancer cells results in GADD45α- and γ-dependent induction of apoptosis and inhibition of tumor growth. Inhibition of GADD45α and γ in cancer cells by small interfering RNA abrogates apoptosis induction by the inhibitor of NF-κB and blocks c-Jun N-terminal kinase activation, whereas overexpression of GADD45α and γ activates c-Jun N-terminal kinase and induces apoptosis. These results establish an unambiguous role for the GADD45 family as an essential mediator of cell survival in cancer cells with implications for cancer chemotherapy and novel drug discovery.
- Beth Israel Deaconess Medical Center United States
- Salk Institute for Biological Studies United States
GADD45 Proteins, Cell Survival, Intracellular Signaling Peptides and Proteins, JNK Mitogen-Activated Protein Kinases, NF-kappa B, Proteins, Apoptosis, Enzyme Activation, Gene Expression Regulation, Neoplastic, Proto-Oncogene Proteins c-myc, Mice, Cell Line, Tumor, Neoplasms, Animals, Humans, I-kappa B Proteins, Mitogen-Activated Protein Kinases, Cell Division, DNA Damage, Signal Transduction
GADD45 Proteins, Cell Survival, Intracellular Signaling Peptides and Proteins, JNK Mitogen-Activated Protein Kinases, NF-kappa B, Proteins, Apoptosis, Enzyme Activation, Gene Expression Regulation, Neoplastic, Proto-Oncogene Proteins c-myc, Mice, Cell Line, Tumor, Neoplasms, Animals, Humans, I-kappa B Proteins, Mitogen-Activated Protein Kinases, Cell Division, DNA Damage, Signal Transduction
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