Abstract
Elongation factor-2 kinase (eEF-2 kinase; Ca2+/calmodulin- dependent kinase III) controls the rate of peptide chain elongation. The activity of eEF-2 kinase is increased in many malignancies, yet its precise function in carcinogenesis remains unknown. Autophagy, a well-defined survival pathway in yeast, may also play an important role in oncogenesis. Furthermore, the autophagic response to nutrient deprivation is regulated by the mammalian target of rapamycin (mTOR). eEF-2 kinase lies downstream of mTOR and is regulated by several kinases in this pathway. Therefore, we studied the role of eEF-2 kinase in autophagy. Knockdown of eEF-2 kinase by RNA interference inhibited autophagy in several cell types as measured by light chain 3 (LC3)-II formation, acidic vesicular organelle staining, and electron microscopy. In contrast, overexpression of eEF-2 kinase increased autophagy. Furthermore, inhibition of autophagy markedly decreased the viability of glioblastoma cells grown under conditions of nutrient depletion. These results suggest that eEF-2 kinase plays a regulatory role in the autophagic process in tumor cells and may promote cancer cell survival under conditions of nutrient deprivation. Therefore, eEF-2 kinase activation may be a part of a survival mechanism in glioblastoma, and targeting this kinase may represent a novel approach to cancer treatment.
Original language | English (US) |
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Pages (from-to) | 294-296 |
Number of pages | 3 |
Journal | Autophagy |
Volume | 2 |
Issue number | 4 |
DOIs | |
State | Published - 2006 |
All Science Journal Classification (ASJC) codes
- Molecular Biology
- Cell Biology
Keywords
- Autophagy
- Cancer
- Elongation factor-2 kinase
- Protein synthesis
- Survival pathway