Abstract

The downregulation of macroautophagy observed in cancer cells is associated with tumor progression. The regulation of macroautophagy by signaling pathways overlaps with the control of cell growth, proliferation, cell survival and death. Several tumor suppressor genes (PTEN, TSC2 and p53) involved in the mTOR signaling network have been shown to stimulate autophagy. In contrast, the oncoproteins involved in this network have the opposite effect. These findings, together with the discovery that haploinsufficiency of the tumor suppressor beclin 1 promotes tumorigenesis in various tissues in transgenic mice, give credibility to the idea that autophagy is a tumor suppressor mechanism. The induction of macroautophagy by cancer treatments may also contribute to cell eradication. However, cancer cells sometimes mobilize autophagic capacities in response to various stimuli without a fatal outcome, suggesting that they can also exploit macroautophagy for their own benefit.

Keywords

AutophagyBiologyPTENCarcinogenesisCell biologySuppressorCancer researchPI3K/AKT/mTOR pathwayCancerDownregulation and upregulationSignal transductionProgrammed cell deathTumor suppressor geneTumor progressionCancer cellApoptosisGeneGenetics

MeSH Terms

AnimalsApoptosis Regulatory ProteinsAutophagyBeclin-1Cell ProliferationCell SurvivalGenesTumor SuppressorHumansIntercellular Signaling Peptides and ProteinsMiceNeoplasmsOncogenesProtein KinasesProteinsSignal TransductionTOR Serine-Threonine Kinases

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Publication Info

Year
2006
Type
review
Volume
2
Issue
2
Pages
67-73
Citations
144
Access
Closed

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144
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Cite This

Joëlle Botti, Mojgan Djavaheri‐Mergny, Yannick Pilatte et al. (2006). Autophagy Signaling and the Cogwheels of Cancer. Autophagy , 2 (2) , 67-73. https://doi.org/10.4161/auto.2.2.2458

Identifiers

DOI
10.4161/auto.2.2.2458
PMID
16874041

Data Quality

Data completeness: 86%