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Published on: October 11, 2012
Understanding autophagy in cell death control
Francesca Platini1, Ricardo Pérez-Tomás, Santiago Ambrosio
1Dept. of Food, Chemical, Pharmaceutical and Pharmacological Sciences (DISCAFF), University of East Piedmont A. Avogadro, Faculty of Pharmacy, Novara, Italy.
Abstract:
Autophagy is an evolutionarily conserved degradation pathway which primary functions as a cell survival adaptive mechanism during stress conditions. Autophagy is a tumor suppressor process and induction of the autophagic machinery can cause cell demise in apoptosis-resistant cancer. Thus, this metabolic pathway can act either to prevent or to promote carcinogenesis, as well as to modulate the response to anticancer therapies, included drug-induced apoptosis. Conventional therapies exert their cytotoxic activity mainly by inducing apoptosis. Massive activation of the apoptotic program in a tissue can result in cell loss providing a selective advantage for growth to displastic cells and tumor cell subpopulations with high levels of malignancy. This suggests that the activation of autophagy can counteract malignancy. On the contrary, therapeutic intervention-induced apoptosis can eliminate cells with pro-mutational biochemical alterations at risk for initiation, initiated cells and cells of focal and advanced preneoplastic and neoplastic lesions. Thus, pharmacological inhibition of autophagy may enhance apoptosis. Autophagy and apoptosis share common stimuli and signaling pathways, so that the final fate, life or death, depends on the cell response. Recently, accumulating data fuel novel potential therapeutic interventions to modulate autophagy to be beneficial in cancer therapy. This review highlights current knowledges aimed at unraveling the molecular interplay between autophagy and cell death as well as the possible therapeutic exploitation in cancer.
Insights
Autophagy, a cell survival process, can suppress tumors but also promote cancer. Modulating autophagy and apoptosis offers novel therapeutic strategies for cancer treatment.
Area of Science:
- Cellular Biology
- Molecular Oncology
- Cancer Therapeutics
Background:
- Autophagy is a conserved degradation pathway crucial for cell survival under stress.
- Autophagy exhibits dual roles in cancer, acting as both a tumor suppressor and promoter.
- Conventional cancer therapies primarily induce apoptosis for cytotoxic effects.
Purpose of the Study:
- To review the molecular interplay between autophagy and cell death (apoptosis) in cancer.
- To explore novel therapeutic strategies targeting autophagy modulation for cancer treatment.
- To understand how autophagy influences cancer development and response to therapy.
Main Methods:
- Literature review of current knowledge on autophagy and apoptosis in cancer.
- Analysis of signaling pathways shared by autophagy and apoptosis.
- Examination of therapeutic interventions modulating autophagy for cancer therapy.
Main Results:
- Autophagy induction can lead to cell death in apoptosis-resistant cancers, suggesting a tumor-suppressive role.
- Conversely, massive apoptosis induction by therapies can promote malignant cell growth.
- Pharmacological inhibition of autophagy may enhance apoptosis, offering a therapeutic avenue.
Conclusions:
- The balance between autophagy and apoptosis determines cell fate (survival or death) in cancer.
- Modulating autophagy presents promising therapeutic potential for enhancing cancer treatment efficacy.
- Further research into the complex interplay of autophagy and cell death is crucial for developing novel cancer therapies.
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