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Showing papers by "Santiago Ambrosio published in 2010"


Journal ArticleDOI
TL;DR: Current knowledges aimed at unraveling the molecular interplay between autophagy and cell death as well as the possible therapeutic exploitation in cancer are highlighted.
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.

93 citations


Journal ArticleDOI
TL;DR: In this paper, the authors hypothesized that the aglycone of linamarin, acetone cyanohydrin, may be the cause of konzo, which is a neurotoxic motor disease caused by excess consumption of insufficiently processed cassava.

28 citations


Journal ArticleDOI
TL;DR: Evidence is presented that alpha-synuclein is highly expressed by sympathetic ganglion neurons throughout embryonic and postnatal life and that it is found in tyrosine hydroxylase-positive sympathetic fibers innervating the heart of adult mice, suggesting different actions of this molecule in central and peripheral catecholaminergic neurons.

10 citations


Journal ArticleDOI
TL;DR: In this article, a new line of α-synuclein (α-SYN) transgenic mice was generated in which the human wild-type α-SyN cDNA was expressed under the control of a tyrosine hydroxylase (TH) promoter.

9 citations