Journal
CELLS
Volume 11, Issue 9, Pages -Publisher
MDPI
DOI: 10.3390/cells11091479
Keywords
autophagy; apoptosis; cell signaling; lipid rafts; calcium; PINK1; cancer therapy
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Autophagy and apoptosis are two fundamental mechanisms regulating cell fate, and they are significantly interconnected through various crosstalk mechanisms. The crosstalk between autophagy and apoptosis impacts various pathologies, including rheumatic diseases. This Special Issue focuses on investigating the bioactive properties of antitumor drugs, particularly the role of anthraquinone derivatives in regulating cell death and autophagy crosstalk.
Autophagy and apoptosis represent two fundamental pathophysiological mechanisms of cell fate regulation. However, the signaling pathways of these processes are significantly interconnected through various mechanisms of crosstalk. Indeed, autophagy/apoptosis crosstalk is still an emerging field, in which an increasing number of molecules are involved, including, for example, PINK1 and ERLINs. On the other hand, this crosstalk involves signal transduction pathways which are strongly dependent on Ca2+. Interestingly, crosstalk between autophagy and apoptosis impacts several pathologies, including multiple rheumatic diseases. The purpose of this Special Issue is also to investigate the bioactive properties of drugs with antitumor activity, focusing particularly on the role of anthraquinone derivatives in the regulation of cell death and autophagy crosstalk. This Special Issue of Cells brings together the most recent advances in understanding the various aspects of crosstalk between autophagy and apoptosis and the interconnected signaling pathways, implying therapeutic perspectives for the utility of its modulation in an anti-cancer setting.
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