Autophagic cell death: A new frontier in cancer research

HTML  XML Download Download as PDF (Size: 1294KB)  PP. 250-262  
DOI: 10.4236/abb.2013.42034    5,939 Downloads   10,310 Views  Citations

ABSTRACT

Autophagy is a conserved and tightly regulated cellular catabolic process that involves the lysosomal degradation pathway. Intracellular recycling of macromolecules and organelles provided by autophagy is an integral part of normal cellular function and permits cells survival under starvation conditions, maintaining cell growth and the homeostasis of organisms. In addition to its normal role in cell physiology, auto- phagy is closely linked to both tumorigenesis and cancer cell response to treatments. In fact, anticancer drugs can induce autophagy but it remains contro- versial whether this process leads to cancer cell death or protects cancer cells from cellular stress. The role of autophagy in cancer is complex and is likely dependent on tumor type, stage, and genetic context. However, recent evidences demonstrate a tight interconnection of autophagy with several cell death pathways and reveal an active contribution of auto- phagy to cell death. When autophagy is directly in- volved in the death process, the cell death process is designated “autophagic cell death” (ACD). In this review, we will give a comprehensive overview of the autophagic signaling pathway, its role and regulation in cancer cells; moreover, we will try to define the molecular mechanisms at the basis of the autophagic cell death showing that PPAR-γ activation plays a role in the induction of autophagy in cancer cells.

Share and Cite:

Zappavigna, S. , Luce, A. , Vitale, G. , Merola, N. , Facchini, S. and Caraglia, M. (2013) Autophagic cell death: A new frontier in cancer research. Advances in Bioscience and Biotechnology, 4, 250-262. doi: 10.4236/abb.2013.42034.

Copyright © 2024 by authors and Scientific Research Publishing Inc.

Creative Commons License

This work and the related PDF file are licensed under a Creative Commons Attribution 4.0 International License.