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World J Biol Chem. Aug 26, 2013; 4(3): 64-70
Published online Aug 26, 2013. doi: 10.4331/wjbc.v4.i3.64
Autophagy and cancer
Si-Zhao Lu, Duygu Dee Harrison-Findik
Si-Zhao Lu, Department of Biochemistry and Molecular Biology, University of Nebraska Medical Center, Omaha, NE 68198, United States
Duygu Dee Harrison-Findik, Department of Internal Medicine, University of Nebraska Medical Center, Omaha, NE 68198, United States
Author contributions: Lu SZ and Harrison-Findik DD solely contributed to this paper.
Supported by Funding from the National Institutes of Health, No. R01 AA017738; University of Nebraska Medical Center Graduate Studies Research Fellowship
Correspondence to: Duygu Dee Harrison-Findik, PhD, Department of Internal Medicine, University of Nebraska Medical Center, 42nd and Emile Street, Omaha, NE 68198, United States. dharrisonfindik@unmc.edu
Telephone: +1-402-5596355 Fax: +1-402-5596494
Received: June 29, 2013
Revised: July 13, 2013
Accepted: July 17, 2013
Published online: August 26, 2013
Abstract

Autophagy is a homeostatic and evolutionarily conserved mechanism of self-digestion by which the cells degrade and recycle long-lived proteins and excess or damaged organelles. Autophagy is activated in response to both physiological and pathological stimuli including growth factor depletion, energy deficiency or the upregulation of Bcl-2 protein expression. A novel role of autophagy in various cancers has been proposed. Interestingly, evidence that supports both a positive and negative role of autophagy in the pathogenesis of cancer has been reported. As a tumor suppression mechanism, autophagy maintains genome stability, induces senescence and possibly autophagic cell death. On the other hand, autophagy participates in tumor growth and maintenance by supplying metabolic substrate, limiting oxidative stress, and maintaining cancer stem cell population. It has been proposed that the differential roles of autophagy in cancer are disease type and stage specific. In addition, substrate selectivity might be involved in carrying out the specific effect of autophagy in cancer, and represents one of the potential directions for future studies.

Keywords: Autophagy, Cancer, Cancer stem cells, Therapy resistance, Mitophagy, BNIP3

Core tip: The differential expression of selective autophagic receptors in cancers of different origin and stage might induce the selective removal or preservation of certain cellular components and contribute to either tumor suppression or cancer cell survival.