Abstract

The lysosomal degradation pathway of autophagy plays a fundamental role in cellular, tissue, and organismal homeostasis and is mediated by evolutionarily conserved autophagy-related (ATG) genes. Definitive etiological links exist between mutations in genes that control autophagy and human disease, especially neurodegenerative, inflammatory disorders and cancer. Autophagy selectively targets dysfunctional organelles, intracellular microbes, and pathogenic proteins, and deficiencies in these processes may lead to disease. Moreover, ATG genes have diverse physiologically important roles in other membrane-trafficking and signaling pathways. This Review discusses the biological functions of autophagy genes from the perspective of understanding-and potentially reversing-the pathophysiology of human disease and aging.

Keywords

BiologyAutophagyGenePerspective (graphical)DiseaseGeneticsComputational biologyCell biologyApoptosis

MeSH Terms

AnimalsAutophagyAutophagy-Related ProteinsHomeostasisHumansLysosomesNeurodegenerative DiseasesProteinsSignal Transduction

Affiliated Institutions

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Publication Info

Year
2019
Type
review
Volume
176
Issue
1-2
Pages
11-42
Citations
2632
Access
Closed

Social Impact

Social media, news, blog, policy document mentions

Citation Metrics

2632
OpenAlex
45
Influential
2355
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Cite This

Beth Levine, Guido Kroemer (2019). Biological Functions of Autophagy Genes: A Disease Perspective. Cell , 176 (1-2) , 11-42. https://doi.org/10.1016/j.cell.2018.09.048

Identifiers

DOI
10.1016/j.cell.2018.09.048
PMID
30633901
PMCID
PMC6347410

Data Quality

Data completeness: 90%