TY - JOUR
T1 - Biological Functions of Autophagy Genes
T2 - A Disease Perspective
AU - Levine, Beth
AU - Kroemer, Guido
N1 - Publisher Copyright:
© 2018 Elsevier Inc.
PY - 2019/1/10
Y1 - 2019/1/10
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85059392998&partnerID=8YFLogxK
U2 - 10.1016/j.cell.2018.09.048
DO - 10.1016/j.cell.2018.09.048
M3 - Review article
C2 - 30633901
AN - SCOPUS:85059392998
SN - 0092-8674
VL - 176
SP - 11
EP - 42
JO - Cell
JF - Cell
IS - 1-2
ER -