Pathogenic Single Nucleotide Polymorphisms on Autophagy-Related Genes

• Published in: International journal of molecular sciences Vol. 21; no. 21; p. 8196
• Main Authors: Tamargo-Gómez, Isaac, Fernández, Álvaro F, Mariño, Guillermo
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI 02.11.2020; MDPI AG
• Subjects: Animals; ATGs; Autophagy; Autophagy-Related Protein 12 - genetics; Autophagy-Related Protein 5 - genetics; Autophagy-Related Protein 8 Family - genetics; Autophagy-Related Proteins - genetics; Cell Membrane - metabolism; Cytosol - metabolism; Humans; Immune System; Inflammation; Lysosomes - metabolism; pathology; Polymorphism, Single Nucleotide; polymorphisms; Prognosis; Protein Kinase C - genetics; Review; SNPs; variants; ATGs; autophagy; pathology; SNPs; autophagic receptors; lysosomes; variants; polymorphisms
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms21218196

In recent years, the study of single nucleotide polymorphisms (SNPs) has gained increasing importance in biomedical research, as they can either be at the molecular origin of a determined disorder or directly affect the efficiency of a given treatment. In this regard, sequence variations in genes involved in pro-survival cellular pathways are commonly associated with pathologies, as the alteration of these routes compromises cellular homeostasis. This is the case of autophagy, an evolutionarily conserved pathway that counteracts extracellular and intracellular stressors by mediating the turnover of cytosolic components through lysosomal degradation. Accordingly, autophagy dysregulation has been extensively described in a wide range of human pathologies, including cancer, neurodegeneration, or inflammatory alterations. Thus, it is not surprising that pathogenic gene variants in genes encoding crucial effectors of the autophagosome/lysosome axis are increasingly being identified. In this review, we present a comprehensive list of clinically relevant SNPs in autophagy-related genes, highlighting the scope and relevance of autophagy alterations in human disease.