A Comprehensive Review of Autophagy and Its Various Roles in Infectious, Non-Infectious, and Lifestyle Diseases: Current Knowledge and Prospects for Disease Prevention, Novel Drug Design, and Therapy.
Rekha KhandiaMaryam DadarAshok MunjalKuldeep DhamaKumaragurubaran KarthikRuchi TiwariMohammad Iqbal YatooHafiz M N IqbalKaram Pal SinghSunil K JoshiWanpen ChaicumpaPublished in: Cells (2019)
Autophagy (self-eating) is a conserved cellular degradation process that plays important roles in maintaining homeostasis and preventing nutritional, metabolic, and infection-mediated stresses. Autophagy dysfunction can have various pathological consequences, including tumor progression, pathogen hyper-virulence, and neurodegeneration. This review describes the mechanisms of autophagy and its associations with other cell death mechanisms, including apoptosis, necrosis, necroptosis, and autosis. Autophagy has both positive and negative roles in infection, cancer, neural development, metabolism, cardiovascular health, immunity, and iron homeostasis. Genetic defects in autophagy can have pathological consequences, such as static childhood encephalopathy with neurodegeneration in adulthood, Crohn's disease, hereditary spastic paraparesis, Danon disease, X-linked myopathy with excessive autophagy, and sporadic inclusion body myositis. Further studies on the process of autophagy in different microbial infections could help to design and develop novel therapeutic strategies against important pathogenic microbes. This review on the progress and prospects of autophagy research describes various activators and suppressors, which could be used to design novel intervention strategies against numerous diseases and develop therapeutic drugs to protect human and animal health.
Keyphrases
- cell death
- endoplasmic reticulum stress
- oxidative stress
- signaling pathway
- cell cycle arrest
- randomized controlled trial
- healthcare
- public health
- metabolic syndrome
- late onset
- pseudomonas aeruginosa
- weight loss
- physical activity
- stem cells
- cardiovascular disease
- social media
- mesenchymal stem cells
- transcription factor
- cystic fibrosis
- copy number
- poor prognosis
- dna methylation
- weight gain
- induced pluripotent stem cells
- duchenne muscular dystrophy