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Cited by 155 publications
(135 citation statements)
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“…The ultimate cancer risk factor is old age, which has a detrimental effect on autophagy (Martinez-Lopez et al, 2015). Defective autophagy in aged individuals or animals results in aberrant clearance of damaged mitochondria, leading to elevated inflammation and accumulation of ROS and protein aggregates that cause ER stress (Bujak et al, 2015; Komatsu et al, 2006).…”
Section: Corruption Of Autophagy By Cancer Risk Factorsmentioning
confidence: 99%
See 1 more Smart Citation
“…The ultimate cancer risk factor is old age, which has a detrimental effect on autophagy (Martinez-Lopez et al, 2015). Defective autophagy in aged individuals or animals results in aberrant clearance of damaged mitochondria, leading to elevated inflammation and accumulation of ROS and protein aggregates that cause ER stress (Bujak et al, 2015; Komatsu et al, 2006).…”
Section: Corruption Of Autophagy By Cancer Risk Factorsmentioning
confidence: 99%
“…Defective autophagy in aged individuals or animals results in aberrant clearance of damaged mitochondria, leading to elevated inflammation and accumulation of ROS and protein aggregates that cause ER stress (Bujak et al, 2015; Komatsu et al, 2006). These cellular defects contribute to different degenerative diseases and enhance tumor initiation and malignant progression (Martinez-Lopez et al, 2015). Aging is accompanied by indolent inflammation and parainflammation manifested by increased basal production of IL-1β, IL-18, TNF and IL-6.…”
Section: Corruption Of Autophagy By Cancer Risk Factorsmentioning
confidence: 99%
“…Both apoptosis and autophagy possibly contribute to age-related sarcopenia that is associated with loss in the overall mass and with a reduced number of myofibers. 14,[21][22][23][24][25] Disorganization of myofibrils with Z line loss, mitochondrial swelling and sarcolemmal disruption are hallmarks of the skeletal muscle necrosis. Intracellular moieties including myoglobin, creatine phosphokinase (CK) and other sarcoplasm proteins are released into the bloodstream.…”
Section: Unique Immune Privileges Of the Skeletal Musclementioning
confidence: 99%
“…There, lysosome-associated protein type 2A (LAMP-2A) is recognized by this substrate chaperone complex, allowing the target protein to unfold and cross the lysosomal membrane. CMA is thus characterized by selective protein targeting and direct substrate translocation to the lysosomes, which establishes a singular role of this process in diverse pathophysiological conditions, including aging (Cuervo, 2011; Dice, 2007; Martinez-Lopez et al, 2015)(see also this issue). Instead, microautophagy involves the direct invagination of cytosolic material (‘in bulk’ or selectively chosen by chaperones) at the lysosomal membrane (Li et al, 2012).…”
Section: Lysosomes and The Regulation Of Autophagy During Agingmentioning
confidence: 99%