Results 41 to 50 of about 28,326 (246)
p62/SQSTM1 at the interface of aging, autophagy, and disease [PDF]
Advanced age is characterized by increased incidence of many chronic, noninfectious diseases that impair the quality of living of the elderly and pose a major burden on the healthcare systems of developed countries. These diseases are characterized by impaired or altered function at the tissue and cellular level, which is a hallmark of the aging ...
Alessandro, Bitto +5 more
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SQSTM1/p62: A Potential Target for Neurodegenerative Disease [PDF]
Neurodegenerative diseases, characterized by a progressive loss of brain function, affect the lives of millions of individuals worldwide. The complexity of the brain poses a challenge for scientists trying to map the biochemical and physiological pathways to identify areas of pathological errors.
Shifan Ma +2 more
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We provide evidence here from overexpression-based gain-of-function studies in human cells (1, 2) which demonstrate control of autophagy receptor p62/sequestosome 1 by the NLR (nucleotide-binding oligomerization domain-like receptor) family protein NOD2.
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Role of p62/SQSTM1 in liver physiology and pathogenesis [PDF]
p62/sequestosome-1/A170/ZIP (hereafter referred to as p62) is a scaffold protein that has multiple functions, such as signal transduction, cell proliferation, cell survival, cell death, inflammation, tumourigenesis and oxidative stress response. While p62 is an autophagy substrate and is degraded by autophagy, p62 serves as an autophagy receptor for ...
Sharon, Manley +2 more
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SQSTM1/p62 interacts with FKBP38 and regulates cell cycle in Cashmere goat foetal fibroblasts
SQSTM1 (sequestosome 1, also known as p62) is a multifunctional scaffold protein implicated in diverse cell physiology processes, such as autophagy, cell signalling, and protein turnover.
Qiburi He +9 more
doaj +1 more source
AbstractAutophagy is a highly conserved cellular process that allows degradation of large macromolecules. p62/SQSTM1 is a key adaptor protein that interacts both with material to be degraded and with LC3 at the autophagosome, enabling degradation of cargos such as protein aggregates, lipid droplets and damaged organelles by selective autophagy ...
Alcober‐Boquet, Lucia +12 more
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Mutations in the SQSTM1 gene have recently been identified as rare causes of progressive childhood neurodegenerative diseases. To date, only 27 cases have been reported, with 11 different mutations affecting SQSTM1.
Neda Hosseini Moshkenani +2 more
doaj +1 more source
p62/SQSTM1/A170: Physiology and pathology
p62/SQSTM1/A170 (hereafter referred to as p62) is a stress-inducible intracellular protein known to regulate various signal transduction pathways involved in cell survival and cell death. Comprehensive analysis of LC3 (an autophagosome localizing protein)-binding proteins resulted in the recognition of autophagy and p62.
Masaaki, Komatsu +2 more
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Synovitis is implicated in the pathology of osteoarthritis (OA) and significantly contributes to the development of OA. As a noninvasive physical therapy, low-intensity pulsed ultrasound (LIPUS) has been reported to possess anti-inflammatory effect in ...
Hangang Chen (757731) +9 more
core +1 more source
Functional CRISPR screening identifies the ufmylation pathway as a regulator of SQSTM1/p62
SQSTM1 is an adaptor protein that integrates multiple cellular signaling pathways and whose expression is tightly regulated at the transcriptional and post-translational level.
Rowena DeJesus +23 more
doaj +1 more source

