SQSTM1 Mutations and Glaucoma. [PDF]
Glaucoma is the most common cause of irreversible blindness worldwide. One subset of glaucoma, normal tension glaucoma (NTG) occurs in the absence of high intraocular pressure.
Todd E Scheetz +9 more
doaj +5 more sources
Association of p62/SQSTM1 excess and oral carcinogenesis. [PDF]
p62/SQSTM1 (sequestosome1) has never been evaluated in oral epithelium. In order to clarify the role of p62/SQSTM1 in carcinogenesis in oral epithelium, both p62/SQSTM1 and Nrf2 were immunohistochemically evaluated in 54 carcinomas and 14 low grade ...
Takuma Inui +5 more
doaj +5 more sources
SQSTM1/p62 as a therapeutic target in cancer
Cell survival depends on dynamic interactions among the signaling pathways that control the endoplasmic reticulum (ER) stress response, macroautophagy/autophagy and apoptotic cell death.
Hyeong-Reh C. Kim +3 more
doaj +4 more sources
Transformation of autophagic SQSTM1 droplets to SQSTM1-dependent P-bodies
SQSTM1/p62 droplets play crucial roles in droplets-based macroautophagy/autophagy including selective autophagy and bulk autophagy. We observed that under several stress milieus, SQSTM1 droplets entirely colocalize with P-body markers, and these stress-induced SQSTM1 droplets contain mRNAs.
Evelina Valionyte, Shouqing Luo
exaly +5 more sources
SQSTM1/p62 at the Crossroads of Autophagy, Inflammation, and Lethal Infection [PDF]
Sequestosome 1 (SQSTM1, also known as p62) has emerged as a multifunctional signaling adaptor that bridges autophagy, proteostasis, and inflammation. In this review, we discuss the molecular mechanisms by which SQSTM1 regulates selective autophagy and ...
Ruoxi Zhang, Rui Kang, Daolin Tang
doaj +2 more sources
The lysine methyltransferase KMT5a and p53 regulate the expression of the key autophagy adaptor p62/SQSTM1 in glioblastoma [PDF]
Background KMT5a, a histone lysine methyltransferase responsible for histone H4 lysine 20 monomethylation (H4K20me1), plays a critical role in the pathogenesis of various human diseases, including cancer.
Rosa Della Monica +19 more
doaj +2 more sources
Novel SQSTM1 (c.838G>T) Mutation Identified in Two Unrelated Cases of Cerebellar Ataxia and Gaze Palsy [PDF]
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 +2 more sources
YTHDC1 modulates the malignant phenotype of retinoblastoma via SQSTM1-mediated autophagy [PDF]
Retinoblastoma (RB) is the most common pediatric intraocular malignancy, yet the role of N6-methyladenosine (m6A) regulators in RB progression remains unclear.
Jie Ding +5 more
doaj +2 more sources
Association between SQSTM1 dysregulation and risk in alopecia areata: a Mendelian randomization study [PDF]
BackgroundAlopecia areata (AA) is an autoimmune disease typified by nonscarring hair loss. It manifests as a heterogeneous disorder with diverse clinical presentations and variable treatment responses, underscoring the significance of identifying novel ...
Lifang Hu, Sheng Wan, Xiuzu Song
doaj +2 more sources
Extracellular SQSTM1 as an inflammatory mediator [PDF]
Excessive inflammation may lead to irreparable injury and even death, but the key mediators and underlying mechanisms remain unclear. Our recent findings indicate that SQSTM1/p62 (sequestosome 1), a well-known macroautophagy/autophagy receptor, is a lethal inflammatory mediator of sepsis and septic shock.
Borong Zou +4 more
openaire +2 more sources

