Autophagy, a key mechanism of oncogenesis and resistance in leukemia

P Auberger, A Puissant - Blood, The Journal of the American …, 2017 - ashpublications.org
Autophagy is a lysosomal pathway involved in degradation of intracellular material. It
appears as an adaptation mechanism that is essential for cellular homeostasis in response …

Stress granules at the intersection of autophagy and ALS

Z Monahan, F Shewmaker, UB Pandey - Brain research, 2016 - Elsevier
Amyotrophic lateral sclerosis (ALS) is a progressive, fatal disease caused by loss of upper
and lower motor neurons. The majority of ALS cases are classified as sporadic (80–90%) …

Age-dependent accumulation of oligomeric SNCA/α-synuclein from impaired degradation in mutant LRRK2 knockin mouse model of Parkinson disease: role for …

PWL Ho, CT Leung, H Liu, SYY Pang, CSC Lam… - Autophagy, 2020 - Taylor & Francis
Parkinson disease (PD) is an age-related neurodegenerative disorder associated with
misfolded SNCA/α-synuclein accumulation in brain. Impaired catabolism of SNCA …

Chemical modulation of chaperone-mediated autophagy by retinoic acid derivatives

J Anguiano, TP Garner, M Mahalingam, BC Das… - Nature chemical …, 2013 - nature.com
Chaperone-mediated autophagy (CMA) contributes to cellular quality control and the
cellular response to stress through the selective degradation of cytosolic proteins in …

[HTML][HTML] All-trans retinoic acid and rapamycin normalize Hutchinson Gilford progeria fibroblast phenotype

C Pellegrini, M Columbaro, C Capanni, MR D'Apice… - Oncotarget, 2015 - ncbi.nlm.nih.gov
Hutchinson Gilford progeria syndrome is a fatal disorder characterized by accelerated aging,
bone resorption and atherosclerosis, caused by a LMNA mutation which produces progerin …

Chaperone‐mediated autophagy: Molecular mechanisms, biological functions, and diseases

R Yao, J Shen - MedComm, 2023 - Wiley Online Library
Chaperone‐mediated autophagy (CMA) is a lysosomal degradation pathway that eliminates
substrate proteins through heat‐shock cognate protein 70 recognition and lysosome …

Neuroprotective Effect of Bexarotene in the SOD1G93A Mouse Model of Amyotrophic Lateral Sclerosis

J Riancho, M Ruiz-Soto, MT Berciano… - Frontiers in cellular …, 2015 - frontiersin.org
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by
progressive weakness and muscle atrophy related to the loss of upper and lower motor …

All‐trans retinoic acid (ATRA)‐induced TFEB expression is required for myeloid differentiation in acute promyelocytic leukemia (APL)

N Orfali, TR O'Donovan, MR Cahill… - European journal of …, 2020 - Wiley Online Library
Objective In acute promyelocytic leukemia (APL), normal retinoid signaling is disrupted by
an abnormal PML‐RARα fusion oncoprotein, leading to a block in cell differentiation …

Retinoic acid receptor-targeted drugs in neurodegenerative disease

JN Clark, A Whiting, P McCaffery - Expert Opinion on Drug …, 2020 - Taylor & Francis
Introduction Neurodegenerative diseases including amyotrophic lateral sclerosis (ALS),
Alzheimer's disease (AD) and Parkinson's disease (PD) are characterized by progressive …

Kansl1 haploinsufficiency impairs autophagosome-lysosome fusion and links autophagic dysfunction with Koolen-de Vries syndrome in mice

T Li, D Lu, C Yao, T Li, H Dong, Z Li, G Xu… - Nature …, 2022 - nature.com
Abstract Koolen-de Vries syndrome (KdVS) is a rare disorder caused by haploinsufficiency
of KAT8 regulatory NSL complex subunit 1 (KANSL1), which is characterized by intellectual …