| Literature DB >> 33975805 |
Amer Jamalpoor1, Amr Othman1, Elena N Levtchenko2, Rosalinde Masereeuw3, Manoe J Janssen4.
Abstract
Nephropathic cystinosis is a severe, monogenic systemic disorder that presents early in life and leads to progressive organ damage, particularly affecting the kidneys. It is caused by mutations in the CTNS gene, which encodes the lysosomal transporter cystinosin, resulting in intralysosomal accumulation of cystine. Recent studies demonstrated that the loss of cystinosin is associated with disrupted autophagy dynamics, accumulation of distorted mitochondria, and increased oxidative stress, leading to abnormal proliferation and dysfunction of kidney cells. We discuss these molecular mechanisms driving nephropathic cystinosis. Further, we consider how unravelling molecular mechanisms supports the identification and development of new strategies for cystinosis by the use of small molecules, biologicals, and genetic rescue of the disease in vitro and in vivo.Entities:
Keywords: CTNS gene; cystinosis; lysosomal storage disorder; renal Fanconi syndrome; therapeutic strategies
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Year: 2021 PMID: 33975805 DOI: 10.1016/j.molmed.2021.04.004
Source DB: PubMed Journal: Trends Mol Med ISSN: 1471-4914 Impact factor: 11.951