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Farnesyltransferase inhibition in HGPS.
Misteli, Tom.
Afiliação
  • Misteli T; National Cancer Institute, NIH, Bethesda, MD, USA. Electronic address: tom.misteli@nih.gov.
Cell ; 184(2): 293, 2021 01 21.
Article em En | MEDLINE | ID: mdl-33482093
ABSTRACT
The ultra-rare, pediatric premature aging disorder Hutchinson-Gilford progeria syndrome (HGPS) is caused by mutation of LMNA, encoding the nuclear architectural protein lamin A. Patients develop atherosclerosis and typically die of heart failure in their teens. FDA-approved Zokinvy prevents farnesylation of lamin A, reduces vascular stiffness, and extends survival in HGPS patients. To view this Bench to Bedside, open or download the PDF.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Progéria / Inibidores Enzimáticos / Farnesiltranstransferase Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Progéria / Inibidores Enzimáticos / Farnesiltranstransferase Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article