Literature DB >> 28086161

A-type lamins and cardiovascular disease in premature aging syndromes.

Beatriz Dorado1, Vicente Andrés2.   

Abstract

Lamin A is a nuclear intermediate filament protein with important structural and regulatory roles in most differentiated mammalian cells. Excessive accumulation of its precursor prelamin A or the mutant form called 'progerin' causes premature aging syndromes. Progeroid 'laminopathies' are characterized by severe cardiovascular problems (cardiac electrical defects, vascular calcification and stiffening, atherosclerosis, myocardial infarction, and stroke) and premature death. Here, we review studies in cell and mouse models and patients that are unraveling how abnormal prelamin A and progerin accumulation accelerates cardiovascular disease and aging. This knowledge is essential for developing effective therapies to treat progeria and may help identify new mechanisms underlying normal aging.
Copyright © 2016 Elsevier Ltd. All rights reserved.

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Year:  2017        PMID: 28086161     DOI: 10.1016/j.ceb.2016.12.005

Source DB:  PubMed          Journal:  Curr Opin Cell Biol        ISSN: 0955-0674            Impact factor:   8.382


  18 in total

1.  DNA Damage Response/TP53 Pathway Is Activated and Contributes to the Pathogenesis of Dilated Cardiomyopathy Associated With LMNA (Lamin A/C) Mutations.

Authors:  Suet Nee Chen; Raffaella Lombardi; Jennifer Karmouch; Ju-Yun Tsai; Grace Czernuszewicz; Matthew R G Taylor; Luisa Mestroni; Cristian Coarfa; Priyatansh Gurha; Ali J Marian
Journal:  Circ Res       Date:  2019-03-15       Impact factor: 17.367

Review 2.  Telomeres and telomerase: three decades of progress.

Authors:  Jerry W Shay; Woodring E Wright
Journal:  Nat Rev Genet       Date:  2019-05       Impact factor: 53.242

Review 3.  Small-Molecule Therapeutic Perspectives for the Treatment of Progeria.

Authors:  Jon Macicior; Beatriz Marcos-Ramiro; Silvia Ortega-Gutiérrez
Journal:  Int J Mol Sci       Date:  2021-07-03       Impact factor: 5.923

4.  ZMPSTE24 missense mutations that cause progeroid diseases decrease prelamin A cleavage activity and/or protein stability.

Authors:  Eric D Spear; Erh-Ting Hsu; Laiyin Nie; Elisabeth P Carpenter; Christine A Hrycyna; Susan Michaelis
Journal:  Dis Model Mech       Date:  2018-07-13       Impact factor: 5.758

5.  Progerin accelerates atherosclerosis by inducing endoplasmic reticulum stress in vascular smooth muscle cells.

Authors:  Magda R Hamczyk; Ricardo Villa-Bellosta; Víctor Quesada; Pilar Gonzalo; Sandra Vidak; Rosa M Nevado; María J Andrés-Manzano; Tom Misteli; Carlos López-Otín; Vicente Andrés
Journal:  EMBO Mol Med       Date:  2019-04       Impact factor: 12.137

6.  Vascular smooth muscle cell-specific progerin expression in a mouse model of Hutchinson-Gilford progeria syndrome promotes arterial stiffness: Therapeutic effect of dietary nitrite.

Authors:  Lara Del Campo; Amanda Sánchez-López; Mercedes Salaices; Ryan A von Kleeck; Elba Expósito; Cristina González-Gómez; Lorena Cussó; Gabriela Guzmán-Martínez; Jesús Ruiz-Cabello; Manuel Desco; Richard K Assoian; Ana M Briones; Vicente Andrés
Journal:  Aging Cell       Date:  2019-03-18       Impact factor: 9.304

7.  Vascular smooth muscle cell loss underpins the accelerated atherosclerosis in Hutchinson-Gilford progeria syndrome.

Authors:  Magda R Hamczyk; Vicente Andrés
Journal:  Nucleus       Date:  2019-12       Impact factor: 4.197

Review 8.  Molecular and Cellular Mechanisms Driving Cardiovascular Disease in Hutchinson-Gilford Progeria Syndrome: Lessons Learned from Animal Models.

Authors:  Ignacio Benedicto; Beatriz Dorado; Vicente Andrés
Journal:  Cells       Date:  2021-05-11       Impact factor: 6.600

9.  Towards delineating the chain of events that cause premature senescence in the accelerated aging syndrome Hutchinson-Gilford progeria (HGPS).

Authors:  Oliver Dreesen
Journal:  Biochem Soc Trans       Date:  2020-06-30       Impact factor: 5.407

Review 10.  Biomaterials and engineered microenvironments to control YAP/TAZ-dependent cell behaviour.

Authors:  Giovanna Brusatin; Tito Panciera; Alessandro Gandin; Anna Citron; Stefano Piccolo
Journal:  Nat Mater       Date:  2018-10-29       Impact factor: 43.841

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