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Small GTP-Binding Protein GDP Dissociation Stimulator Prevents Thoracic Aortic Aneurysm Formation and Rupture by Phenotypic Preservation of Aortic Smooth Muscle Cells
Author(s) -
Masamichi Nogi,
Kimio Satoh,
Shinichiro Sunamura,
Nobuhiro Kikuchi,
Taijyu Satoh,
Ryo Kurosawa,
Junichi Omura,
Md. Elias-Al-Mamun,
Mohammad Abdul Hai Siddique,
Kazuhiko Numano,
Shun Kudo,
Satoshi Miyata,
Masatoshi Akiyama,
Kiichiro Kumagai,
Shunsuke Kawamoto,
Yoshikatsu Saiki,
Hiroaki Shimokawa
Publication year - 2018
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/circulationaha.118.035648
Subject(s) - medicine , angiotensin ii , apolipoprotein e , ascending aorta , aortic aneurysm , aorta , thoracic aortic aneurysm , aortic dissection , aortic rupture , thoracic aorta , aneurysm , abdominal aortic aneurysm , cardiology , surgery , receptor , disease
Thoracic aortic aneurysm (TAA) and dissection are fatal diseases that cause aortic rupture and sudden death. The small GTP-binding protein GDP dissociation stimulator (SmgGDS) is a crucial mediator of the pleiotropic effects of statins. Previous studies revealed that reduced force generation in aortic smooth muscle cells (AoSMCs) causes TAA and thoracic aortic dissection.

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