[HTML][HTML] sGC agonist BAY1021189 promotes thoracic aortic dissection formation by accelerating vascular smooth muscle cell phenotype switch

H Jiang, Y Jiang, Y Qu, J Lv, H Zeng - European Journal of Pharmacology, 2023 - Elsevier
Thoracic aortic dissection (TAD) is common but lethal cardiovascular disease with high
mortality. This study aimed to expound whether and how sGC-PRKG1 signaling pathway …

CDKN2B-AS1 aggravates the pathogenesis of human thoracic aortic dissection by sponge to miR-320d

X Zhao, S Cheng, S Li, J Li, X Bai… - Journal of Cardiovascular …, 2020 - journals.lww.com
In the present study, the role and molecular mechanism of long noncoding RNA CDKN2B-
AS1 in human thoracic aortic dissection (TAD), a highly lethal cardiovascular disease, was …

LINC01278 sponges miR‐500b‐5p to regulate the expression of ACTG2 to control phenotypic switching in human vascular smooth muscle cells during aortic …

W Wang, Q Liu, Y Wang, H Piao, Z Zhu… - Journal of the …, 2021 - Am Heart Assoc
Background Phenotypic switching in vascular smooth muscle cells (VSMCs) is involved in
the pathogenesis of aortic dissection (AD). This study aims to explore the potential …

Inhibition of sphingosine-1-phosphate receptor 2 prevents thoracic aortic dissection and rupture

G Pan, M Liao, Y Dai, Y Li, X Yan, W Mai… - Frontiers in …, 2021 - frontiersin.org
Background: Numerous pieces of evidence have indicated that thoracic aortic dissection
(TAD) is an inflammatory disease. Sphingosine-1-phosphate receptor 2 (S1PR2) signaling …

[HTML][HTML] HSP90 inhibitor 17-DMAG effectively alleviated the progress of thoracic aortic dissection by suppressing smooth muscle cell phenotypic switch

Z Zhao, Y Wang, S Li, S Liu, Y Liu, Y Yu… - American Journal of …, 2019 - ncbi.nlm.nih.gov
Thoracic aortic dissection (TAD) is a highly lethal vascular disease characterized by medial
degeneration. Heat shock protein 90 (HSP90) had been proved as a potential target for a …

Anxa1 in smooth muscle cells protects against acute aortic dissection

C Zhou, Z Lin, H Cao, Y Chen, J Li… - Cardiovascular …, 2022 - academic.oup.com
Aims Acute aortic dissection (AAD) is a life-threatening disease with high morbidity and
mortality. Previous studies have showed that vascular smooth muscle cell (VSMC) …

Activation of AMP-activated protein kinase ablated the formation of aortic dissection by suppressing vascular inflammation and phenotypic switching of vascular …

L Lei, Y Zhou, T Wang, Z Zheng, L Chen… - International …, 2022 - Elsevier
Background Aortic dissection (AD) is a fatal vascular disease in absence of effective
pharmaceutical therapy. Adenosine monophosphate-activated protein kinase α (AMPKα) …

[HTML][HTML] TGF-β1 induces human aortic vascular smooth muscle cell phenotype switch through PI3K/AKT/ID2 signaling

SB Zhu, J Zhu, ZZ Zhou, EP Xi, RP Wang… - American journal of …, 2015 - ncbi.nlm.nih.gov
The vascular smooth muscle cell (VSMC) phenotypic switch is considered to be the key
pathophysiological change in various cardiovascular diseases, such as aortic dissection …

The activator protein-1 complex governs a vascular degenerative transcriptional programme in smooth muscle cells to trigger aortic dissection and rupture

Y Luo, J Luo, P An, Y Zhao, W Zhao… - European Heart …, 2024 - academic.oup.com
Abstract Background and Aims Stanford type A aortic dissection (AD) is a degenerative
aortic remodelling disease marked by an exceedingly high mortality without effective …

Progression of thoracic aortic dissection is aggravated by the hsa_circ_0007386/miR-1271-5P/IGF1R/AKT axis via induction of arterial smooth muscle cell apoptosis

X Xie, X Hong, S Hong, Y Huang, G Chen, Y Chen… - Biomedicines, 2023 - mdpi.com
Background: The molecular mechanisms associated with thoracic aortic dissection (TAD)
remain poorly understood. A comprehensive high-throughput sequencing-based analysis of …