DAB2IP: unifying cardiovascular pathogenesis and cardiovascular brain crosstalk
Yufan Zhou, Peiwen Yang, Hanxun He, Hao Liu, Ping Ye, Jiahong Xia

TL;DR
The DAB2IP gene plays a key role in linking cardiovascular diseases and brain disorders through multiple biological pathways.
Contribution
This paper highlights DAB2IP as a unifying factor in cardiovascular and neurological pathogenesis and crosstalk.
Findings
DAB2IP regulates inflammation, apoptosis, and plaque angiogenesis in atherosclerosis via multiple signaling pathways.
DAB2IP is genetically linked to coronary artery disease, aortic aneurysm, and aortic dissection.
DAB2IP influences brain processes like neuron migration and blood-brain barrier integrity in Alzheimer's disease models.
Abstract
Cardiovascular diseases and brain disorders collectively represent a major global health burden. Not only do they frequently occur as comorbidities, but their pathological mechanisms are also intricately linked through a complex network of cardiovascular-brain crosstalk. Cardiovascular diseases (CVDs) and neurological disorders together impose high global health burdens. The DAB2IP gene, initially characterized as a tumor suppressor, serves as a multifunctional regulator and performs roles in both the cardiovascular and neurological systems. In atherosclerosis (AS), DAB2IP suppresses the inflammation and apoptosis of endothelial cells (ECs) through the TNF signaling pathways, inhibits phenotypic switching of vascular smooth muscle cells (VSMCs) via the JAK-STAT and PI3K-Akt axes, and attenuates plaque angiogenesis via VEGF-related pathways. It is genetically associated with coronary…
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Taxonomy
TopicsBarrier Structure and Function Studies · Nuclear Receptors and Signaling · Cholesterol and Lipid Metabolism
