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Cited by 207

The DOI matches its Crossref record; 9 of the 9 references it cites were found in a registry or an index.

Endothelial microRNAs regulating the NF‐κB pathway and cell adhesion molecules during inflammation

Zhong, Liang, Simard, Martin J., Huot, Jacques·2018·The FASEB Journal

Abstract

The surface of endothelial cells is covered with cell adhesion molecules, including E‐selectin, intercellula adhesion molecule 1 (ICAM‐1), and vascular cell adhesion molecule 1 (VCAM‐ 1), that mediate the adhesion an extravasation of leukocytes and play pivotal roles in inflammatory response. microRNAs (miRNAs) regulate th expression of these important cell adhesion molecules through two distinct major mechanisms, namely via mod ulating the proinflammatory NF‐κB pathway, which controls their transcription, and via directly targeting them The present review highlights the role of various miRNAs in controlling the expression of E‐selectin, ICAM‐1, an VCAM‐1: a type of regulation that can be harnessed for therapeutic prevention of inflammation‐associated disease such as atherosclerosis and sepsis. The roles of secreted miRNAs as paracrine regulators, and cell adhesio molecule‐based miRNA delivery are also addressed.—Zhong, L., Simard, M. J., Huot, J. Endothelial microRNA regulating the NF‐κB pathway and cell adhesion molecules during inflammation. FASEB J . 32, 4070‐4084 (2018) www.fasebj.org

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Metadata

Authors
Zhong, L., Simard, M. J., & Huot, J.
Venue
The FASEB Journal
Publisher
Wiley
Published
2018-03-22
Volume
32
Issue
8
Pages
4070-4084
ISSN
  • 0892-6638 (ISSN-L)
  • 1530-6860
OpenAlex
W2792128273
Cited by
207
References
9
FWCI
4.94
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Endothelial microRNAs regulating the NF‐κB pathway and cell adhesion molecules during inflammation. https://app.cochat.ai/papers/10.1096/fj.201701536r
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Zhong, L., Simard, M. J., & Huot, J. (2018). Endothelial microRNAs regulating the NF‐κB pathway and cell adhesion molecules during inflammation. The FASEB Journal. https://doi.org/10.1096/fj.201701536r

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