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Updated: May 27, 2026

Synthesis of Monocyte-targeting Peptide Amphiphile Micelles for Imaging of Atherosclerosis
Published on: November 17, 2017
Cell adhesion molecules as pharmaceutical target in atherosclerosis
S Ling1, L Nheu, P A Komesaroff
1Department of Medicine, Monash University Central Clinical School, Alfred Centre, 99 Commercial Road, Prahran, Melbourne, Victoria 3181, Australia. shanhong.ling@monash.edu
Cell adhesion molecules (CAMs) are key in atherosclerosis development by promoting leukocyte recruitment. Targeting CAMs with new drugs offers promising therapeutic strategies for cardiovascular diseases.
Area of Science:
- Biochemistry
- Immunology
- Cardiovascular Medicine
Background:
- Cell adhesion molecules (CAMs) are transmembrane proteins crucial for cell-cell and cell-extracellular matrix interactions.
- Their increased expression and activation in vascular endothelium and leukocytes contribute to leukocyte recruitment in atherosclerosis pathogenesis.
- Conditions like inflammation, hypercholesterolemia, hypertension, and diabetes exacerbate CAMs' role in atherogenesis.
Purpose of the Study:
- To review recent advancements in understanding the pathophysiology of CAMs in atherogenesis.
- To survey pharmaceutical agents and chemicals targeting CAMs.
- To assess the potential for clinical development in preventing, monitoring, and treating atherosclerotic cardiovascular diseases.
Main Methods:
- Literature review of recent scientific publications.
- Analysis of studies on CAMs' role in atherosclerosis.
- Evaluation of pharmaceutical agents targeting CAMs' production and function.
Main Results:
- CAMs play a significant role in leukocyte recruitment, a critical step in atherosclerosis.
- Various pharmaceutical agents and chemicals have been developed to modulate CAMs.
- These agents show potential for clinical application in managing atherosclerotic cardiovascular diseases.
Conclusions:
- CAMs are pivotal in the inflammatory processes underlying atherosclerosis.
- Targeting CAMs represents a promising therapeutic avenue for cardiovascular diseases.
- Further clinical development of CAM-targeting agents could improve patient outcomes.
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