Hepatocyte Growth Factor DNA Aptamer for Prevention of Postoperative Peritoneal Adhesion via Enhancement of Fibrinolysis and Inhibition of Mesothelial Mesenchymal Transition.
Yizhou DaiNatsuko F InagakiRyosuke UekiShinsuke SandoKiyoshi HasegawaTaichi ItoPublished in: ACS applied bio materials (2024)
Postoperative peritoneal adhesion (PPA) is a prevalent complication of abdominal surgery, posing a significant hindrance to postsurgical recovery. Although several strategies have been developed to alleviate and prevent adhesions, their efficacy remains unsatisfactory. For the first time, we studied the therapeutic effect and mechanism of our recently developed thermally stable oligonucleotide-based mimetics of hepatocyte growth factor (HGF DNA aptamer) to prevent PPA. The HGF DNA aptamer effectively inhibited canonical TGF-β1 signaling transduction, partially suppressing mesothelial mesenchymal transition. Additionally, the aptamer, respectively, upregulated and downregulated the expression of tissue plasminogen activator and plasminogen activator inhibitor 1, thereby enhancing fibrinolytic activity. As a pleiotropic factor, the HGF DNA aptamer also enhanced the migratory and proliferative capacities of mesothelial cells. Finally, the aptamer demonstrated a higher level of effectiveness in preventing PPAs than the commercially available antiperitoneal adhesion barrier, Seprafilm. Due to its therapeutic benefits, excellent stability, biosafety, cost-effectiveness, and versatility, the HGF DNA aptamer demonstrates promise for preventing PPA in future clinical settings.
Keyphrases
- growth factor
- gold nanoparticles
- circulating tumor
- sensitive detection
- cell free
- magnetic nanoparticles
- single molecule
- label free
- stem cells
- nucleic acid
- randomized controlled trial
- bone marrow
- patients undergoing
- poor prognosis
- biofilm formation
- induced apoptosis
- systematic review
- circulating tumor cells
- signaling pathway
- oxidative stress
- high glucose
- deep learning
- cell death
- endothelial cells
- cell proliferation
- binding protein
- drug induced