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. 2024 Feb 20;11:rbae016. doi: 10.1093/rb/rbae016

Table 2.

Effects of mechanotransduction-targeted drugs in cell treatment

Agent/material Action mechanism Cells Outcomes Mechanical cues Ref.
Gsmtx4 Block CaN/NFAT1 signaling axis Rat primary chondrocytes Protect chondrocytes from apoptosis and anabolic/catabolic imbalance under mechanical strain Inhibited the deleterious effects of mechanical strain [209]
Andrographolide Activating the MAPK/Nrf2/HO-1 signaling pathway Nucleus pulposus cells Inhibits static mechanical pressure-induced apoptosis and improves cell viability Suppress static mechanical pressure-induced ROS accumulation in the NPCs [210]
γ-Fe2O3 SPIONPs The opening of the Piezol mechanosensor Neural stem cells Regulates the directional differentiation of NSCs and neuron regeneration Increase the elastic modulus of the NSCs [211]
Y-27632 Inhibit RhoA/ROCK pathway Unknown Reduce internal resistance Stiffness-induced cell activation [212]
Morin Inhibit Hippo/YAP and TGF-β1/Smad pathways Hepatic stellate cells (HSCs) Show antifibrotic effect Stiffness-induced HSC activation [213]
Xanthohumol Mediate the GAS5/miR-27a signaling pathway Chondrocytes Protected chondrocytes and increased viability Protective effects against mechanical stimulation-induced ECM degradation [214]
Metuzumab Decrease β1 integrin/FAK/Akt activation via CD147 blockade
  • Hepatocellular

  • carcinoma (HCC)

Inhibit tumor growth and metastatic potentials Stiffness, shear stress or IFP-induced proliferation and metastasis of HCC cells [215]