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