A study in humans demonstrated that the miR-198 is upregulated four days post-burn in deep partial thickness burn skin compared to normal skin [Siu et al. DOI:10.1111/wrr.13100]. A study in mice demonstrated that elevated expression of the miR-198 in chronic wounds impairs keratinocyte migration and re-epithelialization [Badanina et al. DOI:10.3390/ijms262010060]. Research in human denatured dermis and heat-damaged fibroblasts further confirmed its dysregulation in thermal-induced skin injury, associating it with impaired wound healing processes [Wang & Zhou DOI:10.1007/s00438-024-02183-w].