瘢痕疙瘩
化学
信号转导
癌症研究
细胞生物学
信号蛋白
医学
细胞信号
地址1
胶原受体
机械转化
伤口愈合
作者
Jingping Wang,Songyun Zhao,Liqun Li,Yucang He
摘要
This letter critically evaluates the recent study by Hu et al. on collagen I–discoidin domain receptor 1 (DDR1) signalling in keloid inflammation, highlighting its role in activating NF-κB and STAT3 pathways. We discuss the potential of dual-target therapy involving DDR1 and adenosine diphosphate ribosylation factor 6 (ARF6) inhibition and identify areas for further exploration, including the involvement of co-receptors, intermediate signalling pathways and collagen remodelling. These insights may guide future therapeutic strategies for keloid treatment.
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