[No authors listed]
An increasing number of studies have demonstrated that tumor necrosis factorâstimulated geneâ6 (TSGâ6) has a key role in the progression of fibrosis; however, the exact effects of TSGâ6 in keloid fibroblasts (KFs) remain unknown. The aim of the current study was to investigate the role of TSGâ6 in the pathogenesis of keloids. Primary fibroblasts from 10Â patients with keloid were cultured and transfected with pLVXâPuro or pLVXâPuroâTSGâ6. Alterations of TSGâ6 expression were then determined by reverse transcriptionâpolymerase chain reaction (RTâPCR) and regulation was observed in KFs transfected with pLVXâPuroâTSGâ6. Compared with the control group, transfection with pLVXâPuroâTSGâ6 induced growth suppression, cell apoptosis and G2/M arrest in KFs. In addition, the mitochondrial apoptosis pathway was activated in KFs transfected with pLVXâPuroâTSGâ6. These findings indicate that TSGâ6 is a novel regulator of keloid fibrogenesis, and thus could be used/targeted TSGâ6 as a promising treatment for keloid.
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