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10.1038/s41598-017-14893-w

http://scihub22266oqcxt.onion/10.1038/s41598-017-14893-w
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C5678438!5678438!29118355
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suck abstract from ncbi


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pmid29118355      Sci+Rep 2017 ; 7 (ä): ä
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  • Decoy Wnt receptor (sLRP6E1E2)-expressing adenovirus induces anti-fibrotic effect via inhibition of Wnt and TGF-? signaling #MMPMID29118355
  • Lee WJ; Lee JS; Ahn HM; Na Y; Yang CE; Lee JH; Hong J; Yun CO
  • Sci Rep 2017[]; 7 (ä): ä PMID29118355show ga
  • Aberrant activation of the canonical Wingless type (Wnt) signaling pathway plays a key role in the development of hypertrophic scars and keloids, and this aberrant activation of Wnt pathway can be a potential target for the development of novel anti-fibrotic agents. In this study, we evaluated the anti-fibrotic potential of a soluble Wnt decoy receptor (sLRP6E1E2)-expressing non-replicating adenovirus (Ad; dE1-k35/sLRP6E1E2) on human dermal fibroblasts (HDFs), keloid fibroblasts (KFs), and keloid tissue explants. Higher Wnt3a and ?-catenin expression was observed in the keloid region compared to the adjacent normal tissues. The activity of ?-catenin and mRNA expression of type-I and -III collagen were significantly decreased following treatment with dE1-k35/sLRP6E1E2 in HDFs and KFs. The expression of LRP6, ?-catenin, phosphorylated glycogen synthase kinase 3 beta, Smad 2/3 complex, and TGF-?1 were decreased in Wnt3a- or TGF-?1-activated HDFs, following administration of dE1-k35/sLRP6E1E2. Moreover, dE1-k35/sLRP6E1E2 markedly inhibited nuclear translocation of both ?-catenin and Smad 2/3 complex. The expression levels of type-I and -III collagen, fibronectin, and elastin were also significantly reduced in keloid tissue explants after treatment with dE1-k35/sLRP6E1E2. These results indicate that Wnt decoy receptor-expressing Ad can degrade extracellular matrix in HDFs, KFs, and primary keloid tissue explants, and thus it may be beneficial for treatment of keloids.
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