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Publication : LIG4 mediates Wnt signalling-induced radioresistance.

First Author  Jun S Year  2016
Journal  Nat Commun Volume  7
Pages  10994 PubMed ID  27009971
Mgi Jnum  J:236835 Mgi Id  MGI:5807335
Doi  10.1038/ncomms10994 Citation  Jun S, et al. (2016) LIG4 mediates Wnt signalling-induced radioresistance. Nat Commun 7:10994
abstractText  Despite the implication of Wnt signalling in radioresistance, the underlying mechanisms are unknown. Here we find that high Wnt signalling is associated with radioresistance in colorectal cancer (CRC) cells and intestinal stem cells (ISCs). We find that LIG4, a DNA ligase in DNA double-strand break repair, is a direct target of beta-catenin. Wnt signalling enhances non-homologous end-joining repair in CRC, which is mediated by LIG4 transactivated by beta-catenin. During radiation-induced intestinal regeneration, LIG4 mainly expressed in the crypts is conditionally upregulated in ISCs, accompanied by Wnt/beta-catenin signalling activation. Importantly, among the DNA repair genes, LIG4 is highly upregulated in human CRC cells, in correlation with beta-catenin hyperactivation. Furthermore, blocking LIG4 sensitizes CRC cells to radiation. Our results reveal the molecular mechanism of Wnt signalling-induced radioresistance in CRC and ISCs, and further unveils the unexpected convergence between Wnt signalling and DNA repair pathways in tumorigenesis and tissue regeneration.
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