Title : Tunicamycin potentiates cisplatin anticancer efficacy through the DPAGT1/Akt/ABCG2 pathway in mouse Xenograft models of human hepatocellular carcinoma.

Pub. Date : 2013 Dec

PMID : 24130050






4 Functional Relationships(s)
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1 Tunicamycin potentiates cisplatin anticancer efficacy through the DPAGT1/Akt/ABCG2 pathway in mouse Xenograft models of human hepatocellular carcinoma. Tunicamycin ATP binding cassette subfamily G member 2 (Junior blood group) Mus musculus
2 The N-linked glycosylation (NLG) inhibitor tunicamycin dramatically reduced ABCG2 expression, altered its subcellular localization, and reversed its drug efflux effect in multiple hepatocellular carcinoma cell lines. Tunicamycin ATP binding cassette subfamily G member 2 (Junior blood group) Mus musculus
3 Tunicamycin combined with cisplatin (CDDP) inhibited proliferating cell nuclear antigen (PCNA) expression and increased the cleavage of PARP; this effect was partially rescued by the overexpression of ABCG2 or Akt-myr. Tunicamycin ATP binding cassette subfamily G member 2 (Junior blood group) Mus musculus
4 In summary, our results suggest that tunicamycin may reverse the drug resistance and improve the efficacy of combination treatments for hepatocellular carcinomas by targeting the DPAGT1/Akt/ABCG2 pathway. Tunicamycin ATP binding cassette subfamily G member 2 (Junior blood group) Mus musculus