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• W2152440529 startingPage "1273" @default.
• W2152440529 abstract "Glucose-regulated protein 78 (GRP78) is one of the most important responders to disease-related stress. We assessed the association of the promoter polymorphisms of GRP78 with risk of hepatocellular carcinoma (HCC) and GRP78 expression in a Chinese population. We examined 1007 patients undergoing diagnostic HCC and 810 unrelated healthy controls. Mechanisms by which the GRP78 promoter polymorphism modulates HCC risk and GRP78 levels were analyzed. The promoter haplotype and diplotype carrying rs391957 (-415bp) allele G and genotype GG was strongly associated with HCC risk. Luciferase reporter assays indicated that the promoter carrying rs391957 allele G (haplotype GCCd) showed increased activity in HepG2 cells and Hela cells. rs391957 was also shown to increase the affinity of the transcriptional activator Ets-2, the resistance to apoptosis, as well as cell instability in stressful microenvironment. Furthermore, compared with allele A, rs391957 allele G was associated with higher levels of GRP78 mRNA and protein in HCC tissues. These findings provided new insights into the pathogenesis of HCC and an unexpected effect of the interaction between rs391957 and Ets-2 on hepatocarcinogenesis, and especially supported the hypothesis that stress-related and evolutionarily conserved genetic variant(s) influencing transcriptional regulation could predict susceptibilities." @default.
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• W2152440529 date "2013-02-15" @default.
• W2152440529 modified "2023-10-05" @default.
• W2152440529 title "The rs391957 variant cis-regulating oncogene GRP78 expression contributes to the risk of hepatocellular carcinoma" @default.
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• W2152440529 doi "https://doi.org/10.1093/carcin/bgt061" @default.
• W2152440529 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/23416888" @default.
• W2152440529 hasPublicationYear "2013" @default.
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