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BAG-1 is up-regulated in colorectal tumour progression and promotes colorectal tumour cell survival through increased NF-κB activity

Research output: Contribution to journalArticle

Original languageEnglish
Pages (from-to)849 - 857
Number of pages9
Issue number4
Early online date19 Jan 2008
DateE-pub ahead of print - 19 Jan 2008
DatePublished (current) - Apr 2008


Although expression of the anti-apoptotic protein Bcl-2-associated athanogene-1 (BAG-1) has been reported as up-regulated in a number of malignancies, we show for the first time that BAG-1 is over-expressed in medium/large-sized colorectal adenomas and carcinomas compared with normal epithelium. To investigate whether expression of BAG-1 is important for colorectal tumour cell survival, microarray analysis was carried out on the HCT116 colorectal carcinoma cell line following transfection with BAG-1 small interfering RNA (siRNA). Analysis identified altered expression of a subset of potential nuclear factor-{kappa}B (NF-{kappa}B)-regulated genes. Furthermore, knock down of BAG-1 was shown to inhibit NF-{kappa}B transcriptional activity. Inhibition of NF-{kappa}B activity using BAG-1 siRNA or the NF-{kappa}B inhibitor BAY-117082 suppressed HCT116 cell yield and induced apoptosis; combined treatment had no additive effect, suggesting that the decrease in cell yield associated with knock down of BAG-1 expression is mediated via inhibition of NF-{kappa}B. Of clinical relevance, BAG-1 siRNA sensitized colorectal carcinoma cells to apoptosis induced by potential therapeutic agent TRAIL as well as tumour necrosis factor-{alpha}, both inducers of NF-{kappa}B activity. In summary, knock down of BAG-1 leads to inhibition of NF-{kappa}B, identifying BAG-1 as a novel regulator of NF-{kappa}B. It is proposed that, by inhibiting NF-{kappa}B, suppression of BAG-1 could represent a novel strategy to impede colorectal cancer cell survival and as an adjuvant increase sensitivity to current therapeutic regimes.

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Publisher: Oxford University Press

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