Transcriptional regulation of bcl-2 by nuclear factor kappa B and its significance in prostate cancer

This work presents direct evidence that the, bcl-2 gene is transcriptionall y, regulated by nuclear factor-kappaB (NF-kappaB) and directly links the TN F-alpha /NF-kappaB signaling pathway with Bcl-2 expression and its pro-surv ival response in human prostate carcinoma cells. DNase I footprinting, gel retardation and supershift analysis identified a NF-kappaB site in the bcl- 2 p2 promoter. In the context of a minimal promoter, this bcl-2 p2 site 1 i ncreased transcription 10-fold in the presence of the p50/p65, expression v ectors, comparable to the increment observed with the consensus NF-kappaB s ite, while for the full p2 promoter region transcriptional activity was inc reased sixfold by over-expression of NF-kappaB, an effect eliminated by mut ating the bcl-2 p2 site 1. The expression of Bcl-2 has been linked to the h ormone-resistant phenotype of advanced prostate cancer. Here we show that a n increase in the level of expression of Bcl-2 in the human prostate carcin oma cell line LNCaP observed in response to hormone withdrawal is further a ugmented by TNF-alpha treatment, and this effect is abated by inhibitors of NF-kappaB. Concomitantly, bcl-2 p2 promoter studies in LNCaP cells, show a 40-fold increase in promoter activity after stimulation with TNF-alpha in the absence of hormone.