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The retinoblastoma protein (Rb) as an anti-apoptotic factor: expression of Rb is required for the anti-apoptotic function of BAG-1 protein in colorectal tumour cells

机译:视网膜母细胞瘤蛋白(Rb)作为抗凋亡因子:Rb的表达是BAG-1蛋白在结直肠肿瘤细胞中的抗凋亡功能所必需的

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摘要

Although the retinoblastoma-susceptibility gene RB1 is inactivated in a wide range of human tumours, in colorectal cancer, the retinoblastoma protein (Rb) function is often preserved and the RB locus even amplified. Importantly, we have previously shown that Rb interacts with the anti-apoptotic Bcl-2 associated athanogene 1 (BAG-1) protein, which is highly expressed in colorectal carcinogenesis. Here we show for the first time that Rb expression is critical for BAG-1 anti-apoptotic activity in colorectal tumour cells. We demonstrate that Rb expression not only increases the nuclear localisation of the anti-apoptotic BAG-1 protein, but that expression of Rb is required for inhibition of apoptosis by BAG-1 both in a γ-irradiated Saos-2 osteosarcoma cell line and colorectal adenoma and carcinoma cell lines. Further, consistent with the fact that nuclear BAG-1 has previously been shown to promote cell survival through increasing nuclear factor (NF)-κB activity, we demonstrate that the ability of BAG-1 to promote NF-κB activity is significantly inhibited by repression of Rb expression. Taken together, data presented suggest a novel function for Rb, promoting cell survival through regulating the function of BAG-1. As BAG-1 is highly expressed in the majority of colorectal tumours, targeting the Rb–BAG-1 complex to promote apoptosis has exciting potential for future therapeutic development.
机译:尽管视网膜母细胞瘤敏感性基因RB1在多种人类肿瘤中均失活,但在大肠癌中,视网膜母细胞瘤蛋白(Rb)的功能通常得以保留,并且RB基因座甚至被扩增。重要的是,我们以前已经证明Rb与抗凋亡Bcl-2相关的致癌基因1(BAG-1)蛋白相互作用,该蛋白在结直肠癌发生中高度表达。在这里,我们首次显示Rb表达对于结直肠肿瘤细胞中BAG-1抗凋亡活性至关重要。我们证明Rb表达不仅增加抗凋亡的BAG-1蛋白的核定位,而且Rb的表达是γ-射线照射的Saos-2骨肉瘤细胞系和结直肠中BAG-1抑制细胞凋亡所必需的腺瘤和癌细胞系。此外,与先前已显示核BAG-1可通过增加核因子(NF)-κB活性来促进细胞存活的事实相符,我们证明了BAG-1促进NF-κB活性的能力受到抑制的显着抑制Rb表达。两者合计,提供的数据表明Rb的新功能,通过调节BAG-1的功能促进细胞存活。由于BAG-1在大多数结直肠肿瘤中高表达,因此靶向Rb–BAG-1复合物以促进细胞凋亡具有令人兴奋的未来治疗发展潜力。

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