Hematology-Oncology Laboratory, Pediatrics Department, University of Padova, Padova, Italy.
PLoS One. 2011;6(10):e26097. doi: 10.1371/journal.pone.0026097. Epub 2011 Oct 10.
BCL2 associated Athano-Gene 1 (BAG1) is a multifunctional protein that has been described to be involved in different cell processes linked to cell survival. It has been reported as deregulated in diverse cancer types. Here, BAG1 protein was found highly expressed in children with acute myeloid leukemia at diagnosis, and in a cohort of leukemic cell lines. A silencing approach was used for determining BAG1's role in AML, finding that its down-regulation decreased expression of BCL2, BCL-XL, MCL1, and phospho-ERK1/2, all proteins able to sustain leukemia, without affecting the pro-apoptotic protein BAX. BAG1 down-regulation was also found to increase expression of BAG3, whose similar activity was able to compensate the loss of function of BAG1. BAG1/BAG3 co-silencing caused an enhanced cell predisposition to death in cell lines and also in primary AML cultures, affecting the same proteins. Cell death was CASPASE-3 dependent, was accompanied by PARP cleavage and documented by an increased release of pro-apoptotic molecules Smac/DIABLO and Cytochrome c. BAG1 was found to directly maintain BCL2 and to protect MCL1 from proteasomal degradation by controlling USP9X expression, which appeared to be its novel target. Finally, BAG1 was found able to affect leukemia cell fate by influencing the expression of anti-apoptotic proteins crucial for AML maintenance.
Bcl-2 相关的 Athanogene 1(BAG1)是一种多功能蛋白,已被描述参与与细胞存活相关的不同细胞过程。它在多种癌症类型中被报道失调。在这里,BAG1 蛋白在诊断时患有急性髓细胞白血病的儿童和一组白血病细胞系中表达水平较高。采用沉默方法确定 BAG1 在 AML 中的作用,发现其下调降低了 BCL2、BCL-XL、MCL1 和磷酸化 ERK1/2 的表达,所有这些蛋白都能够维持白血病,而不影响促凋亡蛋白 BAX。BAG1 的下调还发现增加了 BAG3 的表达,其相似的活性能够补偿 BAG1 的功能丧失。BAG1/BAG3 共沉默导致细胞系和原代 AML 培养物中细胞对死亡的易感性增加,影响相同的蛋白。细胞死亡依赖于 CASPASE-3,伴随着 PARP 切割,并通过增加促凋亡分子 Smac/DIABLO 和细胞色素 c 的释放来证明。发现 BAG1 通过控制 USP9X 的表达来直接维持 BCL2 并保护 MCL1 免受蛋白酶体降解,这似乎是其新的靶标。最后,发现 BAG1 通过影响对 AML 维持至关重要的抗凋亡蛋白的表达来影响白血病细胞的命运。