Fulda Simone, Meyer Eric, Debatin Klaus-Michael
University Children's Hospital, Prittwitzstr. 43, D-89075 Ulm, Germany.
Oncogene. 2002 Apr 4;21(15):2283-94. doi: 10.1038/sj.onc.1205258.
Primary or acquired resistance to current treatment protocols remains a major concern in clinical oncology and may be caused by defects in apoptosis programs. Since recent data suggest that TRAIL can bypass apoptosis resistance caused by Bcl-2, we further investigated the role of Bcl-2 in TRAIL-induced apoptosis. Here we report that overexpression of Bcl-2 conferred protection against TRAIL in neuroblastoma, glioblastoma or breast carcinoma cell lines. Bcl-2 overexpression reduced TRAIL-induced cleavage of caspase-8 and Bid indicating that caspase-8 was activated upstream and also downstream of mitochondria in a feedback amplification loop. Importantly, Bcl-2 blocked cleavage of caspases-9, -7 and -3 into active subunits and cleavage of the caspase substrates DFF45 or PARP. Also, Bcl-2 blocked cleavage of XIAP and overexpression of XIAP conferred resistance against TRAIL indicating that apoptosis was also amplified through a feedforward loop between caspases and XIAP. In contrast, in SKW lymphoblastoid cells, TRAIL-induced activation of caspase-8 directly translated into full activation of caspases, cleavage of XIAP, DFF45 or PARP and apoptosis independent of Bcl-2 overexpression, although Bcl-2 similarly inhibited loss of mitochondrial membrane potential and the release of cytochrome c, AIF and Smac from mitochondria in all cell types. By demonstrating a cell type dependent regulation of the TRAIL signaling pathway at different level, e.g. by Bcl-2 and by XIAP, these findings may have important clinical implication. Thus, strategies targeting the molecular basis of resistance towards TRAIL may be necessary in some tumors for cancer therapy with TRAIL.
对当前治疗方案的原发性或获得性耐药仍然是临床肿瘤学中的一个主要问题,可能由凋亡程序缺陷引起。由于最近的数据表明肿瘤坏死因子相关凋亡诱导配体(TRAIL)可以绕过由Bcl-2引起的凋亡抗性,我们进一步研究了Bcl-2在TRAIL诱导的凋亡中的作用。在此我们报告,在神经母细胞瘤、胶质母细胞瘤或乳腺癌细胞系中,Bcl-2的过表达赋予了对TRAIL的保护作用。Bcl-2过表达减少了TRAIL诱导的半胱天冬酶-8(caspase-8)和Bid的切割,表明caspase-8在反馈放大环中在线粒体的上游和下游均被激活。重要的是,Bcl-2阻止了半胱天冬酶-9、-7和-3切割成活性亚基以及半胱天冬酶底物DNA片段化因子45(DFF45)或聚(ADP-核糖)聚合酶(PARP)的切割。此外,Bcl-2阻止了X连锁凋亡抑制蛋白(XIAP)的切割,并且XIAP的过表达赋予了对TRAIL的抗性,表明凋亡也通过半胱天冬酶和XIAP之间的前馈环被放大。相反,在SKW淋巴母细胞系中,TRAIL诱导的caspase-8激活直接转化为半胱天冬酶的完全激活、XIAP、DFF45或PARP的切割以及凋亡,与Bcl-2过表达无关,尽管Bcl-2同样抑制了所有细胞类型中线粒体膜电位的丧失以及细胞色素c、凋亡诱导因子(AIF)和第二线粒体来源的促凋亡蛋白(Smac)从线粒体的释放。通过证明在不同水平(例如通过Bcl-2和XIAP)对TRAIL信号通路的细胞类型依赖性调节,这些发现可能具有重要的临床意义。因此,在某些肿瘤中,针对TRAIL抗性分子基础的策略对于使用TRAIL进行癌症治疗可能是必要的。