Kaliberov S, Stackhouse M A, Kaliberova L, Zhou T, Buchsbaum D J
Department of Radiation Oncology, University of Alabama at Birmingham, 35294, USA.
Gene Ther. 2004 Apr;11(8):658-67. doi: 10.1038/sj.gt.3302215.
Specific activation of apoptosis in tumor cells offers a promising approach for cancer therapy. Induction of apoptosis leads to activation of specific proteases. Two major pathways for caspase activation in mammalian cells have been described. One apoptotic pathway involves members of the tumor necrosis factor family of cytokine receptors (eg death receptor 5 (DR5)). The other pathway is controlled by the Bcl-2 family of proteins. The purpose of this study was to investigate whether increased apoptosis occurs in human glioma cells following infection with a recombinant adenoviral vector encoding the human Bax gene under the control of human vascular endothelial growth factor (VEGF) promoter element (AdVEGFBax) in combination with an anti-human DR5 monoclonal antibody (TRA-8). Specific overexpression of exogenous Bax protein induced apoptosis and cell death in glioma cell lines, through activation of both caspase-8 and -9, leading to activation of downstream caspase-3. The relative sensitivity to AdVEGFBax for the glioma cell lines was U251MG>U373MG>U87MG>D54MG. The recently characterized TRA-8 monoclonal antibody induces apoptosis of most TRAIL-sensitive tumor cells by specific binding to DR5 receptors on the cellular membrane. TRA-8 induced rapid apoptosis and cell death in glioma cells, but did not demonstrate detectable cytotoxicity of primary normal human astrocytes. The efficiency of TRA-8-induced apoptosis was variable in different glioma cell lines. The relative sensitivity to TRA-8 was U373MG>U87MG>U251MG>D54MG. The combination of TRA-8 treatment and overexpression of Bax overcame TRA-8 resistance of glioma cells in vitro. Cell viability of U251MG cells was 71.1% for TRA-8 (100 ng/ml) alone, 75.9% for AdVEGFBax (5 MOI) alone and 41.1% for their combination as measured by MTS assay. Similar enhanced apoptosis results were obtained for the other glioma cell lines. In vivo studies demonstrated that the combined treatment significantly (P<0.05) suppressed the growth of U251MG xenografts and produced 60% complete tumor regressions without recurrence. These data suggest that the combination of TRA-8 treatment with specific overexpression of Bax using AdVEGFBax may be an effective approach for the treatment of human malignant gliomas.
肿瘤细胞凋亡的特异性激活为癌症治疗提供了一种很有前景的方法。凋亡的诱导会导致特定蛋白酶的激活。哺乳动物细胞中半胱天冬酶激活的两条主要途径已被描述。一条凋亡途径涉及细胞因子受体肿瘤坏死因子家族的成员(如死亡受体5(DR5))。另一条途径由Bcl-2蛋白家族控制。本研究的目的是调查在人血管内皮生长因子(VEGF)启动子元件(AdVEGFBax)控制下编码人Bax基因的重组腺病毒载体与抗人DR5单克隆抗体(TRA-8)联合感染后人胶质瘤细胞中是否会发生凋亡增加。外源性Bax蛋白的特异性过表达通过激活半胱天冬酶-8和-9诱导胶质瘤细胞系中的凋亡和细胞死亡,导致下游半胱天冬酶-3的激活。胶质瘤细胞系对AdVEGFBax的相对敏感性为U251MG>U373MG>U87MG>D54MG。最近鉴定的TRA-8单克隆抗体通过与细胞膜上的DR5受体特异性结合诱导大多数对肿瘤坏死因子相关凋亡诱导配体(TRAIL)敏感的肿瘤细胞凋亡。TRA-8在胶质瘤细胞中诱导快速凋亡和细胞死亡,但对原代正常人星形胶质细胞未显示出可检测到的细胞毒性。TRA-8诱导凋亡的效率在不同的胶质瘤细胞系中有所不同。对TRA-8的相对敏感性为U373MG>U87MG>U251MG>D54MG。TRA-8处理与Bax过表达的联合克服了胶质瘤细胞在体外对TRA-8的抗性。通过MTS测定法,单独使用TRA-8(100 ng/ml)时U251MG细胞的活力为71.1%,单独使用AdVEGFBax(5 MOI)时为75.9%,两者联合使用时为41.1%。其他胶质瘤细胞系也获得了类似的增强凋亡结果。体内研究表明,联合治疗显著(P<0.05)抑制了U251MG异种移植瘤的生长,并产生了60%的完全肿瘤消退且无复发。这些数据表明,TRA-8处理与使用AdVEGFBax特异性过表达Bax的联合可能是治疗人类恶性胶质瘤的有效方法。