Sato K, Aytac U, Yamochi T, Yamochi T, Ohnuma K, McKee K S, Morimoto C, Dang N H
Department of Lymphoma/Myeloma, MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, TX 77030, USA.
Br J Cancer. 2003 Oct 6;89(7):1366-74. doi: 10.1038/sj.bjc.6601253.
CD26/dipeptidyl peptidase IV (DPPIV) is a cell surface-bound ectopeptidase with important roles in T-cell activation and tumour biology. We now report that CD26/DPPIV enhances sensitivity to apoptosis induced by the antineoplastic agents doxorubicin and etoposide. In particular, CD26/DPPIV presence is associated with increased susceptibility to the mitochondrial pathway of apoptosis, documented by enhanced cleavage of poly (ADP ribose) polymerase (PARP), caspase-3 and caspase-9, Bcl-xl, and Apaf-1, as well as increased expression of death receptor 5 (DR5). We also show that the caspase-9-specific inhibitor z-LEHD-fmk inhibits drug-mediated apoptosis, leading to decreased PARP and caspase-3 cleavage, and reduced DR5 expression. Importantly, through detailed studies that demonstrate the association between topoisomerase II alpha expression and DPPIV activity, our data provide further evidence of the key role played by CD26 in biological processes.
CD26/二肽基肽酶IV(DPPIV)是一种细胞表面结合的外肽酶,在T细胞活化和肿瘤生物学中发挥重要作用。我们现在报告,CD26/DPPIV增强了对抗肿瘤药物阿霉素和依托泊苷诱导的细胞凋亡的敏感性。特别是,CD26/DPPIV的存在与对凋亡线粒体途径的易感性增加有关,这通过聚(ADP核糖)聚合酶(PARP)、半胱天冬酶-3和半胱天冬酶-9、Bcl-xl和凋亡蛋白酶激活因子-1(Apaf-1)的切割增强以及死亡受体5(DR5)的表达增加得以证明。我们还表明,半胱天冬酶-9特异性抑制剂z-LEHD-fmk抑制药物介导的细胞凋亡,导致PARP和半胱天冬酶-3切割减少以及DR5表达降低。重要的是,通过详细研究证明拓扑异构酶IIα表达与DPPIV活性之间的关联,我们的数据进一步证明了CD26在生物学过程中所起的关键作用。