Department of Urology, The First Hospital of Jilin University, Changchun, Jilin Province 130021, China.
Institute of Virology and AIDS Research, The First Hospital of Jilin University, Changchun, Jilin Province 130021, China.
Int J Biol Sci. 2019 Jan 24;15(3):688-700. doi: 10.7150/ijbs.30847. eCollection 2019.
Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) is an effective chemotherapeutic agent that specifically impairs cancer cells while sparing normal cells; however, some cancer cells develop resistance to TRAIL. Here, we identified Andrographolide, a diterpenoid lactone derived from a traditional herbal medicine , as an ideal sensitizer for TRAIL to overcome bladder cancer. Our results showed that combination treatment of Andro and TRAIL retarded growth, attenuated proliferation, decreased colony formation, inhibited migration and promoted caspases-mediated apoptosis in T24 cells. Additionally, the sensitization by Andro is achieved through up-regulation of death receptors (DR4 and DR5) of TRAIL in a -dependent manner. Crucially, Andro is also capable of inactivating NF-κB signaling pathway via transcriptional down-regulation p65/RelA, which is further contributed to enhancement of TRAIL-mediated cytotoxicity. These results indicated that non-toxic doses of Andrographolide sensitized bladder cancer cells to TRAIL-mediated apoptosis, suggesting it as an effective therapeutic agent for TRAIL resistant human bladder cancers.
肿瘤坏死因子相关凋亡诱导配体(TRAIL)是一种有效的化疗药物,它特异性地损伤癌细胞而不损伤正常细胞;然而,一些癌细胞对 TRAIL 产生了耐药性。在这里,我们鉴定出穿心莲内酯是一种来源于传统草药的二萜内酯,是克服膀胱癌的理想 TRAIL 增敏剂。我们的结果表明,穿心莲内酯与 TRAIL 的联合治疗可延缓 T24 细胞的生长,减弱增殖,减少集落形成,抑制迁移并促进半胱天冬酶介导的细胞凋亡。此外,穿心莲内酯的增敏作用是通过 TRAIL 的死亡受体(DR4 和 DR5)的上调实现的,这种上调依赖于 NF-κB 信号通路。至关重要的是,穿心莲内酯还能够通过转录下调 p65/RelA 使 NF-κB 信号通路失活,这进一步有助于增强 TRAIL 介导的细胞毒性。这些结果表明,非毒性剂量的穿心莲内酯使膀胱癌细胞对 TRAIL 介导的细胞凋亡敏感,表明它是治疗 TRAIL 耐药性人类膀胱癌的有效治疗剂。