Moores Cancer Center, Division of Hematology-Oncology, Department of Medicine, School of Medicine, University of California San Diego, La Jolla, California, United States of America.
PLoS One. 2013 Oct 11;8(10):e77495. doi: 10.1371/journal.pone.0077495. eCollection 2013.
TNF-Related Apoptosis Inducing Ligand (TRAIL) binds to and activates death receptors to stimulate caspase-8 and apoptosis with higher efficiency in cancer than normal cells but the development of apoptosis resistance has limited its clinical efficacy. We found that stable, but not transient knockdown of the ABL tyrosine kinase enhanced the apoptotic response to TRAIL. Re-expression of Abl, but not its nuclear import- or kinase-defective mutant, in the ABL-knockdown cells re-established apoptosis suppression. TRAIL is known to stimulate caspase-8 ubiquitination (Ub-C8), which can facilitate caspase-8 activation or degradation by the lysosomes. In the ABL-knockdown cells, we found a higher basal level of Ub-C8 that was not further increased by lysosomal inhibition. Re-expression of Abl in the ABL-knockdown cells reduced the basal Ub-C8, correlating with apoptosis suppression. We found that lysosomal inhibition by chloroquine (CQ) could also enhance TRAIL-induced apoptosis. However, this pro-apoptotic effect of CQ was lost in the ABL-knockdown cells but restored by Abl re-expression. Interestingly, kinase inhibition at the time of TRAIL stimulation was not sufficient to enhance apoptosis. Instead, persistent treatment for several days with imatinib, an ABL kinase inhibitor, was required to cause the enhanced and the CQ-insensitive apoptotic response to TRAIL. Together, these results show that persistent loss of nuclear ABL tyrosine kinase function can sensitize cells to TRAIL and suggest that long-term exposure to the FDA-approved ABL kinase inhibitors may potentiate apoptotic response to TRAIL-based cancer therapy.
肿瘤坏死因子相关凋亡诱导配体(TRAIL)与死亡受体结合并激活,从而在癌细胞中比正常细胞更有效地刺激半胱天冬酶-8 和细胞凋亡,但凋亡抵抗的发展限制了其临床疗效。我们发现,ABL 酪氨酸激酶的稳定但非瞬时敲低增强了对 TRAIL 的凋亡反应。在 ABL 敲低细胞中重新表达 Abl,但不是其核导入或激酶缺陷突变体,重新建立了凋亡抑制。已知 TRAIL 刺激半胱天冬酶-8 泛素化(Ub-C8),这可以促进半胱天冬酶-8 的激活或溶酶体降解。在 ABL 敲低细胞中,我们发现 Ub-C8 的基础水平较高,溶酶体抑制后不会进一步增加。在 ABL 敲低细胞中重新表达 Abl 可降低基础 Ub-C8,与凋亡抑制相关。我们发现氯喹(CQ)对溶酶体的抑制也可以增强 TRAIL 诱导的细胞凋亡。然而,CQ 的这种促凋亡作用在 ABL 敲低细胞中丧失,但通过 Abl 重新表达得以恢复。有趣的是,在 TRAIL 刺激时的激酶抑制不足以增强凋亡。相反,需要用 ABL 激酶抑制剂伊马替尼持续治疗数天,才能引起对 TRAIL 的增强和 CQ 不敏感的凋亡反应。总之,这些结果表明,持续丧失核 ABL 酪氨酸激酶功能可使细胞对 TRAIL 敏感,并表明长期暴露于美国食品和药物管理局批准的 ABL 激酶抑制剂可能增强基于 TRAIL 的癌症治疗的凋亡反应。