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新型 Akt 抑制剂 API-1 诱导 c-FLIP 降解,并与 TRAIL 协同作用增强凋亡,而不依赖于 Akt 抑制。

The novel Akt inhibitor API-1 induces c-FLIP degradation and synergizes with TRAIL to augment apoptosis independent of Akt inhibition.

机构信息

Department of Hematology and Medical Oncology, Winship Cancer Institute, Emory University School of Medicine, Atlanta, Georgia 30322, USA.

出版信息

Cancer Prev Res (Phila). 2012 Apr;5(4):612-20. doi: 10.1158/1940-6207.CAPR-11-0548. Epub 2012 Feb 16.

DOI:10.1158/1940-6207.CAPR-11-0548
PMID:22345097
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3324640/
Abstract

API-1 (pyrido[2,3-d]pyrimidines) is a novel small-molecule inhibitor of Akt, which acts by binding to Akt and preventing its membrane translocation and has promising preclinical antitumor activity. In this study, we reveal a novel function of API-1 in regulation of cellular FLICE-inhibitory protein (c-FLIP) levels and TRAIL-induced apoptosis, independent of Akt inhibition. API-1 effectively induced apoptosis in tested cancer cell lines including activation of caspase-8 and caspase-9. It reduced the levels of c-FLIP without increasing the expression of death receptor 4 (DR4) or DR5. Accordingly, it synergized with TRAIL to induce apoptosis. Enforced expression of ectopic c-FLIP did not attenuate API-1-induced apoptosis but inhibited its ability to enhance TRAIL-induced apoptosis. These data indicate that downregulation of c-FLIP mediates enhancement of TRAIL-induced apoptosis by API-1 but is not sufficient for API-1-induced apoptosis. API-1-induced reduction of c-FLIP could be blocked by the proteasome inhibitor MG132. Moreover, API-1 increased c-FLIP ubiquitination and decreased c-FLIP stability. These data together suggest that API-1 downregulates c-FLIP by facilitating its ubiquitination and proteasome-mediated degradation. Because other Akt inhibitors including API-2 and MK2206 had minimal effects on reducing c-FLIP and enhancement of TRAIL-induced apoptosis, it is likely that API-1 reduces c-FLIP and enhances TRAIL-induced apoptosis independent of its Akt-inhibitory activity.

摘要

API-1(吡啶并[2,3-d]嘧啶)是一种新型 Akt 小分子抑制剂,通过与 Akt 结合并阻止其膜易位,具有很有前景的临床前抗肿瘤活性。在这项研究中,我们揭示了 API-1 在调节细胞 FLICE 抑制蛋白(c-FLIP)水平和 TRAIL 诱导的细胞凋亡方面的新功能,这一功能不依赖于 Akt 抑制。API-1 可有效诱导包括半胱天冬酶-8 和半胱天冬酶-9 激活在内的多种测试癌细胞系发生凋亡。它降低 c-FLIP 水平,而不增加死亡受体 4(DR4)或 DR5 的表达。因此,它与 TRAIL 协同诱导细胞凋亡。过表达异位 c-FLIP 不仅不能减弱 API-1 诱导的细胞凋亡,反而抑制了它增强 TRAIL 诱导的细胞凋亡的能力。这些数据表明,下调 c-FLIP 介导了 API-1 增强 TRAIL 诱导的细胞凋亡,但不是 API-1 诱导细胞凋亡所必需的。API-1 诱导的 c-FLIP 减少可被蛋白酶体抑制剂 MG132 阻断。此外,API-1 增加了 c-FLIP 的泛素化并降低了 c-FLIP 的稳定性。这些数据共同表明,API-1 通过促进 c-FLIP 的泛素化和蛋白酶体介导的降解来下调 c-FLIP。由于其他 Akt 抑制剂,包括 API-2 和 MK2206,对降低 c-FLIP 和增强 TRAIL 诱导的细胞凋亡的作用很小,因此 API-1 降低 c-FLIP 和增强 TRAIL 诱导的细胞凋亡可能独立于其 Akt 抑制活性。

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Lung-cancer chemoprevention by induction of synthetic lethality in mutant KRAS premalignant cells in vitro and in vivo.体外和体内诱导突变 KRAS 前病变细胞合成致死性预防肺癌。
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蛋白酶体去泛素化酶抑制剂 b-AP15 通过稳定 DR5 增强 DR5 激活诱导的细胞凋亡。
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hnRNPK inhibits GSK3β Ser9 phosphorylation, thereby stabilizing c-FLIP and contributes to TRAIL resistance in H1299 lung adenocarcinoma cells.异质性核糖核蛋白K(hnRNPK)抑制糖原合成酶激酶3β(GSK3β)的丝氨酸9磷酸化,从而稳定c-FLIP,并导致H1299肺腺癌细胞对肿瘤坏死因子相关凋亡诱导配体(TRAIL)产生抗性。
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