School of Biomedical Sciences, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong Special Administrative Region, China.
School of Biomedical Sciences, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong Special Administrative Region, China.
J Exp Clin Cancer Res. 2020 Nov 26;39(1):262. doi: 10.1186/s13046-020-01763-z.
Recent genomic analyses revealed that druggable molecule targets were only detectable in approximately 6% of patients with nasopharyngeal carcinoma (NPC). However, a dependency on dysregulated CDK4/6-cyclinD1 pathway signaling is an essential event in the pathogenesis of NPC. In this study, we aimed to evaluate the therapeutic efficacy of a specific CDK4/6 inhibitor, palbociclib, and its compatibility with other chemotherapeutic drugs for the treatment of NPC by using newly established xenograft models and cell lines derived from primary, recurrent, and metastatic NPC.
We evaluated the efficacies of palbociclib monotherapy and concurrent treatment with palbociclib and cisplatin or suberanilohydroxamic acid (SAHA) in NPC cell lines and xenograft models. RNA sequencing was then used to profile the drug response-related pathways. Palbociclib-resistant NPC cell lines were established to determine the potential use of cisplatin as a second-line treatment after the development of palbociclib resistance. We further examined the efficacy of palbociclib treatment against cisplatin-resistant NPC cells.
In NPC cells, palbociclib monotherapy was confirmed to induce cell cycle arrest in the G1 phase in vitro. Palbociclib monotherapy also had significant inhibitory effects in all six tested NPC tumor models in vivo, as indicated by substantial reductions in the total tumor volumes and in Ki-67 proliferation marker expression. In NPC cells, concurrent palbociclib treatment mitigated the cytotoxic effect of cisplatin in vitro. Notably, concurrent treatment with palbociclib and SAHA synergistically promoted NPC cell death both in vitro and in vivo. This combination also further inhibited tumor growth by inducing autophagy-associated cell death. NPC cell lines with induced palbociclib or cisplatin resistance remained sensitive to treatment with cisplatin or palbociclib, respectively.
Our study findings provide essential support for the use of palbociclib as an alternative therapy for NPC and increase awareness of the effective timing of palbociclib administration with other chemotherapeutic drugs. Our results provide a foundation for the design of first-in-human clinical trials of palbociclib regimens in patients with NPC.
最近的基因组分析显示,可用药分子靶点仅在大约 6%的鼻咽癌(NPC)患者中可检测到。然而,CDK4/6-cyclinD1 通路信号的失调依赖是 NPC 发病机制中的一个重要事件。在这项研究中,我们旨在通过使用新建立的异种移植模型和源自原发性、复发性和转移性 NPC 的细胞系,评估特定的 CDK4/6 抑制剂 palbociclib 的治疗效果及其与其他化疗药物联合治疗 NPC 的效果。
我们评估了 palbociclib 单药治疗以及 palbociclib 与顺铂或 suberanilohydroxamic acid (SAHA) 联合治疗 NPC 细胞系和异种移植模型的疗效。然后使用 RNA 测序来描绘药物反应相关途径。建立 palbociclib 耐药 NPC 细胞系,以确定在开发 palbociclib 耐药后顺铂作为二线治疗的潜在用途。我们进一步研究了 palbociclib 治疗对顺铂耐药 NPC 细胞的疗效。
在 NPC 细胞中,体外实验证实 palbociclib 单药治疗可诱导细胞周期停滞在 G1 期。Palbociclib 单药治疗在体内所有六种测试的 NPC 肿瘤模型中也具有显著的抑制作用,表现为总肿瘤体积和 Ki-67 增殖标志物表达的显著减少。在 NPC 细胞中,palbociclib 联合治疗减轻了顺铂的细胞毒性作用。值得注意的是,palbociclib 和 SAHA 联合治疗在体外和体内均协同促进 NPC 细胞死亡,通过诱导自噬相关细胞死亡进一步抑制肿瘤生长。诱导 palbociclib 或顺铂耐药的 NPC 细胞系对顺铂或 palbociclib 的治疗仍敏感。
我们的研究结果为 palbociclib 作为 NPC 的替代治疗提供了重要支持,并提高了对 palbociclib 与其他化疗药物联合治疗的有效时机的认识。我们的结果为设计 NPC 患者的 palbociclib 方案首次人体临床试验提供了基础。