Fukushima Hiroto, Abe Tetsuya, Sakamoto Kazuki, Tsujimoto Hiroaki, Mizuarai Shinji, Oie Shinji
Biomarker Research, Tsukuba Research Center, Taiho Pharmaceutical Co,, Ltd, 3 Okubo, Tsukuba, Ibaraki 300-2611, Japan.
BMC Cancer. 2014 Aug 4;14:562. doi: 10.1186/1471-2407-14-562.
We previously reported that 3'-ethynylcytidine (ECyd, TAS-106), an RNA polymerases inhibitor, enhances the anti-tumor efficacy of platinum in several tumor types in both in vitro and in vivo tumor models. However, the molecular mechanisms underlying the ECyd-induced enhancement remain elusive.
Cisplatin (CDDP)-resistant head and neck cancer KB cells were established by stepwise dose escalation with CDDP. The combination effect of ECyd and CDDP were assessed using isobologram analysis. The transcriptional and post-translational statuses of several molecules were detected using real-time PCR, immunoblot analysis and immunocytochemistry. Xenograft assays were used to confirm the mechanisms underlying the ECyd induced enhancement of CDDP anti-tumor efficacy in vivo.
ECyd sensitized KB to CDDP by inhibiting the drug transporter Vault complex (Vaults). First, we showed that Vaults were overexpressed in CDDP-resistant KB cells. The suppression of major vault protein (MVP) by RNA interference restored the sensitivity to CDDP. Next, we showed that ECyd significantly sensitized the resistant cells to CDDP, compared with the parental paired cell line. A molecular analysis revealed that ECyd inhibited the synthesis of vRNAs as well as the induction of MVP, both of which are critical components of Vaults as a drug transporter. Furthermore, we found that the synergistic effect of ECyd and CDDP was correlated with the MVP expression level when the effect was analyzed in additional cancer cell lines. Finally, we demonstrated that ECyd decreased the vRNAs expression level in xenograft tumor.
Our data indicated the ability of ECyd to cancel the resistance of cancer cells to CDDP by inhibiting the Vaults function and the decrease of Vaults expression itself, and the ability of the combination therapy with CDDP and ECyd to offer a new strategy for overcoming platinum resistance. Moreover, the study results suggest that Vaults could be a biomarker for stratifying patients who may benefit from the combination therapy with ECyd and platinum.
我们之前报道过,RNA聚合酶抑制剂3'-乙炔基胞苷(ECyd,TAS-106)在体外和体内肿瘤模型中均能增强铂类药物在多种肿瘤类型中的抗肿瘤疗效。然而,ECyd诱导疗效增强的分子机制仍不清楚。
通过逐步增加顺铂(CDDP)剂量建立耐顺铂的头颈癌KB细胞系。采用等效线图分析评估ECyd与CDDP的联合效应。使用实时PCR、免疫印迹分析和免疫细胞化学检测几种分子的转录和翻译后状态。采用异种移植试验来确认ECyd在体内增强CDDP抗肿瘤疗效的机制。
ECyd通过抑制药物转运体穹窿体复合物(穹窿体)使KB细胞对CDDP敏感。首先,我们发现穹窿体在耐CDDP的KB细胞中过表达。通过RNA干扰抑制主要穹窿蛋白(MVP)可恢复对CDDP的敏感性。接下来,我们发现与亲代配对细胞系相比,ECyd显著使耐药细胞对CDDP敏感。分子分析显示,ECyd抑制vRNA的合成以及MVP的诱导,这两者都是作为药物转运体的穹窿体的关键组成部分。此外,当在其他癌细胞系中分析这种效应时,我们发现ECyd与CDDP的协同效应与MVP表达水平相关。最后,我们证明ECyd降低了异种移植肿瘤中vRNA的表达水平。
我们的数据表明,ECyd能够通过抑制穹窿体功能和降低穹窿体自身表达来消除癌细胞对CDDP的耐药性,以及CDDP与ECyd联合治疗能够提供一种克服铂耐药性的新策略。此外,研究结果表明穹窿体可能是对ECyd与铂联合治疗可能受益的患者进行分层的生物标志物。