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环孢素 A 通过抑制 Ca2+/钙调神经磷酸酶/ERK 通路使肺癌细胞对克唑替尼敏感。

Cyclosporine A sensitizes lung cancer cells to crizotinib through inhibition of the Ca2/calcineurin/Erk pathway.

机构信息

Department of Medical Oncology, Sir Run Run Shaw Hospital, College of Medicine, Zhejiang University, Zhejiang, Hangzhou, China.

Laboratory of Cancer Biology, Institute of Clinical Science, Sir Run Run Shaw Hospital, College of Medicine, Zhejiang University, Zhejiang, Hangzhou, China.

出版信息

EBioMedicine. 2019 Apr;42:326-339. doi: 10.1016/j.ebiom.2019.03.019. Epub 2019 Mar 15.

Abstract

BACKGROUND

Crizotinib has potent anti-tumor activity in patients with advanced MET-amplified non-small cell lung cancer (NSCLC). However, the therapeutic effect is still not satisfying. Thus, developing approaches that improve the efficacy of crizotinib remains a significant challenge.

METHODS

MET-amplified NSCLC cell lines were treated with crizotinib and cyclosporine A (CsA). Cell viability was determined by MTS assay. The changes of apoptosis, cell cycle and calcineurin-Erk pathways were assessed by western blot. Xenograft mouse model, primary human NSCLC cells and hollow fiber assays were utilized to confirm the effects of CsA.

FINDINGS

We demonstrated that CsA significantly increased the anti-tumor effect of crizotinib on multiple MET-amplified NSCLC cells in vitro and in vivo. Mechanistically, crizotinib treatment led to the activation of Ca-calcineurin (CaN)-Kinase suppressor of Ras 2 (KSR2) signaling, resulting in Erk1/2 activation and enhanced survival of cancer cells. CsA effectively blocked CaN-KSR2-Erk1/2 signaling, promoting crizotinib-induced apoptosis and G2/M arrest. Similarly, pharmacologic or genetic inhibition of Erk1/2 also enhanced crizotinib-induced growth inhibition in vitro. Xenograft studies further confirmed that CsA or Erk1/2 inhibitor PD98059 enhanced the anti-cancer activity of crizotinib through inhibition of CaN-Erk1/2 axis. The results were also validated by primary human NSCLC cells in vitro and hollow fiber assays in vivo.

INTERPRETATION

This study provides preclinical evidences that combination therapy of CsA and crizotinib is a promising approach for targeted treatment of MET-amplified lung cancer patients. FUND: This work was supported by the National Natural Science Foundation of China, the Key Projects of Natural Foundation of Zhejiang Province, the Ten thousand plan youth talent support program of Zhejiang Province, the Zhejiang Natural Sciences Foundation Grant, and the Zhejiang medical innovative discipline construction project-2016.

摘要

背景

克唑替尼对 MET 扩增的晚期非小细胞肺癌(NSCLC)患者具有强大的抗肿瘤活性。然而,治疗效果仍不尽人意。因此,开发提高克唑替尼疗效的方法仍然是一个重大挑战。

方法

用克唑替尼和环孢素 A(CsA)处理 MET 扩增的 NSCLC 细胞系。通过 MTS 测定法测定细胞活力。通过 Western blot 评估细胞凋亡、细胞周期和钙调神经磷酸酶-Erk 通路的变化。利用异种移植小鼠模型、原代人 NSCLC 细胞和中空纤维测定法来证实 CsA 的作用。

发现

我们证明 CsA 显著增强了克唑替尼在体外和体内对多种 MET 扩增的 NSCLC 细胞的抗肿瘤作用。从机制上讲,克唑替尼治疗导致 Ca-钙调神经磷酸酶(CaN)-KSR2 信号的激活,从而导致 Erk1/2 的激活和癌细胞的存活增强。CsA 有效地阻断 CaN-KSR2-Erk1/2 信号通路,促进克唑替尼诱导的细胞凋亡和 G2/M 期阻滞。同样,体外药理学或基因抑制 Erk1/2 也增强了克唑替尼诱导的生长抑制作用。异种移植研究进一步证实,CsA 或 Erk1/2 抑制剂 PD98059 通过抑制 CaN-Erk1/2 轴增强了克唑替尼的抗癌活性。该结果还通过体外原代人 NSCLC 细胞和体内中空纤维测定法进行了验证。

解释

这项研究提供了临床前证据,表明 CsA 和克唑替尼联合治疗是一种有前途的针对 MET 扩增肺癌患者的靶向治疗方法。

基金

本工作得到国家自然科学基金、浙江省自然科学基金重点项目、浙江省万人计划青年人才支持计划、浙江省自然科学基金资助、浙江省医学创新学科建设项目-2016 年的支持。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7606/6491942/1d1b5d03ce1e/gr1.jpg

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