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依维莫司与吉非替尼在表皮生长因子受体酪氨酸激酶抑制剂耐药的非小细胞肺癌细胞系中具有协同作用。

Everolimus synergizes with gefitinib in non-small-cell lung cancer cell lines resistant to epidermal growth factor receptor tyrosine kinase inhibitors.

机构信息

Guangdong Lung Cancer Institute, Guangdong General Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China.

出版信息

Cancer Chemother Pharmacol. 2012 Nov;70(5):707-16. doi: 10.1007/s00280-012-1946-3. Epub 2012 Sep 2.

Abstract

PURPOSE

Epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI) therapy is considered as one of the most important treatments for patients with advanced non-small-cell lung cancer (NSCLC). However, not all patients benefit from this therapy because of primary or acquired resistance, both of which are usually caused by the activation of alternative signaling pathways. Thus, a combination of different signaling pathway inhibitors is a promising strategy. We used the mammalian target of rapamycin (mTOR) inhibitor everolimus in combination with gefitinib in NSCLC cell lines to analyze the efficacy of this combination regimen and the underlying molecular mechanism.

METHODS

Acquired gefitinib-resistant cell lines, together with EGFR wild-type and mutant primary gefitinib-resistant NSCLC cell lines, were treated with everolimus alone, gefitinib alone, or the combination of the two drugs, and the effects were evaluated using cell proliferation assays. The effects of everolimus and gefitinib on the EGFR pathway in NSCLC cell lines were determined by Western blot analysis.

RESULTS

Combined treatment resulted in synergistic antitumor effects in gefitinib-resistant cells A549 and H1975. The combination index (CI) of cells increased with increasing dose of everolimus. Everolimus demonstrated no apparent inhibition of phosphorylated Akt (p-Akt) and phosphorylated p44/42 MAPK (p-MAPK) in H1650 cells. Additionally, in gefitinib-resistant cell lines, the combination of gefitinib and everolimus not only showed stronger inhibition of phosphorylated mTOR and phosphorylated p70S6K expression than either drug alone but also reduced the levels of p-Akt and p-MAPK in both cell lines.

CONCLUSIONS

Our data showed that the combination of everolimus and gefitinib exhibits dose-dependent synergism in primary and acquired gefitinib-resistant NSCLC cells. Thus, a preclinical rationale exists for the use of everolimus to enhance the efficacy of gefitinib in EGFR-TKI-resistant patients with NSCLC.

摘要

目的

表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKI)治疗被认为是晚期非小细胞肺癌(NSCLC)患者的重要治疗方法之一。然而,由于原发性或获得性耐药,并非所有患者都能从中受益,这两种耐药通常是由替代信号通路的激活引起的。因此,联合使用不同信号通路抑制剂是一种很有前途的策略。我们使用哺乳动物雷帕霉素靶蛋白(mTOR)抑制剂依维莫司与吉非替尼联合用于 NSCLC 细胞系,以分析该联合方案的疗效及其潜在的分子机制。

方法

获得性吉非替尼耐药细胞系,以及 EGFR 野生型和突变型原发性吉非替尼耐药 NSCLC 细胞系,分别用依维莫司单药、吉非替尼单药或两药联合处理,用细胞增殖实验评估其疗效。用 Western blot 分析依维莫司和吉非替尼对 NSCLC 细胞系中 EGFR 通路的影响。

结果

联合治疗在吉非替尼耐药细胞 A549 和 H1975 中产生协同抗肿瘤作用。随着依维莫司剂量的增加,细胞的联合指数(CI)增加。依维莫司在 H1650 细胞中对磷酸化 Akt(p-Akt)和磷酸化 p44/42 MAPK(p-MAPK)无明显抑制作用。此外,在吉非替尼耐药细胞系中,吉非替尼和依维莫司联合治疗不仅比单药治疗更强地抑制磷酸化 mTOR 和磷酸化 p70S6K 的表达,而且还降低了两条细胞系中 p-Akt 和 p-MAPK 的水平。

结论

我们的数据表明,依维莫司和吉非替尼联合治疗在原发性和获得性吉非替尼耐药 NSCLC 细胞中具有剂量依赖性协同作用。因此,依维莫司增强 EGFR-TKI 耐药 NSCLC 患者吉非替尼疗效具有临床前依据。

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