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淫羊藿提取物与吉非替尼联合治疗克服非小细胞肺癌细胞中T790M突变引起的耐药性。

Combined treatment with Epimedium koreanum Nakai extract and gefitinib overcomes drug resistance caused by T790M mutation in non-small cell lung cancer cells.

作者信息

Song Jie, Zhong Rongling, Huang Houcai, Zhang Zhenhai, Ding Dongmei, Yan Hongmei, Sun E, Jia Xiaobin

机构信息

a Key Laboratory of Delivery Systems of Chinese Meteria Medica , Jiangsu Provincial Academy of Chinese Medicine , Jiangsu , Nanjing , China.

出版信息

Nutr Cancer. 2014;66(4):682-9. doi: 10.1080/01635581.2014.895392. Epub 2014 Apr 16.

Abstract

Although the epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors, such as gefitinib, have shown promising therapeutic efficacy in nonsmall cell lung cancer (NSCLC) patients harboring EGFR activating mutation, development of acquired resistance is almost inevitable. We investigated whether the addition of Epimedium koreanum Nakai extract (EEF) to gefitinib could overcome the resistance of NSCLC cells to gefitinib. In our study, the growth inhibitory effects of cotreatment differed between mutant EGFR and wild type EGFR. A synergistic antiproliferative effect was observed in the combined treatments in H1975 and PC-9GR cells carrying T790M EGFR. In addition, the cotreatment exhibited a much greater inhibition than either agent alone on the following metastatic processes: (a) invasion, (b) wound healing, and (c) tubule formation by endothelial cells. The phosphorylations of EGFR family (EGFR, HER-2, and HER-3) and EGFR downstream PI3K/Akt/mTOR pathway in H1975 and PC-9/GR cells were also attanuated, whereas EEF or gefitinib alone had no obvious effects. Similarly, the combination effectively suppressed tumor growth and increased mice survival in PC-9GR xenografts. The results indicate that the addition of EEF to gefitinib is a promising strategy to overcome T790M-mediated drug resistance.

摘要

尽管表皮生长因子受体(EGFR)酪氨酸激酶抑制剂,如吉非替尼,在携带EGFR激活突变的非小细胞肺癌(NSCLC)患者中已显示出有前景的治疗效果,但获得性耐药的发生几乎不可避免。我们研究了在吉非替尼中添加朝鲜淫羊藿提取物(EEF)是否能克服NSCLC细胞对吉非替尼的耐药性。在我们的研究中,联合治疗的生长抑制作用在突变型EGFR和野生型EGFR之间有所不同。在携带T790M EGFR的H1975和PC-9GR细胞的联合治疗中观察到协同的抗增殖作用。此外,联合治疗在以下转移过程中表现出比单独使用任何一种药物更强的抑制作用:(a)侵袭,(b)伤口愈合,以及(c)内皮细胞形成小管。H1975和PC-9/GR细胞中EGFR家族(EGFR、HER-2和HER-3)的磷酸化以及EGFR下游PI3K/Akt/mTOR通路也被减弱,而单独使用EEF或吉非替尼则没有明显效果。同样,在PC-9GR异种移植瘤中,联合治疗有效地抑制了肿瘤生长并延长了小鼠存活时间。结果表明,在吉非替尼中添加EEF是克服T790M介导的耐药性的一种有前景的策略。

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