Meng Jiao, Chang Cuicui, Chen Yuhua, Bi Fangfang, Ji Chen, Liu Wei
Central Laboratory of Medicine School, Xi'an Peihua University, Xi'an 710100, People's Republic of China.
Department of Medical Science Research Center, Shaanxi Fourth People's Hospital, Xi'an 710143, People's Republic of China.
Onco Targets Ther. 2019 Jul 26;12:6033-6043. doi: 10.2147/OTT.S209441. eCollection 2019.
Several EGFR-tyrosine kinase inhibitors (TKIs), such as gefitinib (Gef), have been used as effective clinical therapies for patients with non-small cell lung cancer (NSCLC). However, due to acquired resistance, the efficacy of Gef treatment is severely blocked. Our preliminary study found that epigallocatechin gallate (EGCG) in combination with Gef could work synergistically to increase the sensitivity to Gef in NSCLC, but the mechanisms responsible for this have not been completely defined.
In our present study, we devoted to investigate the synergistic effects of combined EGCG and Gef treatment and the importance of autophagy and ERK signaling pathway in overcoming acquired drug resistance to Gef in NSCLC.
We evaluated the synergistic effects of combined EGCG and Gef treatment through in vitro cell proliferation/viability assays and in vivo xenograft studies, respectively. Autophagic flux was assessed by GFP-microtubule-associated protein 1 light chain 3 (LC3) plasmid transfection and western blot detection of autophagy-related proteins. Besides, the role of ERK on acquired resistance was validated with a ERK inhibitor.
We discovered that EGCG can synergize with Gef to inhibit the proliferation of Gef-resistant NSCLC cells and suppress tumor growth in a xenograft mouse model. The underlying mechanisms of synergism were investigated, and the results showed that co-treatment with Gef and EGCG could inhibit Gef-induced autophagy and ERK phosphorylation. Consistently, the expression of LC3-II/I and ATG5 were inhibited, whereas the expression of p62 was enhanced in EGCG and Gef combination treatment groups. Further, inhibition of autophagy in Gef-resistant A549 cells could augment cell death.
In conclusion, EGCG overcomes Gef resistance by inhibiting autophagy and augmenting cell death through targeting ERK pathway in NSCLC. Gef and EGCG combination therapy may be an effective strategy to overcome acquired resistance in NSCLC.
几种表皮生长因子受体-酪氨酸激酶抑制剂(TKIs),如吉非替尼(Gef),已被用作非小细胞肺癌(NSCLC)患者的有效临床治疗药物。然而,由于获得性耐药,吉非替尼治疗的疗效受到严重阻碍。我们的初步研究发现,表没食子儿茶素没食子酸酯(EGCG)与吉非替尼联合使用可协同作用,提高NSCLC对吉非替尼的敏感性,但其作用机制尚未完全明确。
在本研究中,我们致力于探讨EGCG与吉非替尼联合治疗的协同作用,以及自噬和ERK信号通路在克服NSCLC对吉非替尼获得性耐药中的重要性。
我们分别通过体外细胞增殖/活力测定和体内异种移植研究评估了EGCG与吉非替尼联合治疗的协同作用。通过绿色荧光蛋白-微管相关蛋白1轻链3(LC3)质粒转染和自噬相关蛋白的蛋白质印迹检测来评估自噬通量。此外,用ERK抑制剂验证了ERK在获得性耐药中的作用。
我们发现EGCG可与吉非替尼协同抑制吉非替尼耐药的NSCLC细胞增殖,并在异种移植小鼠模型中抑制肿瘤生长。研究了协同作用的潜在机制,结果表明,吉非替尼与EGCG联合治疗可抑制吉非替尼诱导的自噬和ERK磷酸化。一致地,在EGCG与吉非替尼联合治疗组中,LC3-II/I和ATG5的表达受到抑制,而p62的表达增强。此外,抑制吉非替尼耐药的A549细胞中的自噬可增加细胞死亡。
总之,EGCG通过抑制自噬并通过靶向NSCLC中的ERK途径增加细胞死亡来克服吉非替尼耐药。吉非替尼与EGCG联合治疗可能是克服NSCLC获得性耐药的有效策略。