Wu Min, Yuan Yuan, Pan Yue-Yin, Zhang Ying
Department of Geriatrics, The Third Affiliated Hospital of Anhui Medical University, Hefei, Anhui 230061, P.R. China.
The Central Laboratory of Binhu Hospital, The Third Affiliated Hospital of Anhui Medical University, Hefei, Anhui 230061, P.R. China.
Mol Med Rep. 2014 Aug;10(2):931-8. doi: 10.3892/mmr.2014.2243. Epub 2014 May 16.
Currently, chemotherapy and targeted therapies share the principal limitation of the emergence of drug resistance, which prevents these strategies from having lasting clinical benefits. The combination of epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) with concurrent chemotherapy has been proposed as one strategy to overcome acquired resistance to EGFR-TKIs. The purpose of the present study was to investigate the combined effects of gefitinib and pemetrexed on EGFR-TKI-sensitive and EGFR‑TKI‑resistant human non-small cell lung cancer (NSCLC) cell lines. The antiproliferative effects of gefitinib and pemetrexed, alone and in combination, on the growth of NSCLC cell lines, were assessed using an MTT assay. The cytotoxic interaction between the two drugs was evaluated in vitro using the combination index (CI) method. Cell cycle distribution and apoptosis were analyzed by flow cytometry and alterations in signaling pathways were determined by western blot analysis. In the present study, it was identified that when cells were concurrently exposed to pemetrexed and gefitinib, cytotoxic synergism was present in the gefitinib-resistant PC9/GR human NSCLC cell line and antagonistic interactions were observed in the gefitinib-sensitive PC9 cell line. Synergism was associated with a combination of cell cycle effects of the different agents. In addition, the combination of pemetrexed and gefitinib decreased the levels of phosphorylated AKT, phosphorylated extracellular-signal-regulated kinase and B-cell lymphoma 2 as compared with those in the control. By contrast, antagonism was associated with gefitinib-induced G0/G1-phase blockade of gefitinib-sensitive cells, which interfered with the cell cycle-specific cytotoxicity of chemotherapy. The combination of pemetrexed and gefitinib generated synergistic effects in gefitinib-acquired resistant cells and antagonistic effects in gefitinib-sensitive cells, suggesting that EGFR-TKIs combined with pemetrexed may be a beneficial treatment strategy for NSCLC patients with acquired resistance to EGFR-TKIs.
目前,化疗和靶向治疗都存在耐药性出现这一主要局限性,这使得这些治疗策略无法产生持久的临床益处。表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKIs)与同步化疗联合应用已被提出作为克服对EGFR-TKIs获得性耐药的一种策略。本研究的目的是探讨吉非替尼和培美曲塞对EGFR-TKI敏感和EGFR-TKI耐药的人非小细胞肺癌(NSCLC)细胞系的联合作用。采用MTT法评估吉非替尼和培美曲塞单独及联合应用对NSCLC细胞系生长的抗增殖作用。使用联合指数(CI)法在体外评估两种药物之间的细胞毒性相互作用。通过流式细胞术分析细胞周期分布和凋亡情况,并通过蛋白质印迹分析确定信号通路的变化。在本研究中,发现当细胞同时暴露于培美曲塞和吉非替尼时,吉非替尼耐药的PC9/GR人NSCLC细胞系中存在细胞毒性协同作用,而在吉非替尼敏感的PC9细胞系中观察到拮抗相互作用。协同作用与不同药物的细胞周期效应组合有关。此外,与对照组相比,培美曲塞和吉非替尼联合应用降低了磷酸化AKT、磷酸化细胞外信号调节激酶和B细胞淋巴瘤2的水平。相比之下,拮抗作用与吉非替尼诱导的吉非替尼敏感细胞的G0/G1期阻滞有关,这干扰了化疗的细胞周期特异性细胞毒性。培美曲塞和吉非替尼联合应用在吉非替尼获得性耐药细胞中产生协同作用,在吉非替尼敏感细胞中产生拮抗作用,表明EGFR-TKIs与培美曲塞联合应用可能是对EGFR-TKIs获得性耐药的NSCLC患者有益的治疗策略。