Department of Pharmacology & Toxicology, Otago School of Biomedical Sciences, University of Otago, Dunedin, New Zealand.
Sci Rep. 2017 Oct 24;7(1):13955. doi: 10.1038/s41598-017-14289-w.
ALK positive non-small cell lung cancer is highly responsive to ALK inhibitors such as crizotinib, but drug resistance typically develops within a year of treatment. In this study we investigated whether IGF-1R is an independent druggable target in ALK-positive lung cancer cells. We confirmed that combination ALK and IGF-1R inhibitor treatment is synergistically cytotoxic to ALK-positive lung cancer cells and that this remains the case for at least 12 days after initial exposure to crizotinib. ALK-positive cells with acquired resistance to crizotinib did not acquire cross-resistance to IGF-1R inhibition, though combination treatment in the resistant cells gave additive rather than synergistic cytotoxicity. We concluded that IGF-1R is an independent druggable target in ALK-positive lung cancer and support the trial of combination treatment.
间变性淋巴瘤激酶阳性非小细胞肺癌对间变性淋巴瘤激酶抑制剂(如克唑替尼)高度敏感,但在治疗后一年内通常会产生耐药性。在这项研究中,我们研究了 IGF-1R 是否是间变性淋巴瘤激酶阳性肺癌细胞中独立的可用药靶点。我们证实,ALK 和 IGF-1R 抑制剂联合治疗对间变性淋巴瘤激酶阳性肺癌细胞具有协同细胞毒性作用,并且在初始接触克唑替尼后至少 12 天内仍然如此。对克唑替尼获得耐药性的ALK 阳性细胞并未对 IGF-1R 抑制产生交叉耐药性,尽管在耐药细胞中联合治疗具有相加而非协同的细胞毒性作用。我们得出结论,IGF-1R 是间变性淋巴瘤激酶阳性肺癌的一个独立的可用药靶点,并支持联合治疗的试验。