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解析人结直肠癌中靶向药物联合治疗耐药的机制。

Dissecting mechanisms of resistance to targeted drug combination therapy in human colorectal cancer.

机构信息

Cancer Research UK Cancer Therapeutics Unit, The Institute of Cancer Research, London, SM2 5NG, UK.

出版信息

Oncogene. 2019 Jun;38(25):5076-5090. doi: 10.1038/s41388-019-0780-z. Epub 2019 Mar 25.

Abstract

Genomic alterations in cancer cells result in vulnerabilities that clinicians can exploit using molecularly targeted drugs, guided by knowledge of the tumour genotype. However, the selective activity of these drugs exerts an evolutionary pressure on cancers that can result in the outgrowth of resistant clones. Use of rational drug combinations can overcome resistance to targeted drugs, but resistance may eventually develop to combinatorial therapies. We selected MAPK- and PI3K-pathway inhibition in colorectal cancer as a model system to dissect out mechanisms of resistance. We focused on these signalling pathways because they are frequently activated in colorectal tumours, have well-characterised mutations and are clinically relevant. By treating a panel of 47 human colorectal cancer cell lines with a combination of MEK- and PI3K-inhibitors, we observe a synergistic inhibition of growth in almost all cell lines. Cells with KRAS mutations are less sensitive to PI3K inhibition, but are particularly sensitive to the combined treatment. Colorectal cancer cell lines with inherent or acquired resistance to monotherapy do not show a synergistic response to the combination treatment. Cells that acquire resistance to an MEK-PI3K inhibitor combination treatment still respond to an ERK-PI3K inhibitor regimen, but subsequently also acquire resistance to this combination treatment. Importantly, the mechanisms of resistance to MEK and PI3K inhibitors observed, MEK1/2 mutation or loss of PTEN, are similar to those detected in the clinic. ERK inhibitors may have clinical utility in overcoming resistance to MEK inhibitor regimes; however, we find a recurrent active site mutation of ERK2 that drives resistance to ERK inhibitors in mono- or combined regimens, suggesting that resistance will remain a hurdle. Importantly, we find that the addition of low concentrations of the BCL2-family inhibitor navitoclax to the MEK-PI3K inhibitor regimen improves the synergistic interaction and blocks the acquisition of resistance.

摘要

癌细胞的基因组改变导致了一些缺陷,临床医生可以利用这些缺陷,通过对肿瘤基因型的了解,使用针对特定分子的药物进行治疗。然而,这些药物的选择性活性对癌症施加了一种进化压力,从而导致耐药克隆的生长。合理的药物组合的使用可以克服靶向药物的耐药性,但最终可能会对联合疗法产生耐药性。我们选择结直肠癌的 MAPK 和 PI3K 信号通路抑制作为一个模型系统,以剖析耐药的机制。我们关注这些信号通路是因为它们在结直肠肿瘤中经常被激活,具有特征明确的突变,并且具有临床相关性。通过用 MEK 和 PI3K 抑制剂联合处理一组 47 个人类结直肠癌细胞系,我们观察到几乎所有细胞系的生长都有协同抑制作用。具有 KRAS 突变的细胞对 PI3K 抑制的敏感性较低,但对联合治疗特别敏感。对单药治疗具有固有或获得性耐药的结直肠癌细胞系对联合治疗没有协同反应。对 MEK-PI3K 抑制剂联合治疗产生耐药性的细胞仍然对 ERK-PI3K 抑制剂方案有反应,但随后也对这种联合治疗产生耐药性。重要的是,观察到的对 MEK 和 PI3K 抑制剂的耐药机制,即 MEK1/2 突变或 PTEN 缺失,与在临床上检测到的相似。ERK 抑制剂在克服 MEK 抑制剂方案的耐药性方面可能具有临床应用价值;然而,我们发现 ERK2 的一个频繁发生的活性位点突变,它在单药或联合治疗中驱动了对 ERK 抑制剂的耐药性,这表明耐药性仍然是一个障碍。重要的是,我们发现将低浓度的 BCL2 家族抑制剂 navitoclax 加入 MEK-PI3K 抑制剂方案中可以改善协同作用并阻止耐药性的产生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef81/6755994/f81b5f229ec6/41388_2019_780_Fig1_HTML.jpg

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