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首页> 外文期刊>Cell death & disease. >A patient-derived xenograft pre-clinical trial reveals treatment responses and a resistance mechanism to karonudib in metastatic melanoma
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A patient-derived xenograft pre-clinical trial reveals treatment responses and a resistance mechanism to karonudib in metastatic melanoma

机译:患者衍生的异种移植前临床试验显示治疗反应和转移黑素瘤的karonudib的抗性机制

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Karonudib (TH1579) is a novel compound that exerts anti-tumor activities and has recently entered phase I clinical testing. The aim of this study was to conduct a pre-clinical trial in patient-derived xenografts to identify the possible biomarkers of response or resistance that could guide inclusion of patients suffering from metastatic melanoma in phase II clinical trials. Patient-derived xenografts from 31 melanoma patients with metastatic disease were treated with karonudib or a vehicle for 18 days. Treatment responses were followed by measuring tumor sizes, and the models were categorized in the response groups. Tumors were harvested and processed for RNA sequencing and protein analysis. To investigate the effect of karonudib on T-cell-mediated anti-tumor activities, tumor-infiltrating T cells were injected in mice carrying autologous tumors and the mice treated with karonudib. We show that karonudib has heterogeneous anti-tumor effect on metastatic melanoma. Thus, based on the treatment responses, we could divide the 31 patient-derived xenografts in three treatment groups: progression group (32%), suppression group (42%), and regression group (26%). Furthermore, we show that karonudib has anti-tumor effect, irrespective of major melanoma driver mutations. Also, we identify high expression of ABCB1, which codes for p-gp pumps as a resistance biomarker. Finally, we show that karonudib treatment does not hamper T-cell-mediated anti-tumor responses. These findings can be used to guide future use of karonudib in clinical use with a potential approach as precision medicine.
机译:Karonudib(TH1579)是一种新化合物,施加抗肿瘤活动,最近进入I阶段临床测试。本研究的目的是在患者衍生的异种移植物中进行临床前试验,以确定可能导致患有II期临床试验中患有转移性黑素瘤的患者的响应或抗性的可能生物标志物。从31例转移性疾病患者的患者衍生的异种移植物用karonudib或载体处理18天。然后通过测量肿瘤尺寸,并将模型分类在响应组中。收获肿瘤并加工用于RNA测序和蛋白质分析。为了研究Karonudib对T细胞介导的抗肿瘤活性的影响,将肿瘤渗透T细胞注射携带自体肿瘤的小鼠和用karonudib处理的小鼠。我们表明Karonudib对转移性黑色素瘤具有异质的抗肿瘤作用。因此,基于治疗反应,我们可以将31只患者衍生的异种移植物分为三个治疗组:进展组(32%),抑制基团(42%)和回归组(26%)。此外,我们表明Karonudib具有抗肿瘤效果,无论是主要的黑色素瘤驱动器突变如何。此外,我们鉴定了ABCB1的高表达,其作为电阻生物标志物的P-GP泵代码。最后,我们表明Karonudib治疗不会阻碍T细胞介导的抗肿瘤反应。这些发现可用于引导将来在临床上使用Karonudib,以潜在的方法作为精确药物。

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