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双重 mTOR/DNA-PK 抑制剂 CC-115 诱导黑素瘤细胞死亡并具有放射增敏作用。

Dual mTOR/DNA-PK Inhibitor CC-115 Induces Cell Death in Melanoma Cells and Has Radiosensitizing Potential.

机构信息

Department of Radiation Oncology, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Universitätsstr. 27, 91054 Erlangen, Germany.

Department of Dermatology, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Ulmenweg 18, 91054 Erlangen, Germany.

出版信息

Int J Mol Sci. 2020 Dec 7;21(23):9321. doi: 10.3390/ijms21239321.

Abstract

CC-115 is a dual inhibitor of the mechanistic target of rapamycin (mTOR) kinase and the DNA-dependent protein kinase (DNA-PK) that is currently being studied in phase I/II clinical trials. DNA-PK is essential for the repair of DNA-double strand breaks (DSB). Radiotherapy is frequently used in the palliative treatment of metastatic melanoma patients and induces DSBs. Melanoma cell lines and healthy-donor skin fibroblast cell lines were treated with CC‑115 and ionizing irradiation (IR). Apoptosis, necrosis, and cell cycle distribution were analyzed. Colony forming assays were conducted to study radiosensitizing effects. Immunofluorescence microscopy was performed to determine the activity of homologous recombination (HR). In most of the malign cell lines, an increasing concentration of CC-115 resulted in increased cell death. Furthermore, strong cytotoxic effects were only observed in malignant cell lines. Regarding clonogenicity, all cell lines displayed decreased survival fractions during combined inhibitor and IR treatment and supra-additive effects of the combination were observable in 5 out of 9 melanoma cell lines. CC-115 showed radiosensitizing potential in 7 out of 9 melanoma cell lines, but not in healthy skin fibroblasts. Based on our data CC-115 treatment could be a promising approach for patients with metastatic melanoma, particularly in the combination with radiotherapy.

摘要

CC-115 是一种机械性靶标雷帕霉素激酶(mTOR)和 DNA 依赖性蛋白激酶(DNA-PK)的双重抑制剂,目前正在进行 I/II 期临床试验。DNA-PK 对于 DNA 双链断裂(DSB)的修复至关重要。放射疗法常用于转移性黑色素瘤患者的姑息治疗,并诱导 DSB。用 CC-115 和电离辐射(IR)处理黑色素瘤细胞系和健康供体皮肤成纤维细胞系。分析细胞凋亡、坏死和细胞周期分布。进行集落形成测定以研究放射增敏作用。进行免疫荧光显微镜检查以确定同源重组(HR)的活性。在大多数恶性细胞系中,CC-115 的浓度增加导致细胞死亡增加。此外,仅在恶性细胞系中观察到强烈的细胞毒性作用。关于集落形成能力,在联合抑制剂和 IR 处理期间,所有细胞系的存活分数均降低,并且在 9 个黑色素瘤细胞系中的 5 个中观察到联合作用的超相加效应。CC-115 在 9 个黑色素瘤细胞系中的 7 个中表现出放射增敏作用,但在健康皮肤成纤维细胞中没有。根据我们的数据,CC-115 治疗可能是转移性黑色素瘤患者的一种有前途的方法,特别是与放射疗法联合使用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d21e/7730287/027b438dd7eb/ijms-21-09321-g001.jpg

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