DNA-PKcs抑制作为分化型甲状腺癌的治疗方法。

IF 4.6
Endocrine-related cancer Pub Date : 2025-07-30 Print Date: 2025-08-01 DOI:10.1530/ERC-25-0031
Shu-Fu Lin, Wei-Yi Chen, Chuen Hsueh, Ting-Chao Chou, Richard J Wong
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引用次数: 0

摘要

dna依赖性蛋白激酶催化亚基(DNA-PKcs)是一种丝氨酸-苏氨酸蛋白激酶,在癌症的基本细胞过程中起关键作用。DNA-PKcs可能是分化型甲状腺癌(DTC)治疗的潜在靶点。我们评估了DNA-PKcs抑制剂M3814在DTC治疗中的应用。M3814在四种DTC细胞系(TPC1、K1、FTC-133和FTC-238)中以剂量-反应方式引起细胞毒性。M3814诱导DTC细胞周期阻滞在S期。M3814单药治疗能够抑制K1肿瘤模型的生长。M3814联合lenvatinib在体外显示出协同作用,并且在FTC-133异种移植物模型中,该组合比任何单一治疗都更有效。这些结果表明,M3814在单独或联合治疗DTC方面具有显著的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
DNA-PKcs inhibition as a therapeutic approach for differentiated thyroid cancer.

DNA-dependent protein kinase catalytic subunit (DNA-PKcs) is a serine-threonine protein kinase that plays critical roles in cellular processes fundamental to cancer. DNA-PKcs may be a potential target for differentiated thyroid cancer (DTC) therapy. A DNA-PKcs inhibitor, M3814, was evaluated for its use in DTC therapy. M3814 caused cytotoxicity in a dose-response fashion in four DTC cell lines (TPC1, K1, FTC-133, and FTC-238). M3814 induced cell cycle arrest at the S phase in DTC cells. M3814 monotherapy was able to repress the growth of the K1 tumor model. M3814 in combination with lenvatinib demonstrated synergism in vitro, and this combination was more effective than any single therapy in an FTC-133 xenograft model. These results reveal that M3814 has significant potential in treating DTC, singly or in drug combination.

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