多路复用
癌症
癌症研究
乳腺癌
医学
免疫疗法
体内
全景望远镜
癌细胞
三阴性乳腺癌
肿瘤科
生物
内科学
生物信息学
生物化学
生物技术
组蛋白脱乙酰基酶
基因
组蛋白
作者
Zuzana Tatárová,Dylan C. Blumberg,James E. Korkola,Laura M. Heiser,John Muschler,Pepper Schedin,Sebastian W. Ahn,Gordon B. Mills,Lisa M. Coussens,Oliver Jonas,Joe W. Gray
标识
DOI:10.1038/s41587-022-01379-y
摘要
Systematically identifying synergistic combinations of targeted agents and immunotherapies for cancer treatments remains difficult. In this study, we integrated high-throughput and high-content techniques-an implantable microdevice to administer multiple drugs into different sites in tumors at nanodoses and multiplexed imaging of tumor microenvironmental states-to investigate the tumor cell and immunological response signatures to different treatment regimens. Using a mouse model of breast cancer, we identified effective combinations from among numerous agents within days. In vivo studies in three immunocompetent mammary carcinoma models demonstrated that the predicted combinations synergistically increased therapeutic efficacy. We identified at least five promising treatment strategies, of which the panobinostat, venetoclax and anti-CD40 triple therapy was the most effective in inducing complete tumor remission across models. Successful drug combinations increased spatial association of cancer stem cells with dendritic cells during immunogenic cell death, suggesting this as an important mechanism of action in long-term breast cancer control.
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