生物
免疫检查点
免疫系统
衰老
癌症研究
趋化因子
细胞周期
表型
免疫疗法
免疫学
细胞
细胞生物学
基因
遗传学
作者
Tomoko Morita,Jie Yu,Yukie Kashima,Ryo Kamata,Go Yamamoto,Tatsunori Minamide,Chiaki Mashima,Miyuki Yoshiya,Yuta Sakae,Toyohiro Yamauchi,Yumi Hakozaki,Shun‐Ichiro Kageyama,Akira Nakamura,Eric S. Lightcap,Kosuke Tanaka,Huifeng Niu,Karuppiah Kannan,Akihiro Ohashi
标识
DOI:10.1038/s41467-023-43274-3
摘要
Serine/threonine kinase, cell division cycle 7 (CDC7) is critical for initiating DNA replication. TAK-931 is a specific CDC7 inhibitor, which is a next-generation replication stress (RS) inducer. This study preclinically investigates TAK-931 antitumor efficacy and immunity regulation. TAK-931 induce RS, generating senescence-like aneuploid cells, which highly expressed inflammatory cytokines and chemokines (senescence-associated secretory phenotype, SASP). In vivo multilayer-omics analyses in gene expression panel, immune panel, immunohistochemistry, RNA sequencing, and single-cell RNA sequencing reveal that the RS-mediated aneuploid cells generated by TAK-931 intensively activate inflammatory-related and senescence-associated pathways, resulting in accumulation of tumor-infiltrating immune cells and potent antitumor immunity and efficacy. Finally, the combination of TAK-931 and immune checkpoint inhibitors profoundly enhance antiproliferative activities. These findings suggest that TAK-931 has therapeutic antitumor properties and improved clinical benefits in combination with conventional immunotherapy.
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