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CDC7 inhibition induces replication stress-mediated aneuploid cells with an inflammatory phenotype sensitizing tumors to immune checkpoint blockade

Author

Listed:
  • Tomoko Yamamori Morita

    (Exploratory Oncology Research & Clinical Trial Center, National Cancer Center)

  • Jie Yu

    (Oncology Drug Discovery Unit, Takeda Development Center Americas (TDCA), Inc.)

  • Yukie Kashima

    (Exploratory Oncology Research & Clinical Trial Center, National Cancer Center
    The University of Tokyo)

  • Ryo Kamata

    (Exploratory Oncology Research & Clinical Trial Center, National Cancer Center)

  • Gaku Yamamoto

    (Exploratory Oncology Research & Clinical Trial Center, National Cancer Center)

  • Tatsunori Minamide

    (Exploratory Oncology Research & Clinical Trial Center, National Cancer Center
    National Cancer Center Hospital East)

  • Chiaki Mashima

    (Exploratory Oncology Research & Clinical Trial Center, National Cancer Center)

  • Miyuki Yoshiya

    (Exploratory Oncology Research & Clinical Trial Center, National Cancer Center)

  • Yuta Sakae

    (Exploratory Oncology Research & Clinical Trial Center, National Cancer Center)

  • Toyohiro Yamauchi

    (Exploratory Oncology Research & Clinical Trial Center, National Cancer Center
    The University of Tokyo)

  • Yumi Hakozaki

    (Exploratory Oncology Research & Clinical Trial Center, National Cancer Center)

  • Shun-ichiro Kageyama

    (National Cancer Center Hospital East)

  • Akito Nakamura

    (Oncology Drug Discovery Unit, Takeda Development Center Americas (TDCA), Inc.)

  • Eric Lightcap

    (Oncology Drug Discovery Unit, Takeda Development Center Americas (TDCA), Inc.)

  • Kosuke Tanaka

    (Exploratory Oncology Research & Clinical Trial Center, National Cancer Center)

  • Huifeng Niu

    (Oncology Translational Science., TDCA, Inc.)

  • Karuppiah Kannan

    (Oncology Therapeutic Area Unit, TDCA, Inc.)

  • Akihiro Ohashi

    (Exploratory Oncology Research & Clinical Trial Center, National Cancer Center
    Oncology Drug Discovery Unit, Takeda Development Center Americas (TDCA), Inc.
    The University of Tokyo)

Abstract

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.

Suggested Citation

  • Tomoko Yamamori Morita & Jie Yu & Yukie Kashima & Ryo Kamata & Gaku Yamamoto & Tatsunori Minamide & Chiaki Mashima & Miyuki Yoshiya & Yuta Sakae & Toyohiro Yamauchi & Yumi Hakozaki & Shun-ichiro Kagey, 2023. "CDC7 inhibition induces replication stress-mediated aneuploid cells with an inflammatory phenotype sensitizing tumors to immune checkpoint blockade," Nature Communications, Nature, vol. 14(1), pages 1-21, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-43274-3
    DOI: 10.1038/s41467-023-43274-3
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