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LGR5 marks targetable tumor-initiating cells in mouse liver cancer

Author

Listed:
  • Wanlu Cao

    (Erasmus MC-University Medical Center)

  • Meng Li

    (Erasmus MC-University Medical Center)

  • Jiaye Liu

    (Erasmus MC-University Medical Center)

  • Shaoshi Zhang

    (Erasmus MC-University Medical Center)

  • Lisanne Noordam

    (Erasmus MC-University Medical Center)

  • Monique M. A. Verstegen

    (Erasmus MC-University Medical Center)

  • Ling Wang

    (Erasmus MC-University Medical Center)

  • Buyun Ma

    (Erasmus MC-University Medical Center)

  • Shan Li

    (Erasmus MC-University Medical Center)

  • Wenshi Wang

    (Erasmus MC-University Medical Center)

  • Michiel Bolkestein

    (Erasmus MC-University Medical Center
    Erasmus MC-University Medical Center)

  • Michael Doukas

    (Erasmus MC-University Medical Center)

  • Kan Chen

    (Erasmus MC-University Medical Center
    Northwest Minzu University
    Zhejiang Sci-Tech University)

  • Zhongren Ma

    (Northwest Minzu University)

  • Marco Bruno

    (Erasmus MC-University Medical Center)

  • Dave Sprengers

    (Erasmus MC-University Medical Center)

  • Jaap Kwekkeboom

    (Erasmus MC-University Medical Center)

  • Luc J. W. van der Laan

    (Erasmus MC-University Medical Center)

  • Ron Smits

    (Erasmus MC-University Medical Center)

  • Maikel P. Peppelenbosch

    (Erasmus MC-University Medical Center)

  • Qiuwei Pan

    (Erasmus MC-University Medical Center)

Abstract

Cancer stem cells (CSCs) or tumor-initiating cells (TICs) are thought to be the main drivers for disease progression and treatment resistance across various cancer types. Identifying and targeting these rare cancer cells, however, remains challenging with respect to therapeutic benefit. Here, we report the enrichment of LGR5 expressing cells, a well-recognized stem cell marker, in mouse liver tumors, and the upregulation of LGR5 expression in human hepatocellular carcinoma. Isolated LGR5 expressing cells from mouse liver tumors are superior in initiating organoids and forming tumors upon engraftment, featuring candidate TICs. These cells are resistant to conventional treatment including sorafenib and 5-FU. Importantly, LGR5 lineage ablation significantly inhibits organoid initiation and tumor growth. The combination of LGR5 ablation with 5-FU, but not sorafenib, further augments the therapeutic efficacy in vivo. Thus, we have identified the LGR5+ compartment as an important TIC population, representing a viable therapeutic target for combating liver cancer.

Suggested Citation

  • Wanlu Cao & Meng Li & Jiaye Liu & Shaoshi Zhang & Lisanne Noordam & Monique M. A. Verstegen & Ling Wang & Buyun Ma & Shan Li & Wenshi Wang & Michiel Bolkestein & Michael Doukas & Kan Chen & Zhongren M, 2020. "LGR5 marks targetable tumor-initiating cells in mouse liver cancer," Nature Communications, Nature, vol. 11(1), pages 1-16, December.
  • Handle: RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-15846-0
    DOI: 10.1038/s41467-020-15846-0
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