Author
Listed:
- Kazutaka Nakamura
(The University of Tokyo
The University of Tokyo)
- Masayuki Tsukasaki
(The University of Tokyo)
- Takaaki Tsunematsu
(Tokushima University Graduate School of Biomedical Sciences)
- Minglu Yan
(The University of Tokyo
University of Texas Southwestern Medical Center)
- Yutaro Ando
(The University of Tokyo)
- Nam Cong-Nhat Huynh
(University of Medicine and Pharmacy at Ho Chi Minh City)
- Kyoko Hashimoto
(The University of Tokyo)
- Qiao Gou
(The University of Tokyo)
- Ryunosuke Muro
(The University of Tokyo
Tokyo University of Science)
- Ayumi Itabashi
(The University of Tokyo)
- Takahiro Iguchi
(The University of Tokyo)
- Kazuo Okamoto
(The University of Tokyo
Kanazawa University)
- Takashi Nakamura
(Tokyo Dental College)
- Kenta Nakano
(National Center for Global Health and Medicine)
- Tadashi Okamura
(National Center for Global Health and Medicine)
- Tomoya Ueno
(Nagasaki University)
- Kosei Ito
(Nagasaki University)
- Naozumi Ishimaru
(Tokyo Medical and Dental University)
- Kazuto Hoshi
(The University of Tokyo)
- Hiroshi Takayanagi
(The University of Tokyo)
Abstract
The periosteum is the layer of cells that covers nearly the entire surface of every bone. Upon infection, injury or malignancy the bone surface undergoes new growth—the periosteal reaction—but the mechanism and physiological role of this process remain unknown1,2. Here we show that the periosteal reaction protects against cancer invasion into the bone. Histological analyses of human lesions of head and neck squamous cell carcinomas (HNSCCs) show that periosteal thickening occurs in proximity to the tumour. We developed a genetically dissectible mouse model of HNSCC and demonstrate that inducible depletion of periosteal cells accelerates cancerous invasion of the bone. Single-cell RNA sequencing reveals that expression of the gene encoding the protease inhibitor TIMP1 is markedly increased in the periosteum at the pre-invasive stage. This increase is due to upregulation of HIF1α expression in the tumour microenvironment, and increased TIMP1 inactivates matrix-degrading proteases, promoting periosteal thickening to inhibit cancer invasion. Genetic deletion of Timp1 impairs periosteal expansion, exacerbating bone invasion and decreasing survival in tumour-bearing mice. Together, these data show that the periosteal reaction may act as a functional stromal barrier against tumour progression, representing a unique example of tissue immunity mediated by stromal cells.
Suggested Citation
Kazutaka Nakamura & Masayuki Tsukasaki & Takaaki Tsunematsu & Minglu Yan & Yutaro Ando & Nam Cong-Nhat Huynh & Kyoko Hashimoto & Qiao Gou & Ryunosuke Muro & Ayumi Itabashi & Takahiro Iguchi & Kazuo Ok, 2024.
"The periosteum provides a stromal defence against cancer invasion into the bone,"
Nature, Nature, vol. 634(8033), pages 474-481, October.
Handle:
RePEc:nat:nature:v:634:y:2024:i:8033:d:10.1038_s41586-024-07822-1
DOI: 10.1038/s41586-024-07822-1
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