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Ageing limits stemness and tumorigenesis by reprogramming iron homeostasis.
- Source :
-
Nature [Nature] 2025 Jan; Vol. 637 (8044), pp. 184-194. Date of Electronic Publication: 2024 Dec 04. - Publication Year :
- 2025
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Abstract
- Ageing is associated with a decline in the number and fitness of adult stem cells <superscript>1,2</superscript> . Ageing-associated loss of stemness is posited to suppress tumorigenesis <superscript>3,4</superscript> , but this hypothesis has not been tested in vivo. Here we use physiologically aged autochthonous genetically engineered <superscript>5,6</superscript> mouse models and primary cells <superscript>5,6</superscript> to demonstrate that ageing suppresses lung cancer initiation and progression by degrading the stemness of the alveolar cell of origin. This phenotype is underpinned by the ageing-associated induction of the transcription factor NUPR1 and its downstream target lipocalin-2 in the cell of origin in mice and humans, which leads to functional iron insufficiency in the aged cells. Genetic inactivation of the NUPR1-lipocalin-2 axis or iron supplementation rescues stemness and promotes the tumorigenic potential of aged alveolar cells. Conversely, targeting the NUPR1-lipocalin-2 axis is detrimental to young alveolar cells through ferroptosis induction. Ageing-associated DNA hypomethylation at specific enhancer sites is associated with increased NUPR1 expression, which is recapitulated in young alveolar cells through DNA methylation inhibition. We uncover that ageing drives functional iron insufficiency that leads to loss of stemness and tumorigenesis but promotes resistance to ferroptosis. These findings have implications for the therapeutic modulation of cellular iron homeostasis in regenerative medicine and in cancer prevention. Furthermore, our findings are consistent with a model whereby most human cancers initiate at a young age, thereby highlighting the importance of directing cancer prevention efforts towards young individuals.<br />Competing Interests: Competing interests: T. Tammela is a scientific advisor with equity interests in Lime Therapeutics. His spouse is an employee of and has equity in Recursion Pharmaceuticals. The Tammela Laboratory receives funding from Ono Pharma unrelated to this work. E.S.W. has equity in and her spouse is a co-founder of and equity holder in Gertrude Biomedical Pty. The other authors declare no competing interests.<br /> (© 2024. The Author(s), under exclusive licence to Springer Nature Limited.)
- Subjects :
- Animals
Mice
Humans
Male
Female
Ferroptosis
Neoplasm Proteins metabolism
Neoplasm Proteins genetics
Alveolar Epithelial Cells metabolism
Alveolar Epithelial Cells pathology
Iron metabolism
Homeostasis
Aging metabolism
Carcinogenesis pathology
Carcinogenesis genetics
Carcinogenesis metabolism
DNA Methylation
Basic Helix-Loop-Helix Transcription Factors metabolism
Basic Helix-Loop-Helix Transcription Factors genetics
Lung Neoplasms pathology
Lung Neoplasms metabolism
Lung Neoplasms genetics
Lipocalin-2 metabolism
Lipocalin-2 genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1476-4687
- Volume :
- 637
- Issue :
- 8044
- Database :
- MEDLINE
- Journal :
- Nature
- Publication Type :
- Academic Journal
- Accession number :
- 39633048
- Full Text :
- https://doi.org/10.1038/s41586-024-08285-0