Cited by 361DNA Repair MechanismsTelomeres, Telomerase, and SenescencePluripotent Stem Cells Research

DNA Damage in Stem Cells

Open access
Vitale, Ilio, Manic, Gwenola, De Maria, Ruggero, Kroemer, Guido, Galluzzi, Lorenzo·2017·Molecular Cell

Abstract

Both embryonic and adult stem cells are endowed with a superior capacity to prevent the accumulation of genetic lesions, repair them, or avoid their propagation to daughter cells, which would be particularly detrimental to the whole organism. Inducible pluripotent stem cells also display a robust DNA damage response, but the stability of their genome is often conditioned by the mutational history of the cell population of origin, which constitutes an obstacle to clinical applications. Cancer stem cells are particularly tolerant to DNA damage and fail to undergo senescence or regulated cell death upon accumulation of genetic lesions. Such a resistance contributes to the genetic drift of evolving tumors as well as to their limited sensitivity to chemo- and radiotherapy. Here, we discuss the pathophysiological and therapeutic implications of the molecular pathways through which stem cells cope with DNA damage.

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Crossref · 10.1016/j.molcel.2017.04.006

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  • Intrinsic apoptosis is initiated by microenvironmental perturbations including growth factor withdrawal, DNA damage, ER stress, ROS overload, replication stress, microtubular alterations or mitotic defects.

    “Intrinsic apoptosis is a form of RCD initiated by a variety of microenvironmental perturbations including (but not limited to) growth factor withdrawal, DNA damage, endoplasmic reticulum (ER) stress, reactive oxygen species (ROS) overload, replication stress, microtubular alterations or mitotic defects [29–34].”

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References 159 · Cited by 361

Authors
Vitale, I., Manic, G., De Maria, R., Kroemer, G., & Galluzzi, L.
Affiliations
  • University of Rome Tor Vergata (IT)
  • Karolinska University Hospital (SE)
  • Sorbonne Paris Cité (FR)
Corresponding author
  • Vitale, Ilio
  • Galluzzi, Lorenzo
Venue
Molecular Cell
Publisher
Elsevier BV
Published
2017-05
Volume
66
Issue
3
Pages
306-319
ISSN
1097-2765 (ISSN-L)
OpenAlex
W2611297475
Cited by
361
References
159
Citations by year
2026: 14 · 2025: 36 · 2024: 26 · 2023: 56 · 2022: 32 · 2021: 71 · 2020: 44 · 2019: 39 · 2018: 31 · 2017: 11
FWCI
3.20
Type
journal article
Language
en
Open access
Locations
  • Molecular Cell (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • European Commission
  • Labex Immuno-Oncology
  • Ligue Contre le Cancer
  • European Research Council
  • Amaldi Research Center
  • Institut Universitaire de France
  • Agence Nationale de la Recherche
  • Associazione Italiana per la Ricerca sul Cancro (14641)
  • Fondation Leducq
  • Institut National Du Cancer
  • West Coast Metabolomics Center, University of California, Davis
  • Cancéropôle Ile de France
  • Ministero della Salute (9979, RF_GR-2011-02351355)
  • Association pour la Recherche sur le Cancer
  • Fondation pour la Recherche Médicale
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
  • Health Sciences › Medicine › Physiology › Telomeres, Telomerase, and Senescence
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Pluripotent Stem Cells Research
Keywords
DNA damage response, stem cells, embryonic stem cells, adult stem cells, induced pluripotent stem cells, cancer stem cells, genome stability, DNA repair, senescence resistance
MeSH terms
Animals, DNA Damage, DNA Repair, Humans, Mutation, Neoplasms, Radiation Tolerance, Neoplastic Stem Cells, Pluripotent Stem Cells, Genetic Drift, Genomic Instability, Embryonic Stem Cells, Adult Stem Cells

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