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Use of the γ-H2AX assay to monitor DNA damage and repair in translational cancer research

Cancer Letters · 2011 · Vol. 327(1-2) · pp. 123–133
Alesia IvashkevichChristophe E. RedonAsako NakamuraRoger F. MartinOlga A. Martin

Abstract

Formation of γ-H2AX in response to DNA double stranded breaks (DSBs) provides the basis for a sensitive assay of DNA damage in human biopsies. The review focuses on the application of γ-H2AX-based methods to translational studies to monitor the clinical response to DNA targeted therapies such as some forms of chemotherapy, external beam radiotherapy, radionuclide therapy or combinations thereof. The escalating attention on radiation biodosimetry has also highlighted the potential of the assay including renewed efforts to assess the radiosensitivity of prospective radiotherapy patients. Finally the γ-H2AX response has been suggested as a basis for an in vivo imaging modality.

DNA Repair MechanismsCancer therapeutics and mechanismsCarcinogens and Genotoxicity AssessmentBiodosimetryDNA damageRadiation therapyDNA repairRadiosensitivityCancer researchTranslational researchMedicineDNACancer

MeSH terms

AnimalsDNA DamageDNA RepairHistonesHumansNeoplasmsRadiation DosageRadiation ToleranceBiomarkers, TumorMolecular ImagingHigh-Throughput Screening AssaysTranslational Research, Biomedical

Funding

  • National Cancer Institute
  • National Institute of Allergy and Infectious Diseases
Citations
440
FWCI
5.72
field-weighted impact
References
150
Percentile
97%
vs. same field & year
Citations per year
Cited by
DNA Damage/Repair Management in Cancers
Cancers · 2020 · 338 citations
References
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