Evidence map›Paper›PMID 38866739›Full record

ArticleCell death discovery2024

Inhibition of key DNA double strand break repair protein kinases enhances radiosensitivity of head and neck cancer cells to X-ray and proton irradiation.

Maria Rita Fabbrizi, Thomas J Doggett, Jonathan R Hughes, Emma Melia, Elizabeth R Dufficy, Rhianna M Hill, Amalia Goula, Ben Phoenix, Jason L Parsons

Abstract read
In one paragraph

Article in Cell death discovery, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Complete response in disseminatedTranslational lung cancer research · 2026
    Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Maria Rita FabbriziInstitute of Cancer and Genomic Sciences, University of Birmingham, Edgbaston, UK.ORCID http://orcid.org/0000-0002-5156-1575
Thomas J DoggettDepartment of Molecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, UK.
Jonathan R HughesInstitute of Cancer and Genomic Sciences, University of Birmingham, Edgbaston, UK.ORCID http://orcid.org/0000-0002-6420-2504
Emma MeliaInstitute of Cancer and Genomic Sciences, University of Birmingham, Edgbaston, UK.
Elizabeth R DufficyInstitute of Cancer and Genomic Sciences, University of Birmingham, Edgbaston, UK.
Rhianna M HillDepartment of Molecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, UK.
Amalia GoulaInstitute of Cancer and Genomic Sciences, University of Birmingham, Edgbaston, UK.
Ben PhoenixSchool of Physics and Astronomy, University of Birmingham, Edgbaston, UK.
Jason L ParsonsInstitute of Cancer and Genomic Sciences, University of Birmingham, Edgbaston, UK. j.parsons.3@bham.ac.uk.ORCID http://orcid.org/0000-0002-5052-1125

Funding

Realizing the radiobiological impact of protons and high-LET particles in head and neck cancer and glioblastoma modelsR01CA256854 · NCI · UNIVERSITY OF LIVERPOOL · PI PARSONS, JASON · 2021 to 2025
$1.7M
NCI NIH HHS R01 CA256854North West Cancer Research Fund (NWCR) CR1197RCUK | Medical Research Council (MRC) MR/V028944/1U.S. Department of Health & Human Services | National Institutes of Health (NIH) 1R01CA256854
6 · The paper itself

Abstract

Ionising radiation (IR) is widely used in cancer treatment, including for head and neck squamous cell carcinoma (HNSCC), where it induces significant DNA damage leading ultimately to tumour cell death. Among these lesions, DNA double strand breaks (DSBs) are the most threatening lesion to cell survival. The two main repair mechanisms that detect and repair DSBs are non-homologous end joining (NHEJ) and homologous recombination (HR). Among these pathways, the protein kinases ataxia telangiectasia mutated (ATM), ataxia telangiectasia and Rad3-related (ATR) and the DNA dependent protein kinase catalytic subunit (DNA-Pkcs) play key roles in the sensing of the DSB and subsequent coordination of the downstream repair events. Consequently, targeting these kinases with potent and specific inhibitors is considered an approach to enhance the radiosensitivity of tumour cells. Here, we have investigated the impact of inhibition of ATM, ATR and DNA-Pkcs on the survival and growth of six radioresistant HPV-negative HNSCC cell lines in combination with either X-ray irradiation or proton beam therapy, and confirmed the mechanistic pathway leading to cell radiosensitisation. Using inhibitors targeting ATM (AZD1390), ATR (AZD6738) and DNA-Pkcs (AZD7648), we observed that this led to significantly decreased clonogenic survival of HNSCC cell lines following both X-ray and proton irradiation. Radiosensitisation of HNSCC cells grown as 3D spheroids was also observed, particularly following ATM and DNA-Pkcs inhibition. We confirmed that the inhibitors in combination with X-rays and protons led to DSB persistence, and increased micronuclei formation. Cumulatively, our data suggest that targeting DSB repair, particularly via ATM and DNA-Pkcs inhibition, can exacerbate the impact of ionising radiation in sensitising HNSCC cell models.

Identifiers

PMID38866739
PMCPMC11169544

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.