Evidence map›Paper›PMID 38014593›Full record

ArticleRadiation research2023

Effects of Differing Underlying Assumptions in In Silico Models on Predictions of DNA Damage and Repair.

John W Warmenhoven, Nicholas T Henthorn, Aimee L McNamara, Samuel P Ingram, Michael J Merchant, Karen J Kirkby, Jan Schuemann, Harald Paganetti, Kevin M Prise, Stephen J McMahon

Open access · greenAbstract read
In one paragraph

Article in Radiation research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
1.6field-weighted citation impact, top 15% of its field
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

0 citing papers in PubMed, 6 citations in OpenAlex.

No citing paper in PubMed yet.

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

10 authors at 7 institutions in 2 countries.

John W WarmenhovenDivision of Cancer Sciences, University of Manchester, Manchester, United Kingdom.
Nicholas T HenthornDivision of Cancer Sciences, University of Manchester, Manchester, United Kingdom.
Aimee L McNamaraPhysics Division, Department of Radiation Oncology, Massachusetts General Hospital and Harvard Medical School, Massachusetts.
Samuel P IngramDivision of Cancer Sciences, University of Manchester, Manchester, United Kingdom.
Michael J MerchantDivision of Cancer Sciences, University of Manchester, Manchester, United Kingdom.
Karen J KirkbyDivision of Cancer Sciences, University of Manchester, Manchester, United Kingdom.
Jan SchuemannPhysics Division, Department of Radiation Oncology, Massachusetts General Hospital and Harvard Medical School, Massachusetts.
Harald PaganettiPhysics Division, Department of Radiation Oncology, Massachusetts General Hospital and Harvard Medical School, Massachusetts.
Kevin M PrisePatrick G Johnston Centre for Cancer Research, Queen's University Belfast, Belfast, United Kingdom.
Stephen J McMahonPatrick G Johnston Centre for Cancer Research, Queen's University Belfast, Belfast, United Kingdom.
Harvard University · USQueen's University Belfast · GBThe Christie NHS Foundation Trust · GBCancer Research UK Manchester Institute · GBManchester Academic Health Science Centre · GBMassachusetts General Hospital · USUniversity of Manchester · GB

Funding

MDACC Clinical and Research Physics SupportU19CA021239 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI YEAP, BEOW Y · 2014 to 2018
$11.2M
TOPAS - nBio, a Monte Carlo tool for radiation biology researchR01CA187003 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI SCHUEMANN, JAN PATRICK OSCAR · 2015 to 2024
$4.8M
Cancer Research UK 28701NCI NIH HHS R01 CA187003NCI NIH HHS U19 CA021239
6 · The paper itself

Abstract

The induction and repair of DNA double-strand breaks (DSBs) are critical factors in the treatment of cancer by radiotherapy. To investigate the relationship between incident radiation and cell death through DSB induction many in silico models have been developed. These models produce and use custom formats of data, specific to the investigative aims of the researchers, and often focus on particular pairings of damage and repair models. In this work we use a standard format for reporting DNA damage to evaluate combinations of different, independently developed, models. We demonstrate the capacity of such inter-comparison to determine the sensitivity of models to both known and implicit assumptions. Specifically, we report on the impact of differences in assumptions regarding patterns of DNA damage induction on predicted initial DSB yield, and the subsequent effects this has on derived DNA repair models. The observed differences highlight the importance of considering initial DNA damage on the scale of nanometres rather than micrometres. We show that the differences in DNA damage models result in subsequent repair models assuming significantly different rates of random DSB end diffusion to compensate. This in turn leads to disagreement on the mechanisms responsible for different biological endpoints, particularly when different damage and repair models are combined, demonstrating the importance of inter-model comparisons to explore underlying model assumptions.

Indexed as

DNA RepairNeoplasmsComputer SimulationDNA Breaks, Double-StrandedDNA DamageHumans

Identifiers

PMID38014593
PMCPMC11590750
OpenAlexW4389098458

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.