Evidence map›Paper›PMID 39820036›Full record

ArticleScientific reports2025

Mapping neutron biological effectiveness for DNA damage induction as a function of incident energy and depth in a human sized phantom.

Alice Mentana, Virgilio Quaresima, Pavel Kundrát, Isabella Guardamagna, Leonardo Lonati, Ombretta Iaria, Andrea Previtali, Giorgia Santi Amantini, Luca Lunati, Virginia Boretti and 5 more

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

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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

15 authors.

Alice MentanaRadiation Biophysics and Radiobiology Laboratory, Physics Department, University of Pavia, Pavia, Italy.
Virgilio QuaresimaRadiation Biophysics and Radiobiology Laboratory, Physics Department, University of Pavia, Pavia, Italy.
Pavel KundrátDepartment of Radiation Dosimetry, Nuclear Physics Institute, Czech Academy of Sciences, Prague, Czechia.
Isabella GuardamagnaRadiation Biophysics and Radiobiology Laboratory, Physics Department, University of Pavia, Pavia, Italy.
Leonardo LonatiRadiation Biophysics and Radiobiology Laboratory, Physics Department, University of Pavia, Pavia, Italy.
Ombretta IariaRadiation Biophysics and Radiobiology Laboratory, Physics Department, University of Pavia, Pavia, Italy.
Andrea PrevitaliRadiation Biophysics and Radiobiology Laboratory, Physics Department, University of Pavia, Pavia, Italy.
Giorgia Santi AmantiniPhysics Department, University of Roma Tor Vergata, Rome, Italy.
Luca LunatiPhysics Department, University of Roma Tor Vergata, Rome, Italy.
Virginia BorettiPhysics Department, University of Roma Tor Vergata, Rome, Italy.
Livio NariciPhysics Department, University of Roma Tor Vergata, Rome, Italy.
Luca Di FinoASI, Italian Space Agency, Rome, Italy.
Luca BocchiniThales Alenia Space-Italy, Turin, Italy.
Claudio CiprianiThales Alenia Space-Italy, Turin, Italy.
Giorgio BaioccoRadiation Biophysics and Radiobiology Laboratory, Physics Department, University of Pavia, Pavia, Italy. giorgio.baiocco@unipv.it.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We present new developments for an ab-initio model of the neutron relative biological effectiveness (RBE) in inducing specific classes of DNA damage. RBE is evaluated as a function of the incident neutron energy and of the depth inside a human-sized reference spherical phantom. The adopted mechanistic approach traces neutron RBE back to its origin, i.e. neutron physical interactions with biological tissues. To this aim, we combined the simulation of radiation transport through biological matter, performed with the Monte Carlo code PHITS, and the prediction of DNA damage using analytical formulas, which ground on a large database of biophysical radiation track structure simulations performed with the code PARTRAC. In particular, two classes of DNA damage were considered: sites and clusters of double-strand breaks (DSBs), which are known to be correlated with cell fate following radiation exposure. Within a coherent modelling framework, this approach tackles the variation of neutron RBE in a wide energy range, from thermal neutrons to neutrons of hundreds of GeV, and reproduces effects related to depth in the human-sized receptor, as well as to the receptor size itself. Besides providing a better mechanistic understanding of neutron biological effectiveness, the new model can support better-informed decisions for radiation protection: indeed, current neutron weighting (ICRP)/quality (U.S. NRC) factors might be insufficient for use in some radiation protection applications, because they do not account for depth. RBE predictions obtained with the reported model were successfully compared to the currently adopted radiation protection standards when the depth information is not relevant (at the shallowest depth in the phantom or for very high energy neutrons). However, our results demonstrate that great care is needed when applying weighting factors as a function of incident neutron energy only, not explicitly considering RBE variation in the target. Finally, to facilitate the use of our results, we propose look-up RBE tables, explicitly considering the depth variable, and an analytical representation of the maximal RBE vs. neutron energy.

Indexed as

DNA DamageNeutronsPhantoms, ImagingRelative Biological EffectivenessDNA Breaks, Double-StrandedHumansMonte Carlo Method

Identifiers

PMID39820036
PMCPMC11739508

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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.