Evidence map›Paper›PMID 36494413›Full record

ArticleScientific reports2022

Association of polymorphisms in TGFB1, XRCC1, XRCC3 genes and CD8 T-lymphocyte apoptosis with adverse effect of radiotherapy for prostate cancer.

Emina Mališić, Nina Petrović, Muriel Brengues, David Azria, Ivana Z Matić, Ivana Srbljak Ćuk, Katarina Kopčalić, Tatjana Stanojković, Marina Nikitović

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.9field-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

12 citing papers in PubMed, 15 citations in OpenAlex.

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  2. Genotoxicity of cancer therapies and the risk of secondary malignancies: toward personalized prevention.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
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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

9 authors at 3 institutions in 2 countries.

Emina MališićDepartment of Experimental Oncology, Institute for Oncology and Radiology of Serbia, Pasterova 14, 11 000, Belgrade, Serbia. eminamalisic@yahoo.co.uk.ORCID http://orcid.org/0000-0001-5733-291X
Nina PetrovićDepartment of Experimental Oncology, Institute for Oncology and Radiology of Serbia, Pasterova 14, 11 000, Belgrade, Serbia.
Muriel BrenguesIRCM, INSERM, University Montpellier, ICM, Montpellier, France.
David AzriaIRCM, INSERM, University Montpellier, ICM, Montpellier, France.
Ivana Z MatićDepartment of Experimental Oncology, Institute for Oncology and Radiology of Serbia, Pasterova 14, 11 000, Belgrade, Serbia.
Ivana Srbljak ĆukDepartment of Experimental Oncology, Institute for Oncology and Radiology of Serbia, Pasterova 14, 11 000, Belgrade, Serbia.
Katarina KopčalićDepartment of Radiation Oncology, Institute for Oncology and Radiology of Serbia, Belgrade, Serbia.
Tatjana StanojkovićDepartment of Experimental Oncology, Institute for Oncology and Radiology of Serbia, Pasterova 14, 11 000, Belgrade, Serbia.
Marina NikitovićDepartment of Radiation Oncology, Institute for Oncology and Radiology of Serbia, Belgrade, Serbia.
Oncology Institute of Vojvodina · RSInserm · FRUniversity of Belgrade · RS

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The genetic background of each person might affect the severity of radiotherapy (RT)-induced normal tissue toxicity. The aim of study was to evaluate the influence of TGFB1 C-509T and Leu10Pro, XRCC1 Arg280His and XRCC3 Thr241Met polymorphisms as well as the level of radiation-induced CD8 T-lymphocyte apoptosis (RILA) on adverse effects of RT for prostate cancer (PCa). The study included 88 patients with localized or locally advanced PCa who were treated with RT. The polymorphisms were determined by PCR-RFLP analysis on DNA from peripheral blood mononuclear cells. RILA values were measured by flow cytometry. We found that CT genotype of TGFB1 C-509T could be protective biomarker for acute genitourinary (GU) and gastrointestinal (GI) radiotoxicity, while Thr variant of XRCC3 Thr241Met could predict the risk for acute GU radiotoxicity. Correlation between RILA values and toxicity was not detected. Univariate logistic regression analysis showed that Gleason score and risk group were risk factors for late GU, while for late GI radiotoxicity it was diabetes mellitus type 2. However, in multivariate model those were not proven to be significant and independent risk factors. Identification of assays combination predicting individual radiosensitivity is a crucial step towards personalized RT approach.

Indexed as

Prostatic NeoplasmsRadiation InjuriesApoptosisHumansLeukocytes, MononuclearMalePolymorphism, Single NucleotideT-LymphocytesTransforming Growth Factor beta1X-ray Repair Cross Complementing Protein 1TGFB1 protein, humanTransforming Growth Factor beta1X-ray Repair Cross Complementing Protein 1XRCC1 protein, human

Identifiers

PMID36494413
PMCPMC9734114
OpenAlexW4311664749

What OpenQuestion holds

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LicenceCC BY
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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.