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


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
09 Dec 2022
Historique:
received: 04 05 2022
accepted: 28 11 2022
entrez: 9 12 2022
pubmed: 10 12 2022
medline: 15 12 2022
Statut: epublish

Résumé

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.

Identifiants

pubmed: 36494413
doi: 10.1038/s41598-022-25328-6
pii: 10.1038/s41598-022-25328-6
pmc: PMC9734114
doi:

Substances chimiques

X-ray Repair Cross Complementing Protein 1 0
TGFB1 protein, human 0
Transforming Growth Factor beta1 0
XRCC1 protein, human 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

21306

Informations de copyright

© 2022. The Author(s).

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Auteurs

Emina Mališić (E)

Department of Experimental Oncology, Institute for Oncology and Radiology of Serbia, Pasterova 14, 11 000, Belgrade, Serbia. eminamalisic@yahoo.co.uk.

Nina Petrović (N)

Department of Experimental Oncology, Institute for Oncology and Radiology of Serbia, Pasterova 14, 11 000, Belgrade, Serbia.
"VINČA" Institute of Nuclear Sciences-National Institute of the Republic of Serbia, University of Belgrade, Belgrade, Serbia.

Muriel Brengues (M)

IRCM, INSERM, University Montpellier, ICM, Montpellier, France.

David Azria (D)

IRCM, INSERM, University Montpellier, ICM, Montpellier, France.

Ivana Z Matić (IZ)

Department of Experimental Oncology, Institute for Oncology and Radiology of Serbia, Pasterova 14, 11 000, Belgrade, Serbia.

Ivana Srbljak Ćuk (I)

Department of Experimental Oncology, Institute for Oncology and Radiology of Serbia, Pasterova 14, 11 000, Belgrade, Serbia.

Katarina Kopčalić (K)

Department of Radiation Oncology, Institute for Oncology and Radiology of Serbia, Belgrade, Serbia.

Tatjana Stanojković (T)

Department of Experimental Oncology, Institute for Oncology and Radiology of Serbia, Pasterova 14, 11 000, Belgrade, Serbia.

Marina Nikitović (M)

Department of Radiation Oncology, Institute for Oncology and Radiology of Serbia, Belgrade, Serbia.
Faculty of Medicine, University of Belgrade, Belgrade, Serbia.

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Classifications MeSH