Number and dynamics of micronuclei and near-tetraploidy predict prognosis in childhood acute leukaemia.

buccal micronuclei (Mn) children leukaemia predictors

Journal

Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia
ISSN: 1804-7521
Titre abrégé: Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub
Pays: Czech Republic
ID NLM: 101140142

Informations de publication

Date de publication:
22 Nov 2023
Historique:
medline: 24 11 2023
pubmed: 24 11 2023
entrez: 24 11 2023
Statut: aheadofprint

Résumé

This study aims to identify factors possibly contributing to complications in children with acute leukaemia. Despite diverse etiological causes, similar processes trigger the process of cell malignancy. Genomic instability has received considerable attention in this context. We conducted chromosomal analysis of bone marrow cells and measured the micronuclei (Mn) level in buccal cells over time. Statistical reliability assessment was performed using Analysis of variance (ANOVA), and the data were analyzed and visualized using the SPSS 12 statistical analysis software package. On the 15th day of treatment, our findings confirmed a statistically significant correlation (χ While it is commonly believed that a hyperdiploid clone with >50 chromosomes in childhood acute lymphoblastic leukaemia confers favorable outcome, our study revealed partially heterogeneous results and poor prognosis in patients with a near-tetraploid clone. We have also identified a correlation between the Mn level on the 33rd day of treatment and the development of complications. It is possible that the increased Mn values and the occurrence of relapses were influenced by the individual patient's sensitivity to the genotoxic effect of the medication.

Identifiants

pubmed: 37997902
doi: 10.5507/bp.2023.046
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Déclaration de conflit d'intérêts

The authors report no conflicts of interest in this work.

Auteurs

Sopiko Jashiashvili (S)

Tbilisi State Medical University, Tbilisi, Georgia.

Alla Zedginidze (A)

Ivane Beritashvili Center of Experimental Biomedicine, Tbilisi, Georgia.

Giorgi Ormotsadze (G)

Ivane Beritashvili Center of Experimental Biomedicine, Tbilisi, Georgia.

Asmat Shengelaia (A)

Tbilisi State Medical University, Tbilisi, Georgia.

Classifications MeSH