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Poster session 04

1436P - Genotoxic effect of bullying in children and adolescents with and without central nervous system cancer

Date

10 Sep 2022

Session

Poster session 04

Topics

Patient Education and Advocacy;  Clinical Research;  Cancer in Adolescents and Young Adults (AYA);  Primary Prevention;  Genetic and Genomic Testing

Tumour Site

Presenters

Celia Beatriz Gonzalez-Alcorta

Citation

Annals of Oncology (2022) 33 (suppl_7): S653-S659. 10.1016/annonc/annonc1071

Authors

C.B. Gonzalez-Alcorta1, C.H. Burciaga-Flores1, F. Alcorta-Nuñez1, M..D.R. Velazco-Campos2, L. Rojas-Patlán2, D.C. Pérez-Ibave1, J.F. Gonzalez Guerrero1, O. Vidal-Gutiérrez1, L.E. Martínez-De Villarreal2, A. Alcorta-Garza1

Author affiliations

  • 1 Medical Oncology Department, Hospital Universitario Dr José Eleuterio Gonzalez, 64460 - Monterrey/MX
  • 2 Genetics Department, Hospital Universitario Dr José Eleuterio Gonzalez, 64460 - Monterrey/MX

Resources

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Abstract 1436P

Background

Micronuclei analysis is considered in oncology as a potential biomarker, used for risk assessment and prognosis purposes. This pilot study aimed to determine if there is a genotoxic effect caused by bullying in children and adolescents, through the examination of the difference between the frequency of bullying, micronuclei, and other nuclear abnormalities, between Central Nervous System cancer patients and healthy volunteers.

Methods

Prior Ethics Committee approval. Subjects from 4-17 y/o were recruited (N=39): 19 patients with CNS cancer in treatment and 20 healthy volunteers. All participants answered questionnaires: PedsQL 4.0, family violence and bullying. Samples were collected by exfoliating buccal mucosa through cytobrush. Participants were divided in four groups according to diagnosis and experience of bullying.

Results

No age or sex difference was observed between groups; the most frequent tumor was astrocytoma. 23 subjects (59%) met the criteria for bullying. Correlating sex and bullying, 12 (66%) were males of which 6 (50%) were patients and 6 (50%) volunteers, and 11 (52.3%) were females, 5 (45.4%) patients and 6 (54.5%) volunteers, with no statistic difference. Significant differences in micronuclei were found among groups (Table). Table: 1436P

Distribution of nuclear abnormalities

Nuclear abnormalities p <0.05* Group A Patients w/o bullying N=8 Group B Healthy w/o bullying N=8 Group C Healthy w/ bullying N=12 Group D* Patients w/ bullying N=11
M SD M SD M SD M SD
Binucleated 1.38 1.50 1.63 1.84 2.83 2.72 4.64 3.35
B. eggs 5.88 4.82 2.63 2.97 3.58 4.29 7.09 7.07
Karyolysis* 24.63 18.15 17.63 17.99 9.17 15.47 25.18 17.67
Karyorrhexis* 18.75 15.34 7.88 8.42 5.92 5.55 20.45 12.37
MNs* 14.75 3.99 5.50 4.42 9.0 12.82 12.18 6.85
NBUDs* 0.88 1.12 0.38 0.51 1.17 1.33 3.91 4.23
Pyknosis* 12.75 8.06 9.50 8.66 5.0 7.67 13.64 9.88
Total* 79.0 34.79 45.13 38.68 36.67 34.02 87.07 44.48

Conclusions

Correlation between binucleated cells, NBUDs and bullying suggest the genotoxic effect of the latter. Findings open a new investigation line, to generate more information between abuse and genetic damage and enforce preventing strategies for both mental and physical health on childhood and adolescence.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

Unviersidad Autonoma de Nuevo León.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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