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Dive into the research topics where Gábor Székely is active.

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Featured researches published by Gábor Székely.


Mutagenesis | 2016

Relationship between spontaneous frequency of aneuploidy and cancer risk in 2145 healthy Hungarian subjects

Gyöngyi Farkas; Zsolt Jurányi; Gábor Székely; Zsuzsa S. Kocsis; Sarolta Gundy

Numerical and structural chromosomal abnormalities are the hallmarks of cancer. Whereas the structural chromosome aberrations got more substantial attention for cancer risk assessment in a healthy population, the role of aneuploidy is much less understood in this respect. We analysed the frequency of numerical (and structural) aberrations in peripheral blood lymphocytes of 2145 healthy individuals between 1989 and 2010, taking into account different biological- and exposure-conditions. We also studied to what extent chromosome gains or losses may predict the probability of cancer. The average frequency of all aneuploid cells was 1.78±0.06% in the entire study population, which increased linearly with age. Gender and smoking did not influence the values, however, occupational exposures did. The highest frequency of aneuploidy was found in chemical industry-workers (1.89±0.05%) compared with the lowest value of medical radiation workers (1.44±0.10%), respectively. No correlation was found between numerical and structural chromosomal aberrations. Cancer incidence followed for 1-23 years after the chromosome analysis showed a 1.26-fold relative risk (confidence interval: 1.02-1.58; P = 0.04) for those with higher frequency of aneuploid cells (1.82% vs. 1.44% in controls). Hypodiploidy had higher impact on the cancer risk than hyperdiploidy (1.72% vs. 0.10%). Our findings on the frequency of numerical aberrations in a healthy cohort represent the largest cytogenetic database from one laboratory with an unchanged mechanistic scoring method during a 30-year period, and provide basic information not only for genotoxicological studies but also confirm the association between numerical aberrations and cancer risk.


Cancer Reports | 2018

Progressive breast fibrosis caused by extreme radiosensitivity: Oncocytogenetic diagnosis and treatment by reconstructive flap surgery

Norbert Mészáros; Gyöngyi Farkas; Gábor Székely; Zsuzsa S. Kocsis; Péter Kelemen; János Fodor; Csaba Polgár; Zsolt Jurányi

Fibrosis, a proliferative response of fibrocytes after tissue injury, is a common sequela of external radiotherapy and can vary greatly among patients even in the absence of DNA repair syndromes, due to their different intrinsic radiosensitivity. Fibrosis is also a serious cosmetic problem for patients, and in some cases it can also imply pain.


Carcinogenesis | 2002

Genetic polymorphisms of DNA repair and xenobiotic-metabolizing enzymes: role in mutagen sensitivity

Jarno Tuimala; Gábor Székely; Sarolta Gundy; Ari Hirvonen; Hannu Norppa


Mutation Research | 2004

Genetic polymorphisms of DNA repair and xenobiotic-metabolizing enzymes: effects on levels of sister chromatid exchanges and chromosomal aberrations.

Jarno Tuimala; Gábor Székely; Harriet Wikman; Hilkka Järventaus; Ari Hirvonen; Sarolta Gundy; Hannu Norppa


Mutagenesis | 2003

Does the bleomycin sensitivity assay express cancer phenotype

Gábor Székely; Éva Remenár; Miklós Kásler; Sarolta Gundy


Mutagenesis | 2005

Mutagen sensitivity of patients with cancer at different sites of the head and neck

Gábor Székely; Éva Remenár; Miklós Kásler; Sarolta Gundy


Magyar onkologia | 2001

[Exposure or cancer predisposition? Cytogenetic examination of head and neck squamous cancer patients]

Gábor Székely; Éva Remenár; Miklós Kásler; Sarolta Gundy


Magyar onkologia | 2015

Frequency of spontaneous aneuploidy in the healthy Hungarian population

Gyöngyi Farkas; Gábor Székely; Nagyezsda Vass; Krisztina Kiss; Sarolta Gundy


Magyar onkologia | 2008

Problems occurring in the application of cytogenetic biomarkers for alcoholics with and without malignant diseases

Sarolta Gundy; Gábor Székely; Gyöngyi Farkas; Attila Pulay; Éva Remenár


Mutation Research | 2005

Corrigendum to “Genetic polymorphisms of DNA repair and xenobiotic-metabolizing enzymes: effects on levels of sister chromatid exchanges and chromosomal aberrations” [Mutat. Res. 554 (2004) 319–333]

Jarno Tuimala; Gábor Székely; Harriet Wikman; Hilkka Järventaus; Ari Hirvonen; Sarolta Gundy; Hannu Norppa

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