Allelic loss on chromosomes 2q21 and 19p13.2 in oxyphilic thyroid tumors

Karmen Stankov, Alessandro Pastore, Luca Toschi, James McKay, Fabienne Lesueur, Jean Louis Kraimps, Dominique Bonneau, Hélène Gibelin, Pierre Levillain, Marco Volante, Mauro Papotti, Giovanni Romeo

Research output: Contribution to journalArticle

27 Citations (Scopus)

Abstract

Hürthle thyroid tumors are characterized by frequent numerical chromosomal aberrations, including aneuploidy or polyploidy, losses and gains of some chromosomal regions and DNA fragmentation. In recent years, great attention has been paid to the combined analysis of morphologic and genetic features of oxyphilic tumors and to the elucidation of their pathogenesis. We analyzed for loss of heterozygosity (LOH) of the candidate regions for TCO (thyroid tumor with cell oxyphilia) and NMTC1 (nonmedullary thyroid carcinoma 1), 2 loci already mapped on chromosomes 19p13.2 and 2q21, respectively. Matched normal and tumor DNA samples from 70 patients with sporadic oxyphilic thyroid tumors and 20 with sporadic follicular tumors were subjected to microsatellite analysis using 10 markers on 19p13.2 and 6 markers on 2q21. This approach led us to the observation of a more significant LOH in oxyphilic than in follicular tumors. Allelic loss in tumor samples was evenly distributed in both 19p13.2 and 2q21 regions, in accordance with the established linkage of TCO and NMTC1 for inherited tumors. In order to investigate the possible contribution of both susceptibility loci in oxyphilic tumors, the family that led to the original mapping of TCO locus was reanalyzed for the markers in the 2q21 region. This led to the exclusion of linkage with the NMTC1 locus and to the refutation of the digenic inheritance hypothesis at least in this family.

Original languageEnglish
Pages (from-to)463-467
Number of pages5
JournalInternational Journal of Cancer
Volume111
Issue number3
DOIs
Publication statusPublished - Sep 1 2004

Fingerprint

Loss of Heterozygosity
Thyroid Gland
Chromosomes
Neoplasms
Polyploidy
Aneuploidy
DNA Fragmentation
Chromosome Aberrations
Microsatellite Repeats
Observation

Keywords

  • 19p13.2
  • 2q21
  • Loss of heterozygosity
  • Microsatellite analysis
  • Oxyphilic thyroid tumors

ASJC Scopus subject areas

  • Cancer Research
  • Oncology

Cite this

Stankov, K., Pastore, A., Toschi, L., McKay, J., Lesueur, F., Kraimps, J. L., ... Romeo, G. (2004). Allelic loss on chromosomes 2q21 and 19p13.2 in oxyphilic thyroid tumors. International Journal of Cancer, 111(3), 463-467. https://doi.org/10.1002/ijc.20259

Allelic loss on chromosomes 2q21 and 19p13.2 in oxyphilic thyroid tumors. / Stankov, Karmen; Pastore, Alessandro; Toschi, Luca; McKay, James; Lesueur, Fabienne; Kraimps, Jean Louis; Bonneau, Dominique; Gibelin, Hélène; Levillain, Pierre; Volante, Marco; Papotti, Mauro; Romeo, Giovanni.

In: International Journal of Cancer, Vol. 111, No. 3, 01.09.2004, p. 463-467.

Research output: Contribution to journalArticle

Stankov, K, Pastore, A, Toschi, L, McKay, J, Lesueur, F, Kraimps, JL, Bonneau, D, Gibelin, H, Levillain, P, Volante, M, Papotti, M & Romeo, G 2004, 'Allelic loss on chromosomes 2q21 and 19p13.2 in oxyphilic thyroid tumors', International Journal of Cancer, vol. 111, no. 3, pp. 463-467. https://doi.org/10.1002/ijc.20259
Stankov, Karmen ; Pastore, Alessandro ; Toschi, Luca ; McKay, James ; Lesueur, Fabienne ; Kraimps, Jean Louis ; Bonneau, Dominique ; Gibelin, Hélène ; Levillain, Pierre ; Volante, Marco ; Papotti, Mauro ; Romeo, Giovanni. / Allelic loss on chromosomes 2q21 and 19p13.2 in oxyphilic thyroid tumors. In: International Journal of Cancer. 2004 ; Vol. 111, No. 3. pp. 463-467.
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AU - Kraimps, Jean Louis

AU - Bonneau, Dominique

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