Quercetin induces structural chromosomal aberrations and uncommon rearrangements in bovine cells transformed by the E7 protein of bovine papillomavirus type 4

Bovine papillomavirus type 4 (BPV‐4) and bracken fern are cofactors in the carcinogenesis of the upper gastrointestinal (GI) tract of cattle. An experimental in vitro model system has been developed to analyse the co‐operation between the viral transforming protein E7, the cellular ras oncogene and...

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Veröffentlicht in:Veterinary & comparative oncology 2003-03, Vol.1 (1), p.15-21
Hauptverfasser: Leal, A. M., Ferraz, O. P., Carvalho, C., Freitas, A. C., Beniston, R. G., Beçak, W., Campo, M. S., Stocco dos Santos, R. C.
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Sprache:eng
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Zusammenfassung:Bovine papillomavirus type 4 (BPV‐4) and bracken fern are cofactors in the carcinogenesis of the upper gastrointestinal (GI) tract of cattle. An experimental in vitro model system has been developed to analyse the co‐operation between the viral transforming protein E7, the cellular ras oncogene and quercetin, one of the mutagens of bracken fern, during neoplastic progression of primary bovine cells. We now report cytogenetic studies of these cells at different stages of malignant transformation: parental primary non‐transformed PalF cells; E7R cells transformed by BPV‐4 E7 and activated ras but not tumorigenic, and tumorigenic E7Q cells derived from E7R cells after treatment with quercetin. All cell lines presented increased numbers of aneuploid cells. The rate of structural chromosomal aberrations observed was increased in transformed cells. In addition, E7Q cells showed chromosomes with peculiar rearrangements, which resulted in metacentric and submetacentric marker chromosomes, with an increase in the mean chromosome arm number. These markers were the products of possible centric fusions. These aberrations and rearrangements were distributed throughout the karyotype, no specific chromosome was involved and the heterochromatic centromeric regions appeared to be preserved.
ISSN:1476-5810
1476-5829
DOI:10.1046/j.1476-5829.2003.00008.x