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The Application of Qualitative Analysis of DNA Bulky Adducts in the Diagnoosis of Brain Tumours

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Damage to DNA(base modification) is generally considered to be causative and directly related to tumour formation. Interaction of chemical carcinogens with DNA either directly or after metabolic activation, typically involves covalent binding of an electrophilic compound with a nucleophilic site in DNA. Guanine is by far the most prevalent target although adducts have been reported for all bases. We analysed the occurrence of bulky hydrophobic derivatives of DNA (adducts) in human brain tumour tissues. DNA was isolated, enzymatically digested to nucleotides and labeled with [_-32P]ATP and T4 polynucleotide kinase. Radioactive nucleotides were separated on anion-exchange polyethyleneimine cellulose (PEI) thin layer chromatography (TLC).We found that all brain tumours have similar DNA adducts pattern, although there are some significant differences for a particular disease. It turned out that DNA of a glioblastoma multiforme contains a rich array of modified bases in contrast to meningeoma tissues DNA, which shows only a few nucleotides. Location of spots on TLC of DNA adducts resemble a triangle, which is specific for brain tumours. This method of analysis may be very useful in classification and clinical diagnosis of brain tumours.
Rocznik
Strony
1607--1614
Opis fizyczny
Bibliogr. 16 poz., rys.
Twórcy
  • Department of Neurosurgery, Karol Marcinkowski University School of Medical Sciences, Przybyszewskiego 49, 60-355 Poznań, Poland
  • Faculty of Chemistry, A. Mickiewicz University, Grunwaldzka 6, 60-780 Poznań, Poland
  • Institute of Bioorganic Chemistry of the Polish Academy of Sciences, Noskowskiego 12, 61-704 Poznań, Poland
autor
  • Department of Neurosurgery, Karol Marcinkowski University School of Medical Sciences, Przybyszewskiego 49, 60-355 Poznań, Poland
autor
  • Department of Neurosurgery, Karol Marcinkowski University School of Medical Sciences, Przybyszewskiego 49, 60-355 Poznań, Poland
  • Institute of Bioorganic Chemistry of the Polish Academy of Sciences, Noskowskiego 12, 61-704 Poznań, Poland
Bibliografia
  • 1. Harris C.C., Carcinogenesis, 10, 1563 (1989).
  • 2. Perera F.P. and Weinstein I.B., Carcinogenesis, 21, 517 (2000).
  • 3. Rether B., Pohl-Leszkowicz A., Guillemaut P. and Keith G., FEBS Lett., 263, 172 (1990).
  • 4. Gupta R.C., Postlabelling Methods for Detection of DNA Adducts, Ed. D.H. Philips, M. Castegi H. Bartsch, Lyon, International Agency for Research on Cancer, pp. 11-23, 1993.
  • 5. Pohl-Leszkowicz A., Weber-Lotfi F., Masfaraud J.F., Devaux A., Laouedj A., Guillemaut P., Mai C., Rether B., Monod G. and Dirheimer G., Postlabelling Methods for Detection of DNA Adducts, Ed. D. H. Philips, M. Castegnaro & H. Bartsch, Lyon, International Agency for Research on Cancer, pp. 373-378, 1993.
  • 6. Asan E., Fasshauer I., Wild D. and Henschler D., Carcinogenesis, 8, 1589 (1987).
  • 7. Roy A.K., El-Bayoumy K. and Hecht S.S., Carcinogenesis, 10,195 (1989).
  • 8. Randerath K., Reddy M.V. and Gupta R.C., Proc. Natl. Acad. Sci. USA, 87, 6126 (1981).
  • 9. Miller S.A., Dykes D.D. and Polesky H.F., Nucleic Acids Res., 16, 1215 (1988).
  • 10. Reddy M.V. and Randerath K., Carcinogenesis, 7, 1543 (1986).
  • 11. Pollack M.N. and Foulkes W.D., Nature Reviews Cancer, 3, 297 (2003).
  • 12. Phillips D.H., Carcinogenesis, 23, 1979 (2002).
  • 13. Jensen K.G., Onfelt A., Poulsen H.E., Doehmer J. and Loft S., Carcinogenesis, 14, 2115 (199
  • 14. Randerath K., Randerath E., Danna T.F., van Golen K.L. and Putman K.L., Carcinogenesis, 10, (1989).
  • 15. Reddy M. V., Gupta R.C., Randerath E. and Randerath K., Carcinogenesis, 5, 231 (1984).
  • 16. Boysen G. and Hecht S.S., Mut. Res., 543, 17 (2003).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BUJ1-0022-0025
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