Abstract | OBJECTIVE: METHODS: Using the P1 enriched version of 32P-postlabeling for hydrophobic DNA adducts detection on polyethyleneimine (PEI) cellulose thin layer chromatograms (TLC) we examined 11 uterine cancer DNAs. The quantification of the adducts was performed by Cerenkov counting of the spots. ER and PR status was recognized histochemically and H-score estimate was performed for each investigated cancer tissue. Patterns of uterine cancer DNA adducts were compared to the maps of adducts recognized in normal human endometrium. RESULTS: In three of the studied uterine cancers there was no positive staining of ER and PR; in one case there was a weak ER staining but PR staining was negative. In ER negative tumors the A level was significantly higher than in ER positive cancers (138.1 +/- 64.1 vs. 49.7 +/- 26.8 adducts per 10(9) nucleotides, respectively, p < 0.05). Highest A levels were found in two ER and PR negative G3 metastatic tumors. Finally, in all investigated cancers there was a strong, inverse correlation between ER content and A level (r = -0.67, p < 0.03). In addition, the correlation between PR level and A was of borderline significance (r = -0.6, p = 0.053). The TLC patterns of adducts in uterine tumors were found to be qualitatively similar, but not quantitatively, to those observed in normal human endometrium DNA. CONCLUSION:
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Authors | K Postawski, E Olech-Fudali, E Korobowicz, J A Jakowicki, G Keith, W Baranowski |
Journal | Ginekologia polska
(Ginekol Pol)
Vol. 72
Issue 9
Pg. 709-16
(Sep 2001)
ISSN: 0017-0011 [Print] Poland |
Vernacular Title | Hydrofobowe addukty DNA w relacji do gestości receptorów estrogenowych i progesteronowego w gruczolakorakach błony śluzowej macicy u kobiet. |
PMID | 11757482
(Publication Type: English Abstract, Journal Article)
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Chemical References |
- DNA Adducts
- DNA, Neoplasm
- Receptors, Estrogen
- Receptors, Progesterone
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Topics |
- Autoradiography
- DNA Adducts
(analysis)
- DNA, Neoplasm
(analysis)
- Female
- Humans
- Receptors, Estrogen
(analysis)
- Receptors, Progesterone
(analysis)
- Uterine Neoplasms
(genetics, pathology)
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