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Comparative analysis of thymidylate synthase, thymidine phosphorylase and dihydropyrimidine dehydrogenase expression in colorectal cancer and surrounding normal tissue
M Zimovjanova, V Sykora, J Novotny, J Gatek, L Petruzelka, L Holubec, L Pecen
Language English Country Slovakia
Grant support
ND7575
MZ0
CEP Register
Digital library NLK
Full text - Část
Source
- MeSH
- Dihydrouracil Dehydrogenase (NADP) genetics metabolism MeSH
- Gene Expression MeSH
- Financing, Organized MeSH
- Colorectal Neoplasms enzymology MeSH
- Humans MeSH
- RNA, Messenger analysis metabolism MeSH
- Polymerase Chain Reaction MeSH
- Intestinal Mucosa enzymology MeSH
- Thymidine Phosphorylase genetics metabolism MeSH
- Thymidylate Synthase genetics metabolism MeSH
- Check Tag
- Humans MeSH
Thymidylate synthase [TS], thymidine phosphorylase [TP] and dihydropyrimidine dehydrogenase [DPD] play the essential role in the activation and catabolism of the fluoropyrimidines used in cancer therapy. Its expression may influence the antitumor activity or toxicity of these drugs. We studied the expression levels of selected enzymes in colorectal tumors and adjacent normal mucosa. The analysis of TS, TP and DPD gene expression was performed using quantitative Real time PCR technique (Roche) in 15 (TS), 64 (TP) and 12 (DPD) of 64 colorectal cancer patients. The mean gene expression of TS, TP and DPD was found to be 3.29; 3.79 and 8.24 in tumors and 1.88; 3.80 and 19.69 in normal mucosa. The corresponding median gene expression was 1.87; 2.32 and 4.50 for tumors and 2.14; 2.63 and 11.64 for normal tissue. We did not find any significant differences in TS, TP and DPD gene expression between colorectal tumor and surrounding mucosa.
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- $a Department of Oncology, General Teaching Hospital, 12880 Prague, Czech Republic onkologie@seznam.cz
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- $a Thymidylate synthase [TS], thymidine phosphorylase [TP] and dihydropyrimidine dehydrogenase [DPD] play the essential role in the activation and catabolism of the fluoropyrimidines used in cancer therapy. Its expression may influence the antitumor activity or toxicity of these drugs. We studied the expression levels of selected enzymes in colorectal tumors and adjacent normal mucosa. The analysis of TS, TP and DPD gene expression was performed using quantitative Real time PCR technique (Roche) in 15 (TS), 64 (TP) and 12 (DPD) of 64 colorectal cancer patients. The mean gene expression of TS, TP and DPD was found to be 3.29; 3.79 and 8.24 in tumors and 1.88; 3.80 and 19.69 in normal mucosa. The corresponding median gene expression was 1.87; 2.32 and 4.50 for tumors and 2.14; 2.63 and 11.64 for normal tissue. We did not find any significant differences in TS, TP and DPD gene expression between colorectal tumor and surrounding mucosa.
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