Abstract
N-Glycosylases excise the damaged adducts from DNA. 7,8-Dihydro-8- oxoguanine in human cells is repaired by OGG1 and hNTH1. The activities of hOGG1 and hNTH1 were measured, using modified and 32P labelled oligonucleotides, in bronchial biopsy samples of smoking patients with non-small cell lung carcinoma. The activity of hOOG1 was significantly higher in biopsies from tumour tissues compared with intra-individual control samples. On the contrary, the activity of endonuclease III homologue, hNTH1, was lower in tumours compared to controls. These opposing alterations in DNA repair enzymes may affect cancer growth due to the increased formation of AP sites.
Original language | English |
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Pages (from-to) | 191-195 |
Number of pages | 5 |
Journal | Cancer Letters |
Volume | 219 |
Issue number | 2 |
DOIs | |
Publication status | Published - Mar 10 2005 |
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Keywords
- Base excision repair
- DNA repair
- Formamidopyrimidine- DNA
- hNTH1
- Lung cancer
- Mutation
- OGG1
- Smoking
ASJC Scopus subject areas
- Cancer Research
- Molecular Biology
- Oncology
Cite this
Lung cancer in smoking patients inversely alters the activity of hOGG1 and hNTH1. / Radák, Z.; Goto, S.; Nakamoto, Hideko; Udud, Katalin; Papai, Zsolt; Horváth, I.
In: Cancer Letters, Vol. 219, No. 2, 10.03.2005, p. 191-195.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Lung cancer in smoking patients inversely alters the activity of hOGG1 and hNTH1
AU - Radák, Z.
AU - Goto, S.
AU - Nakamoto, Hideko
AU - Udud, Katalin
AU - Papai, Zsolt
AU - Horváth, I.
PY - 2005/3/10
Y1 - 2005/3/10
N2 - N-Glycosylases excise the damaged adducts from DNA. 7,8-Dihydro-8- oxoguanine in human cells is repaired by OGG1 and hNTH1. The activities of hOGG1 and hNTH1 were measured, using modified and 32P labelled oligonucleotides, in bronchial biopsy samples of smoking patients with non-small cell lung carcinoma. The activity of hOOG1 was significantly higher in biopsies from tumour tissues compared with intra-individual control samples. On the contrary, the activity of endonuclease III homologue, hNTH1, was lower in tumours compared to controls. These opposing alterations in DNA repair enzymes may affect cancer growth due to the increased formation of AP sites.
AB - N-Glycosylases excise the damaged adducts from DNA. 7,8-Dihydro-8- oxoguanine in human cells is repaired by OGG1 and hNTH1. The activities of hOGG1 and hNTH1 were measured, using modified and 32P labelled oligonucleotides, in bronchial biopsy samples of smoking patients with non-small cell lung carcinoma. The activity of hOOG1 was significantly higher in biopsies from tumour tissues compared with intra-individual control samples. On the contrary, the activity of endonuclease III homologue, hNTH1, was lower in tumours compared to controls. These opposing alterations in DNA repair enzymes may affect cancer growth due to the increased formation of AP sites.
KW - Base excision repair
KW - DNA repair
KW - Formamidopyrimidine- DNA
KW - hNTH1
KW - Lung cancer
KW - Mutation
KW - OGG1
KW - Smoking
UR - http://www.scopus.com/inward/record.url?scp=13944270220&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=13944270220&partnerID=8YFLogxK
U2 - 10.1016/j.canlet.2004.07.008
DO - 10.1016/j.canlet.2004.07.008
M3 - Article
C2 - 15723719
AN - SCOPUS:13944270220
VL - 219
SP - 191
EP - 195
JO - Cancer Letters
JF - Cancer Letters
SN - 0304-3835
IS - 2
ER -