Abstract |
Human DNA polymerases kappa, eta, iota, and zeta are responsible for the translesion DNA synthesis. Numerous in vitro studies indicated that these enzymes may contribute to DNA lesion-triggered and spontaneous mutation. We measured the transcripts of these 4 enzymes in 131 self-paired cancerous and non- tumor samples, including 23 lung cancers, 49 stomach cancers, and 59 colorectal cancers. Our results indicated that, except pol eta in colorectal cancers, these enzymes are all significantly down-regulated in human lung, stomach, and colorectal cancers, suggesting that these enzymes are probably not closely associated with the elevated mutations in human cancer.
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Authors | Qiangrong Pan, Yongming Fang, Yang Xu, Kun Zhang, Xun Hu |
Journal | Cancer letters
(Cancer Lett)
Vol. 217
Issue 2
Pg. 139-47
(Jan 20 2005)
ISSN: 0304-3835 [Print] Ireland |
PMID | 15617831
(Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- DNA-Directed DNA Polymerase
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Topics |
- Colorectal Neoplasms
(enzymology)
- DNA-Directed DNA Polymerase
(metabolism)
- Down-Regulation
- Female
- Humans
- Lung Neoplasms
(enzymology)
- Male
- Reverse Transcriptase Polymerase Chain Reaction
- Stomach Neoplasms
(enzymology)
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