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Article: The modulating role of nuclear factor-κB in the action of α7-nicotinic acetylcholine receptor and cross-talk between 5-lipoxygenase and cyclooxygenase-2 in colon cancer growth induced by 4-(N-methyl-N- nitrosamino)-1-(3-pyridyl)-1-butanone

TitleThe modulating role of nuclear factor-κB in the action of α7-nicotinic acetylcholine receptor and cross-talk between 5-lipoxygenase and cyclooxygenase-2 in colon cancer growth induced by 4-(N-methyl-N- nitrosamino)-1-(3-pyridyl)-1-butanone
Authors
Issue Date2004
Citation
Journal of Pharmacology and Experimental Therapeutics, 2004, v. 311, n. 1, p. 123-130 How to Cite?
Abstract4-(N-Methyl-N-nitrosamino)-1-(3-pyridyl)-1-butanone (NNK), the tobacco-specific nitrosamine, induces lung cancer in all animal species tested and is thought to contribute significantly to the high lung cancer burden associated with smoking. However, there is no report whether NNK could promote colon cancer growth. To address this hypothesis and the possible signaling pathways involved, we used SW1116 colon cancer cell line to study these biological events in vitro. Results showed that NNK, after 5-h treatment, stimulated cell proliferation, enhanced α7-nicotinic acetylcholine receptor (α7-nAChR) mRNA levels and nuclear factor-κB (NF-κB) DNA binding activity, as well as 5-lipoxygenase and cyclooxygenase-2 protein expressions. α-Bungarotoxin, the specific α7-nAChR antagonist, inhibited these biological effects. However, 5-lipoxygenase inhibition had no effect on α7-nAChR mRNA expression, but significantly inhibited cell proliferation and activation of NF-κB and cyclooxygenase-2, whereas NF-κB-specific inhibitor caffeic acid phenethyl ester reduced both cell proliferation and cyclooxygenase expression induced by NNK without affecting α7-nAChR mRNA level and 5-lipoxygenase expression. Together, the present study demonstrated that NNK promoted colon cancer growth in vitro. NF-κB not only conveys the biological effect of α7-nAChR activation but is also involved in the cross-talk between 5-lipoxygenase and cyclooxygenase-2 in response to NNK in colon cancer cell development.
Persistent Identifierhttp://hdl.handle.net/10722/207512
ISSN
2015 Impact Factor: 3.76
2015 SCImago Journal Rankings: 1.847

 

DC FieldValueLanguage
dc.contributor.authorYe, Yini-
dc.contributor.authorLiu, Edgar Shiu Lam-
dc.contributor.authorShin, Vivianyvonne-
dc.contributor.authorWu, William Ka Kei-
dc.contributor.authorCho, Chihin-
dc.date.accessioned2014-12-31T01:01:48Z-
dc.date.available2014-12-31T01:01:48Z-
dc.date.issued2004-
dc.identifier.citationJournal of Pharmacology and Experimental Therapeutics, 2004, v. 311, n. 1, p. 123-130-
dc.identifier.issn0022-3565-
dc.identifier.urihttp://hdl.handle.net/10722/207512-
dc.description.abstract4-(N-Methyl-N-nitrosamino)-1-(3-pyridyl)-1-butanone (NNK), the tobacco-specific nitrosamine, induces lung cancer in all animal species tested and is thought to contribute significantly to the high lung cancer burden associated with smoking. However, there is no report whether NNK could promote colon cancer growth. To address this hypothesis and the possible signaling pathways involved, we used SW1116 colon cancer cell line to study these biological events in vitro. Results showed that NNK, after 5-h treatment, stimulated cell proliferation, enhanced α7-nicotinic acetylcholine receptor (α7-nAChR) mRNA levels and nuclear factor-κB (NF-κB) DNA binding activity, as well as 5-lipoxygenase and cyclooxygenase-2 protein expressions. α-Bungarotoxin, the specific α7-nAChR antagonist, inhibited these biological effects. However, 5-lipoxygenase inhibition had no effect on α7-nAChR mRNA expression, but significantly inhibited cell proliferation and activation of NF-κB and cyclooxygenase-2, whereas NF-κB-specific inhibitor caffeic acid phenethyl ester reduced both cell proliferation and cyclooxygenase expression induced by NNK without affecting α7-nAChR mRNA level and 5-lipoxygenase expression. Together, the present study demonstrated that NNK promoted colon cancer growth in vitro. NF-κB not only conveys the biological effect of α7-nAChR activation but is also involved in the cross-talk between 5-lipoxygenase and cyclooxygenase-2 in response to NNK in colon cancer cell development.-
dc.languageeng-
dc.relation.ispartofJournal of Pharmacology and Experimental Therapeutics-
dc.titleThe modulating role of nuclear factor-κB in the action of α7-nicotinic acetylcholine receptor and cross-talk between 5-lipoxygenase and cyclooxygenase-2 in colon cancer growth induced by 4-(N-methyl-N- nitrosamino)-1-(3-pyridyl)-1-butanone-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1124/jpet.104.068031-
dc.identifier.pmid15161935-
dc.identifier.scopuseid_2-s2.0-4644359715-
dc.identifier.volume311-
dc.identifier.issue1-
dc.identifier.spage123-
dc.identifier.epage130-

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