Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:18187174rdf:typepubmed:Citationlld:pubmed
pubmed-article:18187174lifeskim:mentionsumls-concept:C0086418lld:lifeskim
pubmed-article:18187174lifeskim:mentionsumls-concept:C1711178lld:lifeskim
pubmed-article:18187174lifeskim:mentionsumls-concept:C0596290lld:lifeskim
pubmed-article:18187174lifeskim:mentionsumls-concept:C1420433lld:lifeskim
pubmed-article:18187174lifeskim:mentionsumls-concept:C1424666lld:lifeskim
pubmed-article:18187174lifeskim:mentionsumls-concept:C1415887lld:lifeskim
pubmed-article:18187174lifeskim:mentionsumls-concept:C1419040lld:lifeskim
pubmed-article:18187174lifeskim:mentionsumls-concept:C0598086lld:lifeskim
pubmed-article:18187174lifeskim:mentionsumls-concept:C0598388lld:lifeskim
pubmed-article:18187174lifeskim:mentionsumls-concept:C1704259lld:lifeskim
pubmed-article:18187174lifeskim:mentionsumls-concept:C1705987lld:lifeskim
pubmed-article:18187174lifeskim:mentionsumls-concept:C0205263lld:lifeskim
pubmed-article:18187174pubmed:issue1lld:pubmed
pubmed-article:18187174pubmed:dateCreated2008-3-21lld:pubmed
pubmed-article:18187174pubmed:abstractTextLung cancer is the leading cause of cancer deaths worldwide. Epidemiological studies have shown that exposure to cooking oil fumes (COF) is a risk factor for lung cancer. Trans, trans-2,4-decadienal (tt-DDE), a dienaldehyde, is abundant in heated oils and COF. Previously, we found that long-term exposure (45 days) to a sub-lethal dose (1 microM) of tt-DDE significantly increased growth of human bronchial epithelial cells (BEAS-2B). Aims of this study are to understand the mechanism of tt-DDE-induced cell proliferation and possible protective effects of antioxidant, vitamin C and N-acetylcysteine (NAC) in BEAS-2B cells. Utilizing the real-time RT-PCR and Western immunoblotting, we found that p27 mRNA and protein levels were significantly increased by 1 microM tt-DDE treatment. Co-treatment with vitamin C or NAC partially prevented tt-DDE-induced cell proliferation. In addition, the downstream targets of p27, including CDK4, cyclin D1 and phosphorylated-Rb proteins, increased in 1 microM tt-DDE-treated cells and these changes were prevented by NAC co-treatment. Therefore, these results suggest that tt-DDE increased cell proliferation via inhibition of p27 expression, increase in CDK4/cyclin D1 protein accumulation and enhancement of Rb phosphorylation. Increased cell proliferation is considered as the early stages of lung carcinogenesis. Administration of antioxidants may prevent COF-associated lung carcinogenesis.lld:pubmed
pubmed-article:18187174pubmed:languageenglld:pubmed
pubmed-article:18187174pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:18187174pubmed:citationSubsetIMlld:pubmed
pubmed-article:18187174pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:18187174pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:18187174pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:18187174pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:18187174pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:18187174pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:18187174pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:18187174pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:18187174pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:18187174pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:18187174pubmed:statusMEDLINElld:pubmed
pubmed-article:18187174pubmed:monthAprlld:pubmed
pubmed-article:18187174pubmed:issn0041-008Xlld:pubmed
pubmed-article:18187174pubmed:authorpubmed-author:LinPinpinPlld:pubmed
pubmed-article:18187174pubmed:authorpubmed-author:ChangYun-Chin...lld:pubmed
pubmed-article:18187174pubmed:issnTypePrintlld:pubmed
pubmed-article:18187174pubmed:day1lld:pubmed
pubmed-article:18187174pubmed:volume228lld:pubmed
pubmed-article:18187174pubmed:ownerNLMlld:pubmed
pubmed-article:18187174pubmed:authorsCompleteYlld:pubmed
pubmed-article:18187174pubmed:pagination76-83lld:pubmed
pubmed-article:18187174pubmed:dateRevised2009-11-19lld:pubmed
pubmed-article:18187174pubmed:meshHeadingpubmed-meshheading:18187174...lld:pubmed
pubmed-article:18187174pubmed:meshHeadingpubmed-meshheading:18187174...lld:pubmed
pubmed-article:18187174pubmed:meshHeadingpubmed-meshheading:18187174...lld:pubmed
pubmed-article:18187174pubmed:meshHeadingpubmed-meshheading:18187174...lld:pubmed
pubmed-article:18187174pubmed:meshHeadingpubmed-meshheading:18187174...lld:pubmed
pubmed-article:18187174pubmed:meshHeadingpubmed-meshheading:18187174...lld:pubmed
pubmed-article:18187174pubmed:meshHeadingpubmed-meshheading:18187174...lld:pubmed
pubmed-article:18187174pubmed:meshHeadingpubmed-meshheading:18187174...lld:pubmed
pubmed-article:18187174pubmed:meshHeadingpubmed-meshheading:18187174...lld:pubmed
pubmed-article:18187174pubmed:meshHeadingpubmed-meshheading:18187174...lld:pubmed
pubmed-article:18187174pubmed:meshHeadingpubmed-meshheading:18187174...lld:pubmed
pubmed-article:18187174pubmed:meshHeadingpubmed-meshheading:18187174...lld:pubmed
pubmed-article:18187174pubmed:meshHeadingpubmed-meshheading:18187174...lld:pubmed
pubmed-article:18187174pubmed:meshHeadingpubmed-meshheading:18187174...lld:pubmed
pubmed-article:18187174pubmed:meshHeadingpubmed-meshheading:18187174...lld:pubmed
pubmed-article:18187174pubmed:meshHeadingpubmed-meshheading:18187174...lld:pubmed
pubmed-article:18187174pubmed:meshHeadingpubmed-meshheading:18187174...lld:pubmed
pubmed-article:18187174pubmed:meshHeadingpubmed-meshheading:18187174...lld:pubmed
pubmed-article:18187174pubmed:meshHeadingpubmed-meshheading:18187174...lld:pubmed
pubmed-article:18187174pubmed:meshHeadingpubmed-meshheading:18187174...lld:pubmed
pubmed-article:18187174pubmed:meshHeadingpubmed-meshheading:18187174...lld:pubmed
pubmed-article:18187174pubmed:meshHeadingpubmed-meshheading:18187174...lld:pubmed
pubmed-article:18187174pubmed:year2008lld:pubmed
pubmed-article:18187174pubmed:articleTitleTrans, trans-2,4-decadienal induced cell proliferation via p27 pathway in human bronchial epithelial cells.lld:pubmed
pubmed-article:18187174pubmed:affiliationInstitute of Biochemistry and Biotechnology, Chung Shan Medical University, Taichung, Taiwan.lld:pubmed
pubmed-article:18187174pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:18187174pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed