pubmed-article:18047722 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:18047722 | lifeskim:mentions | umls-concept:C0522466 | lld:lifeskim |
pubmed-article:18047722 | lifeskim:mentions | umls-concept:C1882726 | lld:lifeskim |
pubmed-article:18047722 | lifeskim:mentions | umls-concept:C1707455 | lld:lifeskim |
pubmed-article:18047722 | lifeskim:mentions | umls-concept:C1956267 | lld:lifeskim |
pubmed-article:18047722 | lifeskim:mentions | umls-concept:C0205349 | lld:lifeskim |
pubmed-article:18047722 | lifeskim:mentions | umls-concept:C0073363 | lld:lifeskim |
pubmed-article:18047722 | pubmed:dateCreated | 2007-11-30 | lld:pubmed |
pubmed-article:18047722 | pubmed:abstractText | Comfrey (Symphytum officinale) is a perennial plant and has been consumed by humans as a vegetable, a tea and an herbal medicine for more than 2000 years. It, however, is hepatotoxic and carcinogenic in experimental animals and hepatotoxic in humans. Pyrrolizidine alkaloids (PAs) exist in many plants and many of them cause liver toxicity and/or cancer in humans and experimental animals. In our previous study, we found that the mutagenicity of comfrey was associated with the PAs contained in the plant. Therefore, we suggest that carcinogenicity of comfrey result from those PAs. To confirm our hypothesis, we compared the expression of genes and processes of biological functions that were altered by comfrey (mixture of the plant with PAs) and riddelliine (a prototype of carcinogenic PA) in rat liver for carcinogenesis in this study. | lld:pubmed |
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pubmed-article:18047722 | pubmed:language | eng | lld:pubmed |
pubmed-article:18047722 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18047722 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:18047722 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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pubmed-article:18047722 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:18047722 | pubmed:issn | 1471-2105 | lld:pubmed |
pubmed-article:18047722 | pubmed:author | pubmed-author:PanM JMJ | lld:pubmed |
pubmed-article:18047722 | pubmed:author | pubmed-author:DaiS JSJ | lld:pubmed |
pubmed-article:18047722 | pubmed:author | pubmed-author:ChenTaoT | lld:pubmed |
pubmed-article:18047722 | pubmed:author | pubmed-author:FuscoeJamesJ | lld:pubmed |
pubmed-article:18047722 | pubmed:author | pubmed-author:DialStaceyS | lld:pubmed |
pubmed-article:18047722 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:18047722 | pubmed:volume | 8 Suppl 7 | lld:pubmed |
pubmed-article:18047722 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:18047722 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:18047722 | pubmed:pagination | S22 | lld:pubmed |
pubmed-article:18047722 | pubmed:dateRevised | 2010-9-16 | lld:pubmed |
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pubmed-article:18047722 | pubmed:meshHeading | pubmed-meshheading:18047722... | lld:pubmed |
pubmed-article:18047722 | pubmed:year | 2007 | lld:pubmed |
pubmed-article:18047722 | pubmed:articleTitle | Comparison of gene expression profiles altered by comfrey and riddelliine in rat liver. | lld:pubmed |
pubmed-article:18047722 | pubmed:affiliation | Division of Systems Toxicology, National Center for Toxicological Research, FDA, Jefferson, AR 72079, USA. lei.guo@fda.hhs.gov | lld:pubmed |
pubmed-article:18047722 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:18047722 | pubmed:publicationType | Comparative Study | lld:pubmed |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:18047722 | lld:pubmed |