Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2005-1-5
pubmed:abstractText
Hepatocellular carcinoma (HCC) is one of the most common human malignancies. Its high mortality rate is mainly a result of high intrahepatic recurrence. The novel synthetic retinoid acyclic retinoid (ACR) has been reported to prevent the recurrence of human HCC after surgical resection of primary tumors, but the molecular mechanisms underlying its effects remain to be elucidated. In this study, we clarified the molecular targets of ACR.
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0016-5085
pubmed:author
pubmed:issnType
Print
pubmed:volume
128
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
86-95
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:15633126-Antineoplastic Agents, pubmed-meshheading:15633126-Carcinoma, Hepatocellular, pubmed-meshheading:15633126-Cell Line, Tumor, pubmed-meshheading:15633126-Cell Proliferation, pubmed-meshheading:15633126-Down-Regulation, pubmed-meshheading:15633126-Fibroblast Growth Factors, pubmed-meshheading:15633126-Gene Expression, pubmed-meshheading:15633126-Humans, pubmed-meshheading:15633126-Liver Neoplasms, pubmed-meshheading:15633126-Neoplasm Recurrence, Local, pubmed-meshheading:15633126-Oligonucleotide Array Sequence Analysis, pubmed-meshheading:15633126-Protein-Tyrosine Kinases, pubmed-meshheading:15633126-Receptor, Fibroblast Growth Factor, Type 3, pubmed-meshheading:15633126-Receptors, Fibroblast Growth Factor, pubmed-meshheading:15633126-Signal Transduction, pubmed-meshheading:15633126-Tretinoin, pubmed-meshheading:15633126-rho GTP-Binding Proteins
pubmed:year
2005
pubmed:articleTitle
Acyclic retinoid inhibits human hepatoma cell growth by suppressing fibroblast growth factor-mediated signaling pathways.
pubmed:affiliation
Department of Gastroenterology, Graduate School of Medicine, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8655, Japan.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't