Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
7
pubmed:dateCreated
2011-2-14
pubmed:abstractText
Discovery of the molecular targets of traditional medicine and its chemical footprints can validate the use of such medicine. In the present report, we investigated the effect of ursolic acid (UA), a pentacyclic triterpenoid found in rosemary and holy basil, on apoptosis induced by TRAIL. We found that UA potentiated TRAIL-induced apoptosis in cancer cells. In addition, UA also sensitized TRAIL-resistant cancer cells to the cytokine. When we investigated the mechanism, we found that UA down-regulated cell survival proteins and induced the cell surface expression of both TRAIL receptors, death receptors 4 and 5 (DR4 and -5). Induction of receptors by UA occurred independently of cell type. Gene silencing of either receptor by small interfering RNA reduced the apoptosis induced by UA and the effect of TRAIL. In addition, UA also decreased the expression of decoy receptor 2 (DcR2) but not DcR1. Induction of DRs was independent of p53 because UA induced DR4 and DR5 in HCT116 p53(-/-) cells. Induction of DRs, however, was dependent on JNK because UA induced JNK, and its pharmacologic inhibition abolished the induction of the receptors. The down-regulation of survival proteins and up-regulation of the DRs required reactive oxygen species (ROS) because UA induced ROS, and its quenching abolished the effect of the terpene. Also, potentiation of TRAIL-induced apoptosis by UA was significantly reduced by both ROS quenchers and JNK inhibitor. In addition, UA was also found to induce the expression of DRs, down-regulate cell survival proteins, and activate JNK in orthotopically implanted human colorectal cancer in a nude mouse model. Overall, our results showed that UA potentiates TRAIL-induced apoptosis through activation of ROS and JNK-mediated up-regulation of DRs and down-regulation of DcR2 and cell survival proteins.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Antineoplastic Agents, Phytogenic, http://linkedlifedata.com/resource/pubmed/chemical/MAP Kinase Kinase 4, http://linkedlifedata.com/resource/pubmed/chemical/Reactive Oxygen Species, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, TNF-Related..., http://linkedlifedata.com/resource/pubmed/chemical/TNF-Related Apoptosis-Inducing..., http://linkedlifedata.com/resource/pubmed/chemical/TNFRSF10A protein, human, http://linkedlifedata.com/resource/pubmed/chemical/TNFRSF10D protein, human, http://linkedlifedata.com/resource/pubmed/chemical/TNFSF10 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/TP53 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Triterpenes, http://linkedlifedata.com/resource/pubmed/chemical/Tumor Necrosis Factor Decoy..., http://linkedlifedata.com/resource/pubmed/chemical/Tumor Suppressor Protein p53, http://linkedlifedata.com/resource/pubmed/chemical/ursolic acid
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
1083-351X
pubmed:author
pubmed:issnType
Electronic
pubmed:day
18
pubmed:volume
286
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
5546-57
pubmed:meshHeading
pubmed-meshheading:21156789-Animals, pubmed-meshheading:21156789-Antineoplastic Agents, Phytogenic, pubmed-meshheading:21156789-Apoptosis, pubmed-meshheading:21156789-Caco-2 Cells, pubmed-meshheading:21156789-Cell Survival, pubmed-meshheading:21156789-Colorectal Neoplasms, pubmed-meshheading:21156789-Down-Regulation, pubmed-meshheading:21156789-Drug Synergism, pubmed-meshheading:21156789-Humans, pubmed-meshheading:21156789-MAP Kinase Kinase 4, pubmed-meshheading:21156789-Mice, pubmed-meshheading:21156789-Mice, Nude, pubmed-meshheading:21156789-Neoplasm Transplantation, pubmed-meshheading:21156789-Reactive Oxygen Species, pubmed-meshheading:21156789-Receptors, TNF-Related Apoptosis-Inducing Ligand, pubmed-meshheading:21156789-TNF-Related Apoptosis-Inducing Ligand, pubmed-meshheading:21156789-Triterpenes, pubmed-meshheading:21156789-Tumor Necrosis Factor Decoy Receptors, pubmed-meshheading:21156789-Tumor Suppressor Protein p53, pubmed-meshheading:21156789-Up-Regulation, pubmed-meshheading:21156789-Xenograft Model Antitumor Assays
pubmed:year
2011
pubmed:articleTitle
Ursolic acid, a pentacyclin triterpene, potentiates TRAIL-induced apoptosis through p53-independent up-regulation of death receptors: evidence for the role of reactive oxygen species and JNK.
pubmed:affiliation
Cytokine Research Laboratory, Department of Experimental Therapeutics, University of Texas MD Anderson Cancer Center, Houston, Texas 77030, USA.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural