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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1-2
pubmed:dateCreated
2011-1-10
pubmed:abstractText
Boswellic acids have invariably been reported for their antiproliferative potential in various cell systems. In the present study the growth inhibitory effect of propionyloxy derivative of 11-keto-?-boswellic acid (PKBA; a semisynthetic analogue of 11-keto-?-boswellic acid) on HL-60 promyelocytic leukemia cells is being reported for the first time. In the preliminary studies, in vitro cytotoxicity of PKBA was investigated against eight human cancer cell lines viz., IMR-32, SF-295 (both neuroblastoma), PC-3 (prostate), Colo-205 (colon), MCF-7 (breast), OVCAR-5 (ovary), HL-60, Molt-4 (both leukemia) and their respective IC(50) values were found to be 5.95, 7.11, 15.2, 14.5, 15, 15.9, 8.7 & 9.5?g/ml, respectively. For determining the mechanism of cell death in HL-60 cells, PKBA was subjected to different mechanistic studies. DNA relaxation assay of PKBA revealed inhibition of both topoisomerases I & II. The fragmentation analysis of DNA revealed typical ladders indicating the cytotoxic effect to be mediated by induction of apoptosis. The morphologic studies of PKBA showed the presence of true apoptotic bodies. Apoptosis was confirmed further by flow-cytometric detection of sub-G(1) peaks and enhanced annexin-V-FITC binding of the cells. The activation of apoptotic cascade by PKBA in HL-60 cells was found to be associated with the loss of mitochondrial membrane potential, release of cytochrome c, activation of initiator and executioner caspases and cleavage of poly ADP ribose polymerase (PARP). In vivo studies of PKBA revealed anti-tumoral activity against both ascitic and solid murine tumor models. These studies thus demonstrate PKBA to induce apoptosis in HL-60 cells due to the inhibition of topoisomerases I and II.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
1872-7786
pubmed:author
pubmed:copyrightInfo
Copyright © 2010 Elsevier Ireland Ltd. All rights reserved.
pubmed:issnType
Electronic
pubmed:day
15
pubmed:volume
189
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
60-71
pubmed:meshHeading
pubmed-meshheading:21056033-Animals, pubmed-meshheading:21056033-Apoptosis, pubmed-meshheading:21056033-Cell Proliferation, pubmed-meshheading:21056033-Comet Assay, pubmed-meshheading:21056033-DNA Damage, pubmed-meshheading:21056033-DNA Topoisomerases, Type I, pubmed-meshheading:21056033-DNA Topoisomerases, Type II, pubmed-meshheading:21056033-Flow Cytometry, pubmed-meshheading:21056033-HL-60 Cells, pubmed-meshheading:21056033-Humans, pubmed-meshheading:21056033-Magnetic Resonance Spectroscopy, pubmed-meshheading:21056033-Male, pubmed-meshheading:21056033-Membrane Potential, Mitochondrial, pubmed-meshheading:21056033-Mice, pubmed-meshheading:21056033-Microscopy, Electron, Scanning, pubmed-meshheading:21056033-Propionates, pubmed-meshheading:21056033-Random Allocation, pubmed-meshheading:21056033-Spectrometry, Mass, Electrospray Ionization, pubmed-meshheading:21056033-Topoisomerase Inhibitors, pubmed-meshheading:21056033-Triterpenes
pubmed:year
2011
pubmed:articleTitle
A propionyloxy derivative of 11-keto-?-boswellic acid induces apoptosis in HL-60 cells mediated through topoisomerase I & II inhibition.
pubmed:affiliation
Pharmacology Division, Indian Institute of Integrative Medicine, Canal Road, Jammu tawi, Jammu and Kashmir, India.
pubmed:publicationType
Journal Article