Source:http://linkedlifedata.com/resource/pubmed/id/18163538
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2008-1-17
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pubmed:abstractText |
A series of substituted 9-aminoacridines is evaluated for antiproliferative activity toward pancreatic cancer cells. The results indicate that the compounds inhibit cell proliferation by inducing a G1-S phase arrest. A model is also developed that explains the molecular basis to inhibition through a DNA "threading" mechanism. We conclude that the drug-DNA complex formed blocks topoisomerase II binding and activity leading to catalytic inhibition of the enzyme and the induction of apoptosis and programmed cell death.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
0022-2623
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
24
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pubmed:volume |
51
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
179-82
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pubmed:dateRevised |
2010-12-3
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pubmed:meshHeading |
pubmed-meshheading:18163538-Aminoacridines,
pubmed-meshheading:18163538-Antineoplastic Agents,
pubmed-meshheading:18163538-Apoptosis,
pubmed-meshheading:18163538-Cell Cycle,
pubmed-meshheading:18163538-Cell Line, Tumor,
pubmed-meshheading:18163538-Cell Proliferation,
pubmed-meshheading:18163538-DNA,
pubmed-meshheading:18163538-Drug Screening Assays, Antitumor,
pubmed-meshheading:18163538-Humans,
pubmed-meshheading:18163538-Models, Molecular,
pubmed-meshheading:18163538-Pancreatic Neoplasms,
pubmed-meshheading:18163538-Structure-Activity Relationship,
pubmed-meshheading:18163538-Topoisomerase II Inhibitors
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pubmed:year |
2008
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pubmed:articleTitle |
Acridine-based agents with topoisomerase II activity inhibit pancreatic cancer cell proliferation and induce apoptosis.
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pubmed:affiliation |
Department of Medicinal Chemistry, University of Minnesota, Minneapolis, Minnesota 55455, USA.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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