Source:http://linkedlifedata.com/resource/pubmed/id/20926293
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rdf:type | |
lifeskim:mentions |
umls-concept:C0007634,
umls-concept:C0007935,
umls-concept:C0015127,
umls-concept:C0079395,
umls-concept:C0086418,
umls-concept:C0151686,
umls-concept:C0152013,
umls-concept:C0237477,
umls-concept:C0596402,
umls-concept:C0598934,
umls-concept:C1314792,
umls-concept:C1515655,
umls-concept:C1533691,
umls-concept:C1704259,
umls-concept:C1705987
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pubmed:issue |
22
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pubmed:dateCreated |
2010-10-19
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pubmed:abstractText |
The present Letter identified 2'-hydroxy-2,3,4',6'-tetramethoxychalcone (HTMC) as a potent in vitro cytotoxic agent with selective activity against cell lines derived from human lung cancer. In A549 lung adenocarcinoma cells, HTMC caused G1 phase cell-cycle arrest. HTMC treatment also led to an inhibition of cell-cycle regulatory proteins phosphorylation of cdc2 (Tyr(15) and Tyr(161)) and Rb (Ser(795) and Ser(807/811)), which was accompanied by the accumulation of tumor suppressor genes p53 and p21. In addition, in vivo data demonstrated that HTMC act as a tumor growth suppressing agent.
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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 |
Nov
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pubmed:issn |
1464-3405
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pubmed:author | |
pubmed:copyrightInfo |
Copyright © 2010 Elsevier Ltd. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:day |
15
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pubmed:volume |
20
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
6508-12
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pubmed:meshHeading |
pubmed-meshheading:20926293-Adenocarcinoma,
pubmed-meshheading:20926293-Antineoplastic Agents,
pubmed-meshheading:20926293-Cell Cycle Proteins,
pubmed-meshheading:20926293-Cell Division,
pubmed-meshheading:20926293-Cell Line, Tumor,
pubmed-meshheading:20926293-G1 Phase,
pubmed-meshheading:20926293-Genes, p53,
pubmed-meshheading:20926293-Humans,
pubmed-meshheading:20926293-Lung Neoplasms,
pubmed-meshheading:20926293-Phosphorylation
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pubmed:year |
2010
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pubmed:articleTitle |
Chalcone HTMC causes in vitro selective cytotoxicity, cell-cycle G1 phase arrest through p53-dependent pathway in human lung adenocarcinoma A549 cells, and in vivo tumor growth suppression.
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pubmed:affiliation |
Institute of Biochemical Sciences and Technology, Chaoyang University of Technology, Wufeng, Taiwan, ROC.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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