Source:http://linkedlifedata.com/resource/pubmed/id/12482336
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rdf:type | |
lifeskim:mentions |
umls-concept:C0007102,
umls-concept:C0007634,
umls-concept:C0012920,
umls-concept:C0016360,
umls-concept:C0017262,
umls-concept:C0040085,
umls-concept:C0086418,
umls-concept:C0123931,
umls-concept:C0185117,
umls-concept:C0205195,
umls-concept:C0205210,
umls-concept:C1155872,
umls-concept:C1709059,
umls-concept:C2347946,
umls-concept:C2911684
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pubmed:issue |
3
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pubmed:dateCreated |
2002-12-16
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pubmed:abstractText |
This study was designed to explore the possible interaction of 5-fluorouracil (5-FU) and 7-ethyl-10-hydroxycamptothecin (SN-38) in vitro. Human colon cancer LoVo cells were treated in both a dose- and time-dependent manner using clinically relevant concentrations of and exposure to 5-FU and/or SN-38. The expression of thymidylate synthase (TS), topoisomerase I, and cell cycle kinetics were evaluated by Western blot analysis and flow cytometry, respectively. Cytotoxicity was evaluated by MTT (3-[4,5-dimethylthiazol-2yl]-2,5-diphenyl tetrazolium bromide) assay. The cytotoxic effects of combination treatment were determined by median effect analysis. Topoisomerase I expression was downregulated following 12 hours of exposure to treatment, and topoisomerase I expression recovered 8 hours after SN-38 was removed. The TS expression was decreased following 24 hours of 5-FU and it remained at reduced levels for > 24 hours after removal of 5-FU. SN-38 induced an arrest at S/G2/M phase, reaching its maximum effect at 12 hours. This cell cycle arrest was reversed 24 hours after SN-38 was removed. 5-FU induced an arrest at the S phase, and maximum arrest occurred at 12 hours and lasted for > 48 hours. After 12 hours of sequential SN-38, LoVo cells were arrested in S phase, thereby potentiating the effect of 5-FU. Cytotoxicity studies confirmed the synergistic interaction between 5-FU and irinotecan. These findings suggest that the proper sequencing of 5-FU/irinotecan depends on regulation of topoisomerase I, and cell cycle kinetics
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Camptothecin,
http://linkedlifedata.com/resource/pubmed/chemical/Fluorouracil,
http://linkedlifedata.com/resource/pubmed/chemical/Thymidylate Synthase,
http://linkedlifedata.com/resource/pubmed/chemical/Topoisomerase I Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/irinotecan
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
1533-0028
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
2
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
182-8
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:12482336-Antineoplastic Combined Chemotherapy Protocols,
pubmed-meshheading:12482336-Camptothecin,
pubmed-meshheading:12482336-Cell Cycle,
pubmed-meshheading:12482336-Colonic Neoplasms,
pubmed-meshheading:12482336-Dose-Response Relationship, Drug,
pubmed-meshheading:12482336-Fluorouracil,
pubmed-meshheading:12482336-Humans,
pubmed-meshheading:12482336-Thymidylate Synthase,
pubmed-meshheading:12482336-Topoisomerase I Inhibitors,
pubmed-meshheading:12482336-Tumor Cells, Cultured
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pubmed:year |
2002
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pubmed:articleTitle |
Combination of 5-fluorouracil and irinotecan on modulation of thymidylate synthase and topoisomerase I expression and cell cycle regulation in human colon cancer LoVo cells: clinical relevance.
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pubmed:affiliation |
Beijing 307 Hospital Cancer Center, China.
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pubmed:publicationType |
Journal Article,
In Vitro,
Research Support, Non-U.S. Gov't
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