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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
8
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pubmed:dateCreated |
1997-6-17
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pubmed:abstractText |
The transforming growth factor-beta (TGF-beta) family of regulatory growth factors can reversibly arrest cell division in the G1 phase of the cell cycle. Previously, TGF-beta3 was shown to protect epithelial cells and hematopoietic cells from cytotoxic damage in vitro and in vivo, and to reduce the severity and duration of oral mucositis induced by 5-fluorouracil (5-FU) in vivo. In the present study, we tested whether TGF-beta3 can protect epithelial cells from a range of chemotherapy drugs with differing mechanisms of action, using the CCL64 cell line as a model system. We report that preincubation of cells with TGF-beta3 for 24 hr resulted in enhanced clonogenicity following exposure to vinblastine, vincristine, etoposide, taxol, ara-C, methotrexate, or 5-FU. Protection was measured in colony-forming assays, which demonstrated that the protected cells could re-enter the cell cycle and undergo multiple rounds of cell division. At high cytotoxic drug concentrations, absolute colony counts were increased for the cultures prearrested by TGF-beta3, as compared with the proliferating control cultures. The effects of TGF-beta3 were reduced for cisplatin and doxorubicin, drugs that are toxic to cells throughout the cell cycle. Thus, TGF-beta3 can effectively reduce the cytotoxicity of anticancer drugs that act predominantly in S or M phase of the cell cycle.
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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/Antimetabolites, Antineoplastic,
http://linkedlifedata.com/resource/pubmed/chemical/Antineoplastic Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Antineoplastic Agents, Phytogenic,
http://linkedlifedata.com/resource/pubmed/chemical/Transforming Growth Factor beta
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0006-2952
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
25
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pubmed:volume |
53
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1149-59
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pubmed:dateRevised |
2003-11-14
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pubmed:meshHeading |
pubmed-meshheading:9175720-Animals,
pubmed-meshheading:9175720-Antimetabolites, Antineoplastic,
pubmed-meshheading:9175720-Antineoplastic Agents,
pubmed-meshheading:9175720-Antineoplastic Agents, Phytogenic,
pubmed-meshheading:9175720-Cell Cycle,
pubmed-meshheading:9175720-Cell Survival,
pubmed-meshheading:9175720-Cells, Cultured,
pubmed-meshheading:9175720-Dose-Response Relationship, Drug,
pubmed-meshheading:9175720-Epithelium,
pubmed-meshheading:9175720-Mink,
pubmed-meshheading:9175720-S Phase,
pubmed-meshheading:9175720-Transforming Growth Factor beta
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pubmed:year |
1997
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pubmed:articleTitle |
Transforming growth factor-beta3 protection of epithelial cells from cycle-selective chemotherapy in vitro.
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pubmed:affiliation |
Oncogene Science Inc., Pharmaceuticals Division, Uniondale, NY 11553-3649, U.S.A.
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pubmed:publicationType |
Journal Article
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