Source:http://linkedlifedata.com/resource/pubmed/id/10646901
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
|
pubmed:dateCreated |
2000-2-4
|
pubmed:databankReference | |
pubmed:abstractText |
The expression of the BCL-2 family proteins, BCL-2, BAX, BCL(XL) and BAK have been determined in a panel of 12 human ovarian carcinoma cell lines encompassing a wide range in sensitivity to cisplatin. Whereas BAX, BCL(XL) and BAK levels did not correlate with sensitivity, there was a statistically significant inverse correlation (r = -0.81; P = 0.002) between growth inhibition by cisplatin and BCL-2 levels. In sublines possessing acquired resistance to various platinum-based drugs or across a panel of human ovarian carcinoma xenografts, there was no consistent pattern of BCL-2 expression. Two relatively sensitive lines (A2780 and CH1) have been stably transfected with bcl-2 and bcl(XL) respectively and two relatively resistant lines (A2780cisR and SKOV-3) stably transfected with bax. Overexpression of BCL-2 in A2780 cells led to resistance to cisplatin compared to the vector control when assayed at 48 h post-drug incubation but a significant increase in sensitivity at 96 h. Relative rates of apoptosis at 48- and 96-h post-cisplatin exposure mirrored the growth inhibition. There was no significant difference in sensitivity of the pair of lines by clonogenic assay. No significant changes in chemosensitivity to a variety of DNA-damaging or tubulin-interactive agents were observed in the remaining transfected lines. Taken together, these results suggest that, in human ovarian carcinoma cells, high BCL-2 levels (either naturally occurring or through gene transfection) confers a trend towards sensitivity not resistance to platinum drugs.
|
pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/10646901-1586979,
http://linkedlifedata.com/resource/pubmed/commentcorrection/10646901-1617660,
http://linkedlifedata.com/resource/pubmed/commentcorrection/10646901-1854622,
http://linkedlifedata.com/resource/pubmed/commentcorrection/10646901-7478541,
http://linkedlifedata.com/resource/pubmed/commentcorrection/10646901-7585531,
http://linkedlifedata.com/resource/pubmed/commentcorrection/10646901-8427780,
http://linkedlifedata.com/resource/pubmed/commentcorrection/10646901-8599870,
http://linkedlifedata.com/resource/pubmed/commentcorrection/10646901-8616869,
http://linkedlifedata.com/resource/pubmed/commentcorrection/10646901-8752171,
http://linkedlifedata.com/resource/pubmed/commentcorrection/10646901-9472630,
http://linkedlifedata.com/resource/pubmed/commentcorrection/10646901-9584207
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Jan
|
pubmed:issn |
0007-0920
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
82
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
436-40
|
pubmed:dateRevised |
2009-11-18
|
pubmed:meshHeading |
pubmed-meshheading:10646901-Antineoplastic Agents,
pubmed-meshheading:10646901-Apoptosis,
pubmed-meshheading:10646901-Base Sequence,
pubmed-meshheading:10646901-Cisplatin,
pubmed-meshheading:10646901-DNA Damage,
pubmed-meshheading:10646901-Drug Resistance, Neoplasm,
pubmed-meshheading:10646901-Female,
pubmed-meshheading:10646901-Genes, bcl-2,
pubmed-meshheading:10646901-Humans,
pubmed-meshheading:10646901-Molecular Sequence Data,
pubmed-meshheading:10646901-Ovarian Neoplasms,
pubmed-meshheading:10646901-Transplantation, Heterologous,
pubmed-meshheading:10646901-Tumor Cells, Cultured
|
pubmed:year |
2000
|
pubmed:articleTitle |
BCL-2 family protein expression and platinum drug resistance in ovarian carcinoma.
|
pubmed:affiliation |
CRC Centre for Cancer Therapeutics, Institute of Cancer Research, Belmont, Sutton, UK.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|