Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
19
pubmed:dateCreated
1998-12-10
pubmed:abstractText
Although paclitaxel is an important chemotherapy agent for the treatment of patients with epithelial ovarian cancer, its utility is significantly limited by the frequent development of drug resistance. Recent evidence suggests that resistance to chemotherapy may be partly related to defects in the apoptotic pathway. In this study we have investigated whether enhancement of apoptotic pathway function through stable expression of the BAD protein is capable of sensitizing human epithelial ovarian cancer cells to the effects of chemotherapy. Expression of HA-BAD in six separate clonal transfectants from two different ovarian cancer cell lines was found to significantly enhance the cytotoxic effects of paclitaxel, vincristine, and, to a lesser extent, etoposide. Enhancement of paclitaxel-induced apoptosis in HA-BAD-expressing clones was demonstrated by trypan blue exclusion, clonogenic cell assay, and flow cytometric evaluation. Importantly, this effect was associated with binding of HA-BAD to BCL-xL and concomitant disruption of BAX:BCL-xL interaction. Taken together, these data suggest that the development of small molecules which mimic the effects of BAD may represent a new class of drugs capable of preventing or reversing resistance to chemotherapy agents such as paclitaxel.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
0950-9232
pubmed:author
pubmed:issnType
Print
pubmed:day
12
pubmed:volume
17
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2419-27
pubmed:dateRevised
2007-11-15
pubmed:meshHeading
pubmed-meshheading:9824152-Animals, pubmed-meshheading:9824152-Antineoplastic Agents, Phytogenic, pubmed-meshheading:9824152-Apoptosis, pubmed-meshheading:9824152-Ascitic Fluid, pubmed-meshheading:9824152-Carrier Proteins, pubmed-meshheading:9824152-Clone Cells, pubmed-meshheading:9824152-DNA, Neoplasm, pubmed-meshheading:9824152-Drug Resistance, Neoplasm, pubmed-meshheading:9824152-Epithelial Cells, pubmed-meshheading:9824152-Female, pubmed-meshheading:9824152-Humans, pubmed-meshheading:9824152-Mice, pubmed-meshheading:9824152-Neoplasm Proteins, pubmed-meshheading:9824152-Neoplastic Stem Cells, pubmed-meshheading:9824152-Oncogenes, pubmed-meshheading:9824152-Ovarian Neoplasms, pubmed-meshheading:9824152-Ovary, pubmed-meshheading:9824152-Paclitaxel, pubmed-meshheading:9824152-Recombinant Fusion Proteins, pubmed-meshheading:9824152-Transfection, pubmed-meshheading:9824152-Tumor Cells, Cultured, pubmed-meshheading:9824152-bcl-Associated Death Protein
pubmed:year
1998
pubmed:articleTitle
BAD partly reverses paclitaxel resistance in human ovarian cancer cells.
pubmed:affiliation
Department of Adult Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't