Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2-3
|
pubmed:dateCreated |
1989-11-7
|
pubmed:abstractText |
BMY-28090 is a novel actinomycete fermentation derived antitumor agent. The cytotoxic effect of BMY-28090 was evaluated in two murine and eight human tumor cell lines in vitro. Following 72-hour exposures, BMY-28090 was cytotoxic for all of these cell lines with IC50 values of less than 0.02 to 3.25 micrograms/ml. BMY-28090 was evaluated for in vivo antitumor activity in a variety of experimental murine tumor and human tumor xenograft models. Initial testing against the murine tumor models was performed using BMY-28090 as the water insoluble free base whereas subsequent antitumor tests were performed using water soluble lactate or succinate salts. BMY-28090 administered ip demonstrated good, reproducible antitumor activity against ip implanted P388 leukemia, L1210 leukemia, B16 melanoma and M5076 sarcoma. The water soluble preparations of BMY-28090 were active iv against sc implanted B16 melanoma and M5076 sarcoma as well as subrenal capsule (src) M5076 sarcoma; activity against src implanted B16 was marginal. BMY-28090 lactate was also evaluated for activity against src implanted MX-1 human mammary tumor xenografts in nude mice and the HCT116 human colon tumor xenografts in immune-suppressed BDF1 mice. At maximum tolerated doses administered ip, BMY-28090 was active against the MX-1 xenograft in two of three tests, causing greater than 90% inhibition of tumor growth. BMY-28090 administered iv at maximally tolerated doses had marginal activity against the HCT116 xenografts, producing 61% and 68% inhibition of tumor growth in two tests. The results of these studies demonstrated that BMY-28090 has a broad spectrum of in vitro cytotoxicity against both murine and human tumor cell lines.(ABSTRACT TRUNCATED AT 250 WORDS)
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Jul
|
pubmed:issn |
0167-6997
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
7
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
173-8
|
pubmed:dateRevised |
2004-11-17
|
pubmed:meshHeading |
pubmed-meshheading:2793369-Aminoglycosides,
pubmed-meshheading:2793369-Animals,
pubmed-meshheading:2793369-Anti-Bacterial Agents,
pubmed-meshheading:2793369-Antibiotics, Antineoplastic,
pubmed-meshheading:2793369-Cell Survival,
pubmed-meshheading:2793369-Leukemia L1210,
pubmed-meshheading:2793369-Leukemia P388,
pubmed-meshheading:2793369-Mice,
pubmed-meshheading:2793369-Mice, Inbred BALB C,
pubmed-meshheading:2793369-Mice, Inbred C57BL,
pubmed-meshheading:2793369-Mice, Inbred DBA,
pubmed-meshheading:2793369-Mice, Nude,
pubmed-meshheading:2793369-Tumor Cells, Cultured
|
pubmed:year |
1989
|
pubmed:articleTitle |
Experimental antitumor activity of BMY-28090, a new antitumor antibiotic.
|
pubmed:affiliation |
Bristol-Myers Co., Inc., Pharmaceutical Research and Development Division, Wallingford, CT 06492.
|
pubmed:publicationType |
Journal Article
|