Source:http://linkedlifedata.com/resource/pubmed/id/11596291
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
9
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pubmed:dateCreated |
2001-10-12
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pubmed:abstractText |
McAb 3A5, a rat monoclonal antibody, was linked to pingyangmycin (PYM), an antitumor antibiotic identical to bleomycin A5 currently in clinical use, employing Dextran T-40 as an intermediate agent. The 3A5-PYM conjugate retained complete immunoreactivity of McAb 3A5. Determined by clonogenic assay with colon cancer HT-29 cells, the IC50 values for 3A5-PYM conjugate and free PYM were 0.6 mumol.L-1 and 10.2 mumol.L-1, respectively. Hepatoma H22 ascites was transplanted into the peritoneal or thoracic cavity of mice. On the next day, 3A5-PYM or PYM, were injected into the cavity. Therapeutic effect was evaluated on the survival time of mice. For intraperitoneal tumor, the ILS(%) values were 238% for 3A5-PYM and 40% for PYM. For intrapleural tumor, the ILS(%) values were 384% for 3A5-PYM and 66% for PYM. Murine hepatoma H22 was transplanted s.c. into mice and 3A5-PYM conjugate or free PYM were injected peritumorally. As determined by antimicrobial assay, the administration of 3A5-PYM showed higher concentration and longer retention time in the tumor than that of free PYM. Tumor fragments of human colon cancer HT-29 were transplanted s.c. into nude mice. Then 3A5-PYM or PYM was injected i.v., i.p. or pt (peritumorally) 3 days after inoculation, twice a week, with a total of 7 injections. Tumor growth inhibition was evaluated 4 weeks later. The inhibition rates on the growth of colon cancer xenografts were as follows: (1) for i.v. route, 58% by PYM, 79% by 3A5-PYM; (2) for i.p. route, 52% by PYM, 61% by 3A5-PYM; and (3) for pt route, 73% by PYM, 96% by 3A5-PYM. These results indicate that 3A5-PYM conjugate is highly effective against targeted human cancer xenograft and mouse tumor when administered peritumorlly or intracavitarily.
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pubmed:language |
chi
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antibiotics, Antineoplastic,
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Monoclonal,
http://linkedlifedata.com/resource/pubmed/chemical/Bleomycin,
http://linkedlifedata.com/resource/pubmed/chemical/Immunotoxins,
http://linkedlifedata.com/resource/pubmed/chemical/zhengguangmycin
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0513-4870
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
32
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
669-74
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:11596291-Animals,
pubmed-meshheading:11596291-Antibiotics, Antineoplastic,
pubmed-meshheading:11596291-Antibodies, Monoclonal,
pubmed-meshheading:11596291-Bleomycin,
pubmed-meshheading:11596291-Female,
pubmed-meshheading:11596291-HT29 Cells,
pubmed-meshheading:11596291-Humans,
pubmed-meshheading:11596291-Immunotoxins,
pubmed-meshheading:11596291-Liver Neoplasms, Experimental,
pubmed-meshheading:11596291-Male,
pubmed-meshheading:11596291-Mice,
pubmed-meshheading:11596291-Mice, Inbred BALB C,
pubmed-meshheading:11596291-Mice, Nude,
pubmed-meshheading:11596291-Tumor Cells, Cultured
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pubmed:year |
1997
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pubmed:articleTitle |
[Use of monoclonal antibody-pinyangmycin conjugate in experimental regional targeting therapy of tumor].
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pubmed:affiliation |
Institude of Medicinal Biotechnology, Chinese Academy of Medical Science and Peking Union Medical College, Beijing 100050.
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pubmed:publicationType |
Journal Article,
English Abstract,
Research Support, Non-U.S. Gov't
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