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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
11
|
| pubmed:dateCreated |
1988-6-15
|
| pubmed:abstractText |
We investigated whether there is a relationship between the production of eicosanoids by murine solid tumors and their response to the prostaglandin H (PGH) synthase inhibitor indomethacin. Three sarcomas, designated FSA, NFSA, and SA-NH, and two carcinomas, designated MCA-K and HCA-I, syngeneic to C3Hf/Kam mice were used. In general, FSA and NFSA produced more PGH synthase products than lipoxygenase products, whereas HCA-I produced both types of metabolites in large quantities. All three tumors responded well to indomethacin treatment by slowing their growth. In contrast, MCA-K and SA-NH tumors produced insignificant quantities of PGH synthase products, but substantial amounts of lipoxygenase products. Their growth was not affected by treatment with indomethacin. Indomethacin did not influence tumor cell survival either in vitro or in vivo, but it reduced the proportion of S-phase cells in the tumors. The antitumor effect of indomethacin was not reduced by immunosuppression of the tumor host and was independent of tumor immunogenicity, implying that indomethacin acted through nonimmunological mechanisms. Thus, the effectiveness of indomethacin was directly related to the ability of tumors to produce PGs. Consequently, the eicosanoid profile of tumors could serve as a valuable way to select patients likely to respond to indomethacin and other PGH synthase inhibiting agents.
|
| pubmed:grant | |
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/6-Ketoprostaglandin F1 alpha,
http://linkedlifedata.com/resource/pubmed/chemical/Arachidonic Acid,
http://linkedlifedata.com/resource/pubmed/chemical/Arachidonic Acids,
http://linkedlifedata.com/resource/pubmed/chemical/Carbon Radioisotopes,
http://linkedlifedata.com/resource/pubmed/chemical/Indomethacin,
http://linkedlifedata.com/resource/pubmed/chemical/Prostaglandins,
http://linkedlifedata.com/resource/pubmed/chemical/Thromboxane B2,
http://linkedlifedata.com/resource/pubmed/chemical/Tritium,
http://linkedlifedata.com/resource/pubmed/chemical/Tumor Markers, Biological
|
| pubmed:status |
MEDLINE
|
| pubmed:month |
Jun
|
| pubmed:issn |
0008-5472
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:day |
1
|
| pubmed:volume |
48
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
3002-7
|
| pubmed:dateRevised |
2007-11-14
|
| pubmed:meshHeading |
pubmed-meshheading:3130182-6-Ketoprostaglandin F1 alpha,
pubmed-meshheading:3130182-Animals,
pubmed-meshheading:3130182-Arachidonic Acid,
pubmed-meshheading:3130182-Arachidonic Acids,
pubmed-meshheading:3130182-Carbon Radioisotopes,
pubmed-meshheading:3130182-Female,
pubmed-meshheading:3130182-Fibrosarcoma,
pubmed-meshheading:3130182-Indomethacin,
pubmed-meshheading:3130182-Liver Neoplasms, Experimental,
pubmed-meshheading:3130182-Male,
pubmed-meshheading:3130182-Mammary Neoplasms, Experimental,
pubmed-meshheading:3130182-Mice,
pubmed-meshheading:3130182-Mice, Inbred C3H,
pubmed-meshheading:3130182-Prognosis,
pubmed-meshheading:3130182-Prostaglandins,
pubmed-meshheading:3130182-Sarcoma, Experimental,
pubmed-meshheading:3130182-Thromboxane B2,
pubmed-meshheading:3130182-Tritium,
pubmed-meshheading:3130182-Tumor Markers, Biological
|
| pubmed:year |
1988
|
| pubmed:articleTitle |
Prostaglandin production by murine tumors as a predictor for therapeutic response to indomethacin.
|
| pubmed:affiliation |
Department of Experimental Radiotherapy, University of Texas M. D. Anderson Hospital and Tumor Institute at Houston 77030.
|
| pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
|