1-palmitoyl-2-linoleoyl-3-acetyl-rac-glycerol and Biliary-Tract-Neoplasms

1-palmitoyl-2-linoleoyl-3-acetyl-rac-glycerol has been researched along with Biliary-Tract-Neoplasms* in 1 studies

Other Studies

1 other study(ies) available for 1-palmitoyl-2-linoleoyl-3-acetyl-rac-glycerol and Biliary-Tract-Neoplasms

ArticleYear
EC-18, a synthetic monoacetyldiacylglyceride, inhibits hematogenous metastasis of KIGB-5 biliary cancer cell in hamster model.
    Journal of Korean medical science, 2009, Volume: 24, Issue:3

    EC-18 (monoacetyldiacylglyceride) stimulates T cell production of IL-2, IL-4, IL-12, IFN-gamma, and GM-CSF in vitro. To study the effects of these cytokines stimulated by EC-18 on cancer cells, we applied hamster biliary cancer model, a difficult cancer to treat. Cancer (KIGB-5) cells were given intravenously to produce hematogenous metastatic lung lesions which were treated with EC-18 at 10, 25, and 50 mg/kg/day respectively. The fourth group was untreated control. At 4th, 8th, and 12th week the lungs were examined. EC-18 treated groups showed only a few microscopic lung lesions and no evidence of metastatic lesion with highest dose whereas widespread gross lung lesions were observed in untreated control. To investigate whether the anti-tumor effect of EC-18 is associated with suppression of tumor cell Toll-like receptor 4 (TLR-4) expression in addition to stimulation of the immune cells, KIGB-5 cells were exposed to LPS with or without EC-18. TLR-4 mRNA and protein expression, measured by reverse transcriptase PCR (RT-PCR), real-time quantitative PCR and western blot analysis, showed suppression of TLR-4 expression in KIGB-5 cells treated with EC-18 compared with control. In conclusion, EC-18 has a significant anti-tumor effect in this experimental model of biliary cancer suggesting potential for clinical application to this difficult cancer.

    Topics: Animals; Antineoplastic Agents; Biliary Tract Neoplasms; Cricetinae; Cytokines; Diglycerides; Female; Glycerides; Lung; Neoplasm Metastasis; T-Lymphocytes; Toll-Like Receptor 4; Tumor Cells, Cultured

2009