## Abstract Proliferation and death were measured in cultures of mouse neuroblastoma N18TGβ2 and rat glioma C6BUβ1 cells when treated with up to 100 ΞΌM retinoidal butenolides (RB 1β6). The number of viable cells in each case was measured with various concentrations of the compounds, of which RBβ3 (
Cytotoxic action of prostaglandin D2 on mouse neuroblastoma cells
β Scribed by Haruhiro Higashida; Kyoko Kano-Tanaka; Shunnosuke Natsuume-Sakai; Katsuko Sudo; Hiroko Fukami; Yuzo Nakagawa; Naomasa Miki
- Publisher
- John Wiley and Sons
- Year
- 1983
- Tongue
- French
- Weight
- 709 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0020-7136
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β¦ Synopsis
Addition to the culture medium of prostaglandin (PG) D, resulted in the degeneration in a dose-and time-dependent manner of N18TG-2 cells cloned from mouse neuroblastoma. The EDso for PGD,-induced cytotoxicity was about 10 1(~. The degenerative changes were irreversible when the cells were exposed for more than 10 h. Scanning and transmission electron microscopic examination revealed that treatment with PGD, resulted in apearance of numerous blebs of various sizes along the cell surface and also in destruction of surface membrane and of cytoplasmic organelles. Tumor weight of N 18TG-2 neuroblastoma inoculated subcutaneously on the backs of A/J mice was about 35-70 YO less than that of controls after 14 days of single daily i.p. or S.C. injections of 0.5-1 mg/kg of PGD,. The results indicate that PGD, has growth-inhibitory effects on mouse neuroblastoma cells in vitro and in vivo.
π SIMILAR VOLUMES
We investigated the effects of vitamin D3 on the signaling pathways by prostaglandin E, (PGE2) in osteoblast-like MC3T3-El cells. The pretreatment with 1,25-dihydroxyvitamin D3 (1 ,25-(OH),D3), an active form of vitamin D3, significantly inhibited cAMP accumulation induced by 10 (LM PGE, in a dose-d