We established gastric cancer-specific CD8 1 T-cell (T CD8 1) lines derived from different lymphocyte sources in the same patients by repeated stimulation with mitomycin-C-treated autologous tumor cells with low-dose interleukin-2, and we compared recognition patterns among the T CD8 1 derived from
Induction of the fundic mucosa-specific glycolipid with dimethylformamide in gastric-cancer cell lines
β Scribed by Taeko Dohi; Miyuki Nakasuji; Mieko Oshima
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- French
- Weight
- 460 KB
- Volume
- 53
- Category
- Article
- ISSN
- 0020-7136
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β¦ Synopsis
We have previously reported that a glycolipid GalNAcp I -4[NeuAcc~2-3]Galp I -4GlcNAcp I -3Galp I -4Glc-Cer named NGM-I is present specifically in the human gastric fundic mucosa, but not in other organs. In gastric-cancer tissue and cancer cell lines, this glycolipid completely disappears. These findings imply that NGM-I is expressed only in well-differentiated fundic mucosa. The purpose of this study is to examine the expression of NGM-I as a differentiation-related molecule. A gastric cell line AZ52 I was cultured in the medium with various reagents which had been reported to induce differentiation in cancer cells. The growth of AZ52I was suppressed by the addition of 0.8% dimethylformamide (DMF) to the medium, but not by addition of dimethylsulfoxide (DMSO), retinoic acid or butyric acid. In the ganglioside fraction of the cells cultured with DMF. a glycolipid regarded as NGM-I which had not been present before treatment was detected using a monoclonal antibody. Suppression of the proliferation of AZ52 I by eliminating the serum from the medium could not induce the expression of NGM-I. A colonic cell line treated with DMF also failed to express the glycolipid. The synthase activity of NGM-I was elevated in the AZ52I cells treated with DMF, but not with DMSO. These results demonstrate that the expression of NGM-I is induced by DMF specifically in gastric-cancer cells, and suggest the possibility that NGM-I is a differentiationrelated molecule.
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