Diagnostics R&D Department, Asahi Chemical Industry Co., Ltd., Ohito-cho, Shizuoka, 410-2321, Japan,
Cytotechnology. 1999 Nov;31(3):255-63. doi: 10.1023/A:1008061424281.
The expression of glycosylphosphatidylinositol (GPI-anchored) carcinoembryonic antigen (CEA) and alkaline phosphatase (ALP) on the cell surface of various cancer cell lines and a lung diploid cell line (WI38) was investigated, with exposure of the cell lines to a cell differentiation agent (sodium butyrate) to induce cell differentiation and expression of the two tumor-associated antigens. In three colon (SW1222, SW1116, and HT-29) and stomach (MKN-45) cancer cell lines, all of which are double producers of CEA and ALP, the maximum expression of GPI-anchored CEA occurred with butyrate at a lower concentration than did that of GPI-anchored ALP. GPI-anchored ALP derived from colon (SW1222 and SW1116) and stomach (MKN-45 and MKN-1) cancer cell lines was heat-stable with and without exposure to butyrate, but GPI-anchored ALP derived from lung cancer cell lines (PC-6, PC13, PC-14, WI26VA4, and WI38VA13) showed a variety of heat stabilities, depending on cell line, butyrate exposure, and SV40 transformation.
研究了糖基磷脂酰肌醇(GPI)锚定癌胚抗原(CEA)和碱性磷酸酶(ALP)在各种癌细胞系和肺二倍体细胞系(WI38)表面的表达情况,并通过细胞分化剂(丁酸钠)暴露于细胞系,以诱导细胞分化和两种肿瘤相关抗原的表达。在三种结肠(SW1222、SW1116 和 HT-29)和胃(MKN-45)癌细胞系中,CEA 和 ALP 均为双产物,GPI 锚定 CEA 的最大表达发生在较低浓度的丁酸钠下,而 GPI 锚定 ALP 的表达则较低。来自结肠(SW1222 和 SW1116)和胃(MKN-45 和 MKN-1)癌细胞系的 GPI 锚定 ALP 在有或没有丁酸钠暴露的情况下均具有热稳定性,但来自肺癌细胞系(PC-6、PC13、PC-14、WI26VA4 和 WI38VA13)的 GPI 锚定 ALP 表现出多种热稳定性,这取决于细胞系、丁酸钠暴露和 SV40 转化。