Tímár J, Ladányi A, Lapis K, Moczar E
First Institute of Pathology and Experimental Cancer Research, Semmelweis Medical University, Budapest, Hungary.
J Cancer Res Clin Oncol. 1990;116(3):264-70. doi: 10.1007/BF01612901.
Biochemical and cytochemical analysis of Lewis lung tumor variants revealed that the low metastatic cells contained more galactose/N-acetylgalactosamine residues in a high-molecular-mass (15-20 kDa) mixed N- and O-glycan fraction than the highly metastatic ones. It was also found that the highly metastatic variant was less sensitive to macrophage cytotoxicity in vitro. The cytotoxicity against the low metastatic target cells was inhibited by asialofetuin (10-20 microM), and, to a small degree--and at much higher concentration--by lactose, while galactose and other monosaccharides were ineffective. We suppose that complex galactosylated tumor cell membrane glycans could play a role in the antitumoral cytotoxicity of macrophages.
对Lewis肺癌变体进行的生化和细胞化学分析显示,低转移细胞在高分子量(15 - 20 kDa)的混合N - 聚糖和O - 聚糖组分中比高转移细胞含有更多的半乳糖/N - 乙酰半乳糖胺残基。还发现高转移变体在体外对巨噬细胞细胞毒性的敏感性较低。去唾液酸胎球蛋白(10 - 20 microM)可抑制对低转移靶细胞的细胞毒性,乳糖在较小程度上且在高得多的浓度下也有抑制作用,而半乳糖和其他单糖则无作用。我们推测复杂的半乳糖基化肿瘤细胞膜聚糖可能在巨噬细胞的抗肿瘤细胞毒性中发挥作用。