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化学诱导的BALB/c Meth A肉瘤中分子量为110,000的肿瘤排斥抗原的特性

Properties of a M(r) 110,000 tumor rejection antigen of the chemically induced BALB/c Meth A sarcoma.

作者信息

De Leo A B, Becker M, Lu L, Law L W

机构信息

Pittsburgh Cancer Institute, Division of Basic Research, Pennsylvania 15213.

出版信息

Cancer Res. 1993 Apr 1;53(7):1602-7.

PMID:7680955
Abstract

A M(r) 110,000 glycoprotein, designated gp110, isolated from the concanavalin A-Sepharose-binding protein fraction of the chemically induced BALB/c Meth A sarcoma by Mono Q fast protein liquid chromatography, has been shown to: (a) increase the resistance of these mice to growth of the Meth A sarcoma, but not the antigenically unrelated BALB/c CI-4 sarcoma, and (b) induce an antitumor cellular immune response in mice, which was detectable in cell-mediated cytotoxic assays. The immunogenicity of the concanavalin A-Sepharose-binding protein fraction of Meth A cytosol had been attributed to gp96, the major component of this fraction. The evidence presented here, however, demonstrates that Meth A gp96, when sufficiently purified, is nonimmunogenic. The results of the present analysis of gp110 strongly support the concept that gp110 represents a family of proteins expressed on a variety of chemically induced tumors, in which variations in molecular fine structure account for the antigenic diversity associated with these tumors.

摘要

通过Mono Q快速蛋白质液相色谱法从化学诱导的BALB/c Meth A肉瘤的伴刀豆球蛋白A-琼脂糖结合蛋白组分中分离出一种分子量为110,000的糖蛋白,命名为gp110,它已被证明:(a) 可增强这些小鼠对Meth A肉瘤生长的抵抗力,但对抗原性无关的BALB/c CI-4肉瘤无效;(b) 在小鼠中诱导抗肿瘤细胞免疫反应,这在细胞介导的细胞毒性试验中可检测到。Meth A细胞溶质的伴刀豆球蛋白A-琼脂糖结合蛋白组分的免疫原性曾被认为归因于该组分的主要成分gp96。然而,此处提供的证据表明,充分纯化后的Meth A gp96无免疫原性。对gp110的当前分析结果有力支持了这一概念,即gp110代表一类在多种化学诱导肿瘤上表达的蛋白质家族,其中分子精细结构的变化解释了与这些肿瘤相关的抗原多样性。

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