表达活化ras癌基因的结直肠癌细胞中细胞间粘附分子1和II类组织相容性抗原的诱导

V Stoneman, A Morris
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引用次数: 2

摘要

目的:探讨ras癌基因的激活与干扰素γ (ifn - γ)诱导MHCⅱ类抗原和细胞间粘附分子1 (ICAM-1)是否存在相关性。方法:采用流式细胞术检测ⅱ类抗原、ICAM-1和细胞内ras癌蛋白(p21)在已建立的结直肠癌细胞系和短期培养的结直肠癌细胞中的表达,并通过对ras基因扩增片段的测序检测其突变。结果:HT29细胞系对MHC II类抗原和ICAM-1的表达发生了变化,从没有诱导到II类抗原表达增加98倍。先前的研究表明,大多数肿瘤不能被诱导表达II类抗原。5个最少诱导系中有4个含有突变体ras或高表达癌蛋白。四种高度诱导的细胞系均含有非突变的ras。在原代培养研究的21个肿瘤中,有10个是可诱导的,其中一个含有突变体ras。其余的非诱导肿瘤中,有4个是突变体。结论:ras激活与ifn - γ反应失败之间的相关性不能被证明是显著的。因此,ras的激活以及伴随的细胞内信号通路的破坏,可能不是II类抗原和ICAM-1无法激活的主要决定因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Induction of intercellular adhesion molecule 1 and class II histocompatibility antigens in colorectal tumour cells expressing activated ras oncogene.

Aims-To determine whether there is a correlation between activation of the ras oncogene and the induction of MHC class II antigens and intercellular adhesion molecule 1 (ICAM-1) by interferon-gamma (IFN-gamma).Methods-Expression of class II antigens, ICAM-1 and intracellular ras oncoprotein (p21) in established colorectal cell lines and short term cultures of primary colorectal tumour cells was determined by flow cytometry and mutation in the ras gene by sequencing of amplified segments of the gene.Results-The cell lines showed a variation in their modulation of MHC class II antigens and ICAM-1, ranging from no induction to a 98-fold increase in class II antigen expression in the HT29 cell line. Previous work indicated that most tumours could not be induced to express class II antigens. Four of the five least inducible lines either contained mutant ras or highly expressed the oncoprotein. The four highly inducible cell lines all contained non-mutant ras. Of the 21 tumours studied in primary culture, 10 were inducible, one of which contained mutant ras. Of the remaining non-inducible tumours, four were mutant.Conclusions-Correlations between ras activation and failure to respond to IFN-gamma could not be shown to be significant. Therefore, ras activation, and concomitant subversion of intracellular signalling pathways, is probably not the major determinant in failure to activate class II antigens and ICAM-1.

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