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补体抑制剂信使核糖核酸在人体组织和肿瘤中的表达。

Expression of messenger RNAs for complement inhibitors in human tissues and tumors.

作者信息

Kumar S, Vinci J M, Pytel B A, Baglioni C

机构信息

Department of Biological Sciences, State University of New York, Albany 12222.

出版信息

Cancer Res. 1993 Jan 15;53(2):348-53.

PMID:7678074
Abstract

The mRNAs coding for three complement inhibitors produced by human cells, complement cytolysis inhibitor (CLI), decay-accelerating factor (DAF), and CD59, are characteristically distributed among normal tissues. High levels of CLI mRNA are expressed in tissues that express low levels of DAF mRNA and vice versa. Therefore, the expression of these mRNAs shows a mutually exclusive relationship, with the possible exception of the lung, where all these mRNAs are expressed. In contrast, CD59 mRNA is rather uniformly expressed in all tumor cell lines examined, whereas the mRNA for either of the two other complement inhibitors is overexpressed in some specific tumor cells, e.g., HeLa cells overexpress DAF mRNA, while A172 cells overexpress CLI mRNA. These two cell lines were resistant to antibody-dependent complement cytotoxicity. Expression of CLI and DAF mRNA was induced in cells treated with the antitumor drug N-(chloroetyl)-N'-cyclohexyl-N-nitrosourea; these cells became resistant to complement cytotoxicity. A similar pattern of expression was detected in tumor samples obtained during surgery, with a relatively uniform expression of CD59 mRNA and occasional overexpression of CLI or DAF mRNA. These findings suggest that overexpression of complement inhibitors mRNA and of the corresponding proteins may contribute to tumor cell resistance to complement-mediated cytotoxicity.

摘要

人类细胞产生的三种补体抑制剂(补体细胞溶解抑制剂(CLI)、衰变加速因子(DAF)和CD59)的编码mRNA在正常组织中有特征性分布。CLI mRNA在表达低水平DAF mRNA的组织中高表达,反之亦然。因此,这些mRNA的表达呈现相互排斥的关系,但肺可能是个例外,在肺中所有这些mRNA均有表达。相比之下,CD59 mRNA在所有检测的肿瘤细胞系中表达较为均匀,而另外两种补体抑制剂中任何一种的mRNA在某些特定肿瘤细胞中过表达,例如,HeLa细胞过表达DAF mRNA,而A172细胞过表达CLI mRNA。这两种细胞系对抗体依赖性补体细胞毒性具有抗性。用抗肿瘤药物N-(氯乙基)-N'-环己基-N-亚硝基脲处理的细胞中诱导了CLI和DAF mRNA的表达;这些细胞对补体细胞毒性产生了抗性。在手术期间获取的肿瘤样本中检测到类似的表达模式,CD59 mRNA表达相对均匀,偶尔有CLI或DAF mRNA的过表达。这些发现表明补体抑制剂mRNA及相应蛋白质的过表达可能有助于肿瘤细胞抵抗补体介导的细胞毒性。

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