Suppr超能文献

补体受体 CD46、CD55 和 CD59 受头颈部癌症肿瘤微环境调控,以促进逃避补体攻击。

The complement receptors CD46, CD55 and CD59 are regulated by the tumour microenvironment of head and neck cancer to facilitate escape of complement attack.

机构信息

Department of Otorhinolaryngology and Plastic Surgery, University of Luebeck, Ratzeburger Allee 160, 23562 Luebeck, Germany; Department of Surgery, University Medical Center Regensburg, Franz-Josef-Strauß-Allee 11, 93053 Regensburg, Germany.

Department of Otorhinolaryngology and Plastic Surgery, University of Luebeck, Ratzeburger Allee 160, 23562 Luebeck, Germany; Department of Internal Medicine, University Medical Center Regensburg, Franz-Josef-Strauß-Allee 11, 93053 Regensburg, Germany.

出版信息

Eur J Cancer. 2014 Aug;50(12):2152-61. doi: 10.1016/j.ejca.2014.05.005. Epub 2014 Jun 7.

Abstract

BACKGROUND

Membrane-bound complement restriction proteins (mCRPs) CD46, CD55 and CD59 enable tumour cells to evade complement dependent cytotoxicity and antibody-dependent killing mechanisms. But less is known about the role of these mCRPs in head and neck cancer.

METHODS

In this study we determined the expression of the mCRPs on head and neck squamous cell carcinoma (HNSCC) cell lines, on tumour tissue and TDLNs (tumour-draining lymph nodes) as well as on lymphocytes from HNSCC patients. The influence of the HNSCC microenvironment on the mCRP regulation was analysed using Flow Cytometry, Western blotting and small interfering RNAs (siRNA) transfection studies.

RESULTS

We examined the effects of the HNSCC tumour milieu on the expression levels of CD46, CD55 and CD59. We investigated the susceptibility of HNSCC cells to CDC (complement-dependent cytotoxicity) while silencing the mCRPs. Our results demonstrate a huge influence of the HNSCC tumour microenvironment on the regulation of mCRP expression and show a reciprocal regulation between the different mCRPs themselves.

CONCLUSIONS

In summary, our data indicate that HNSCC has evolved different strategies to evade complement attacks and that the tumour microenvironment leads to the enhancement of complement resistance of the surrounding tissue.

摘要

背景

膜结合补体限制蛋白(mCRPs)CD46、CD55 和 CD59 使肿瘤细胞能够逃避补体依赖的细胞毒性和抗体依赖的杀伤机制。但对于这些 mCRPs 在头颈部癌症中的作用知之甚少。

方法

在这项研究中,我们确定了 mCRPs 在头颈部鳞状细胞癌(HNSCC)细胞系、肿瘤组织和 TDLNs(肿瘤引流淋巴结)以及 HNSCC 患者的淋巴细胞上的表达。使用流式细胞术、Western blot 和小干扰 RNA(siRNA)转染研究分析了 HNSCC 微环境对 mCRP 调节的影响。

结果

我们研究了 HNSCC 肿瘤环境对 CD46、CD55 和 CD59 表达水平的影响。我们研究了沉默 mCRPs 时 HNSCC 细胞对 CDC(补体依赖性细胞毒性)的敏感性。我们的结果表明 HNSCC 肿瘤微环境对 mCRP 表达的调节有巨大影响,并显示不同 mCRPs 之间存在相互调节。

结论

综上所述,我们的数据表明,HNSCC 已经进化出不同的策略来逃避补体攻击,并且肿瘤微环境导致周围组织的补体抗性增强。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验