首页> 外文期刊>Human Immunology: Official Journal of the American Society for Histocompatibility and Immunogenetics >Peroxynitrite modified DNA may be an antigenic trigger for antibodies in various cancers of gynecologic origin
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Peroxynitrite modified DNA may be an antigenic trigger for antibodies in various cancers of gynecologic origin

机译:过氧基酯改性DNA可以是抗原触发用于妇科来源的各种癌症中的抗体

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This study aimed towards probing the role of peroxynitrite damaged human DNA (ONOO--DNA) in the induction of circulating antibodies in certain cancers of gynecologic origin. We have compared the binding specificity of DNA isolated from the lymphocytes of cancer patients with that of the experimentally modified DNA. Also, the induced anti-ONOO--DNA antibodies have been used to probe oxidative damage in the DNA isolated from cancer patients. Human placental DNA was modified with peroxynitrite (ONOO-) and analyzed by ultraviolet (UV) and fluorescence spectroscopy, gel electrophoresis, thermal denaturation profile, etc. Antibodies against modified DNA were induced in experimental animals. Specific binding of the antibodies was evaluated by ELISA and band shift assay. 91 cancer patients were selected and grouped according to the type of cancer. Specific binding characteristics of circulating autoantibodies (IgG) were determined by competitive-inhibition ELISA, using different inhibitors. Maximum inhibition of antibody activity by ONOO--DNA reflected specific recognition of modified epitopes by cancer IgG. This shows generation of neo-epitopes on DNA, upon modification with ONOO-, that are recognized by cancer IgG. Our results indicate epitope sharing between the DNA isolated from cancer patients and the in-vitro modified ONOO--DNA. The possible role of nitrosative stress in the gynecologic oncology has been discussed.
机译:本研究旨在探讨过氧硝酸盐受损人DNA(ONOO - DNA)在妇科来源的某些癌症中循环抗体诱导中的作用。我们已经比较了从癌症患者淋巴细胞中分离的DNA的结合特异性,具有实验修饰的DNA的淋巴细胞。此外,诱导的抗onOO - DNA抗体已用于探测癌症患者分离的DNA中的氧化损伤。用过氧基硝酸盐(ONOO-)改性人的胎盘DNA,并通过紫外(UV)和荧光光谱,凝胶电泳,热变性谱等进行分析,在实验动物中诱导针对改性DNA的抗体。通过ELISA和带移测定评估抗体的特异性结合。根据癌症的类型选择并分组91例癌症患者。使用不同抑制剂的竞争抑制ELISA测定循环自身抗体(IgG)的特异性结合特征。 ONOO - DNA对抗体活性的最大抑制反映了癌症IgG修饰表位的特异性识别。这表明,在用癌症IgG识别的onoo-onoOO-后,在DNA上产生Neo-epitopes的产生。我们的结果表明,从癌症患者和体外改性的ONOO-DNA分离的DNA之间的表位分担。讨论了亚硝酸盐胁迫在妇科肿瘤中的可能作用。

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