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Learning tasks as a possible treatment for DNA lesions induced by oxidative stress in hippocampal neurons 被引量:7
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作者 Dragos Cīrneci Radu Silaghi-Dumitrescu 《Neural Regeneration Research》 SCIE CAS CSCD 2013年第32期3063-3070,共8页
Reactive oxygen species have been implicated in conditions ranging from cardiovascular dysfunc- tion, arthritis, cancer, to aging and age-related disorders. The organism developed several path- ways to counteract thes... Reactive oxygen species have been implicated in conditions ranging from cardiovascular dysfunc- tion, arthritis, cancer, to aging and age-related disorders. The organism developed several path- ways to counteract these effects, with base excision repair being responsible for repairing one of the major base lesions (8-oxoG) in all organisms. Epidemiological evidence suggests that cognitive stimulation makes the brain more resilient to damage or degeneration. Recent studies have linked enriched environment to reduction of oxidative stressin neurons of mice with Alzheimer's dis- ease-like disease, but given its complexity it is not clear what specific aspect of enriched environ- ment has therapeutic effects. Studies from molecular biology have shown that the protein p300, which is a transcription co-activator required for consolidation of memories during specific learning tasks, is at the same time involved in DNA replication and repair, playing a central role in the long-patch pathway of base excision repair. Based on the evidence, we propose that learning tasks such as novel object recognition could be tested as possible methods of base excision repair fa- cilitation, hence inducing DNA repair in the hippocampal neurons. If this method proves to be effec- tive, it could be the start for designing similar tasks for humans, as a behavioral therapeutic com- plement to the classical drug-based therapy in treating neurodegenerative disorders. 展开更多
关键词 neural regeneration REVIEWS neurodegenerative disorder reactive oxygen species base excisionrepair cognitive stimulation P300 grants-supported paper neural regeneration
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乳腺癌石蜡肿瘤组织和相应血液细胞BRCA1、ERCC1、TS mRNA的表达相关性研究 被引量:1
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作者 王露 孙怡 +1 位作者 李惠 王剑蓉 《中国当代医药》 2014年第27期7-10,15,共5页
目的探讨乳腺癌石蜡肿瘤组织和相应血液细胞中乳腺癌易感基因1(BRCA1)与切除修复交叉互补基因1(ERCC1)及胸苷酸合成酶(TS)基因表达的相关性,同时探讨BRCA1、ERCC1、TS在乳腺癌肿瘤组织与对应患者血液细胞中表达的关系。方法收集53例乳... 目的探讨乳腺癌石蜡肿瘤组织和相应血液细胞中乳腺癌易感基因1(BRCA1)与切除修复交叉互补基因1(ERCC1)及胸苷酸合成酶(TS)基因表达的相关性,同时探讨BRCA1、ERCC1、TS在乳腺癌肿瘤组织与对应患者血液细胞中表达的关系。方法收集53例乳腺癌肿瘤石蜡标本及其对应的血液样本,利用实时荧光定量PCR技术检测肿瘤石蜡组织和对应血液样本中BRCA1、ERCC1、TS mRNA的表达水平;利用Pearson相关性分析方法分析肿瘤石蜡组织和相应血液细胞BRCA1、ERCC1、TS mRNA表达的相关性以及肿瘤石蜡组织细胞BRCA1、ERCC1、TS mRNA之间表达的相关性。结果乳腺癌石蜡组织中BRCA1 mRNA表达的ΔCT为(7.516±2.257),对应的血液组织中为(10.374±2.519)。乳腺癌石蜡组织中ERCC1和TS mRNA表达的ΔCT分别为(6.114±2.944)、(5.950±2.604),对应的血液组织分别为(8.801±2.581)、(10.078±1.731)。Pearson相关性分析显示,BRCA1、ERCC1在肿瘤石蜡组织与血液组织中的表达均呈正相关(r=0.607、0.537,P<0.05)。肿瘤石蜡组织与血液组织中的TS表达无相关性(r=0.074,P>0.05)。BRCA1与ERCC1在肿瘤石蜡组织中的表达无相关性(r=0.250,P>0.05)。BRCA1与TS在肿瘤石蜡组织中的表达无相关性(r=0.256,P>0.05)。ERCC1与TS在肿瘤石蜡组织中的表达无相关性(r=0.169,P>0.05)。结论乳腺癌患者的血液标本也许可以替代其肿瘤石蜡组织检测BRCA1和ERCC1 mRNA的表达;BRCA1与ERCC1、TS的表达无相关性。 展开更多
关键词 乳腺癌 乳腺癌易感基因1 切除修复交叉互补基因1 胸苷酸合成酶基因
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