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国家自然科学基金(81072220)

作品数:3 被引量:4H指数:1
相关作者:孙仑泉陶永光曹亚杨力芳卢景琛更多>>
相关机构:中南大学卫生部更多>>
发文基金:国家自然科学基金国家高技术研究发展计划更多>>
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Use of DNAzymes for cancer research and therapy被引量:3
2012年
DNAzymes(Dzs) are single-stranded DNA catalysts that specifically cleave the mRNA of targeted genes.Compared with other gene-silencing technologies,such as ribozymes,antisense oligonucleotide and small interference RNA(siRNA),DNAzymes have several advantages,including small molecular weight,diversity,low cost and relative stability in serum.With the evolution of molecular technology,the first DNAzyme was generated in vitro in 1994.From then on,DNAzymes have been studied in order to understand their structures,chemistry and biological applications.Particularly,DNAzymes have been widely applied as a new interference strategy in the treatment of many conditions,including cancer,viral diseases,and cardiovascular diseases.This review mainly summarizes the use of DNAzymes in the areas of cancer research and therapy.
XU ZhiJieYANG LiFangSUN LunQuanCAO Ya
关键词:脱氧核酶小干扰RNA分子生物技术病毒性传染病
Role of epidermal growth factor receptor in DNA damage repair被引量:1
2011年
Many human tumor cells are characterized by overexpression or mutation of epidermal growth factor receptor (EGFR). Emerging evidence indicates that EGFR, as well as some of its downstream components, can translocate to the nucleus and play roles in transcriptional regulation, signaling conduction and repair of DNA double strands breaks (DSBs). EGFR in its nuclear manifestation promotes DSB repair by interacting with proteins including DNA-PK, ATM, Rad51 and BRCA1, involved in DSB repair, via the PI3K-Akt and Ras-Raf-MAPK pathways. DNA damage repair in tumor cells is emerging as an attractive target in radiotherapy and chemotherapy. Interruption of EGFR functions, or those of its downstream components, presents a promising strategy for confounding DNA damage repair in tumor cells.
LU JingChenYANG LiFangTAO YongGuangSUN LunQuanCAO Ya
关键词:表皮生长因子受体DNA损伤修复MAPK途径双链断裂自动柜员机BRCA1
表皮生长因子受体在DNA损伤修复中的作用机制新进展
2011年
表皮生长因子受体(epidermal growth factor receptor,EGFR)在许多人类恶性肿瘤中存在过表达或突变,近期大量的研究表明EGFR和/或其下游成分可以进入细胞核,在核内发挥转录调节和信号转导功能,其中一个重要的功能是促进DNA双链断裂(double strands breaks,DSBs)的修复.EGFR主要通过核移位及PI3K-Akt通路、Ras-Raf-MAPK通路与DNA修复的关键成分如DNA-PK,ATM,Rad51和BRCA1等作用促进DSBs的修复.放化疗诱导的肿瘤细胞DNA损伤后的修复目前正成为一个越来越有吸引力的靶点,靶向EGFR或其下游信号抑制DNA损伤修复的治疗具有重要的临床意义和应用前景.
卢景琛杨力芳陶永光孙仑泉曹亚
关键词:表皮生长因子受体核移位电离辐射DNA损伤修复
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