期刊文献+

RNA干扰与高内涵筛选联合应用于药物研发的前景及其挑战 被引量:1

Prospects and challenges of applying RNAi combined with high content screening in drug development
原文传递
导出
摘要 RNAi与高内涵筛选联合应用,可作为药物研发过程中大规模靶标筛选、候选靶标确证的重要方法,还可用于化合物的筛选及作用机制研究;在HCS技术平台上平行进行功能基因组学和化学遗传学研究可同时筛选靶标和先导化合物。RNAi与HCS联合应用在药物研发中显示显著优势的同时,也常被数据的捕获、管理、分析等技术挑战所限制,尤其是海量图像的自动分析,如细胞分界及细胞表型识别分类等。 Combination of RNAi with high content screening (HCS) provides a powerful tool to carry out large-scale screens to discover and validate drug targets. It is also very useful in compound screening and mechanism research. Parallel use of chemical genetic approach and genome-wide RNAi screening on HCS platform can facilitate identifying drug targets and discovering leading compounds at the same time. The application of RNAi combined with HCS shows significant advantages in drug development. However, it is still often limited by technical challenges in the processes of acquisition, management and analysis of data, particularly in automatic analysis for massive images, such as cellular segmentation and cellular phenotype classification.
作者 杨亚平 李敏
出处 《中国新药杂志》 CAS CSCD 北大核心 2009年第8期681-685,共5页 Chinese Journal of New Drugs
关键词 RNA干扰 高内涵筛选 靶标筛选 化合物筛选 图像分析 RNAi high content screening target identification compound screening image analysis
  • 相关文献

参考文献30

  • 1JOHN M, CONSTIEN R, AKINC A, et al. Effective RNAi-mediated gene silencing without interruption of the endogenous microRNA pathway [ J ]. Nature, 2007,449 ( 7163 ) :745 - 747. 被引量:1
  • 2COUZIN J. Breakthrough of the year. Small RNAs make big splash [ J ]. Science, 2002,298 (5602) : 2296 - 2297. 被引量:1
  • 3DENNIS C. Small RNAs: The genome's guiding hand? [J]. Nature, 2002,420(6917) :732. 被引量:1
  • 4SACHSE C, KRAUSZ E, KRONKE A, et al. High-throughput RNA interference strategies for target discovery and validation by using synthetic short interfering RNAs: functional genomics investigations of biological pathways[ J]. Methods Enzymol, 2005, 392: 242 - 277. 被引量:1
  • 5HANEY SA. RNAi and high-content screening in target identification and validation[J]. IDrugs, 2005,8(12) : 997 -1001. 被引量:1
  • 6BARTZ S, JACKSON AL. How will RNAi facilitate drug development? [J]. Sci STKE, 2005,295 :pe39. 被引量:1
  • 7GIULIANO KA, DEBIASIO RL, DUNLAY RT, et al. High-content screening : a new approach to easing key bottlenecks in the drug discovery process[J]. J Biomol Screen, 1997,2(4) :249 -259. 被引量:1
  • 8GIULIANO KA, HASKINS JR, TAYLOR DL. Advances in high content screening for drug discovery[J]. Assay Drug Dev Technol, 2003,1 (4) :565 -577. 被引量:1
  • 9ABRAHAM VC, TAYLOR DL, HASKINS JR. High content screening applied to large-scale biology [J]. Trends Biotechnol, 2004,22(1) :15 -22. 被引量:1
  • 10RAUSCH O. Use of high-content analysis for compound screening and target selection [J]. IDrugs, 2005,8 (7) :573 - 577. 被引量:1

同被引文献7

  • 1Sioud M. Promises and challenges in developing RNAi as a research tool and therapy[J]. Methods Mol Biol, 2011, 703: 173-187. 被引量:1
  • 2Pardridge WM. shRNA and siRNA delivery to the brain[J]. Adv Drug DelivRev, 2007, 59(2-3): 141-152. 被引量:1
  • 3Fletcher B S. Delivery of small interfering RNA (siRNA) using the sleeping beauty transposon[J]. Cold Spring Harb Protoc, 2010, (11): 5521. 被引量:1
  • 4Van Mil A, Doevendans P A, Sluijter J P. The potential of modulating small RNA activity in vivo[J]. Mini Rev Med Chem, 2009, 9(2): 235-248. 被引量:1
  • 5Ryter S W, Alam J, Choi A M. Heme oxygenase-1/carbon monoxide: from basic science to therapeutic applications[J]. Physiol Rev, 2006, 86(2): 583-650. 被引量:1
  • 6Syapin P J. Regulation of haeme oxygenase-1 for treatment of neuroinflammation and brain disorders[J]. Br J Pharmacol, 2008, 155(5): 623 -640. 被引量:1
  • 7周红建,黄松,王雄伟.RNAi技术研究新进展[J].生物技术通报,2010,26(12):84-87. 被引量:8

引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部