journal article·2013-04-10

Real Time in Vitro Regulation of DNA Methylation Using a 5-Fluorouracil Conjugated DNA-Based Stimuli-Responsive Platform

Xiuhai Mao, Ming Wei, Chengfeng Zhu, Jianxin Lu, Jimin Gao, Anna J. Simon, Jiye Shi, Qing Huang, Chunhai Fan

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Abstract

DNA methylation, catalyzed by methylases, plays a critical role in many biological processes, and many methylases have been regarded as promising targets for antimicrobial drugs. In this work, we report a stimulus responsive, self-regulating anticancer drug release platform, comprising a multifunctional DNA that upon methylation by methyltransferase (MTase) releases 5-fluorouracil (5-Fu) and in turn inhibits subsequent expression of MTase. The multifunctional DNA with anticancer drug are first methylated by DNA adenine methylation (DAM) methyltransferase (MTase) and then cut by the methylation-sensitive restriction endonuclease Dpn I. Removal of duplex from the functional DNA by the methylation/cleavage process will release the anticancer drug, resulting in inhibition of the activity of DAM in turn. Consequently, the enzyme activity of DAM MTase can be self-regulated. Furthermore, we found that the inhibition efficiency of 5-Fu significantly increase as it is functionalized with DNA.
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Research context

OpenAlex topics: Epigenetics and DNA Methylation · Advanced biosensing and bioanalysis techniques · Genetics and Neurodevelopmental Disorders

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Laboratory of Physical Biology, Shanghai Institute of Applied Physics, Chinese Academy of Sciences, Shanghai, China

Key Laboratory of Laboratory Medicine, Ministry of Education, Wenzhou Medical College, Wenzhou 325035, Zhejiang, China

Department of Chemistry, and Biomolecular Science and Engineering Program, University of California, Santa Barbara, California 93106, United States

UCB Pharma, 208 Bath Road, Slough SL1 3WE, United Kingdom

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