18
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      DNA methylation in development and human disease.

      1 , ,
      Mutation research
      Elsevier BV

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          DNA methylation is a heritable and stable epigenetic mark associated with transcriptional repression. Changes in the patterns and levels of global and regional DNA methylation regulate development and contribute directly to disease states such as cancer. Recent findings provide intriguing insights into the epigenetic crosstalk between DNA methylation, histone modifications, and small interfering RNAs in the control of cell development and carcinogenesis. In this review, we summarize the recent studies in DNA methylation primarily focusing on the interplay between different epigenetic modifications and their potential role in gene silencing in development and disease. Although the molecular mechanisms involved in the epigenetic crosstalk are not fully understood, unraveling their precise regulation is important not only for understanding the underpinnings of cellular development and cancer, but also for the design of clinically relevant and efficient therapeutics using stem cells and anticancer drugs that target tumor initiating cells.

          Related collections

          Author and article information

          Journal
          Mutat Res
          Mutation research
          Elsevier BV
          0027-5107
          0027-5107
          Dec 01 2008
          : 647
          : 1-2
          Affiliations
          [1 ] Department of Biochemistry & Molecular Biology, University of Florida, Gainesville, FL 32610, USA.
          Article
          S0027-5107(08)00179-6 NIHMS81546
          10.1016/j.mrfmmm.2008.08.006
          2647981
          18778722
          411a7230-73a7-4a7d-a724-504ca6c6ac52
          History

          Comments

          Comment on this article