Literature DB >> 30144395

Discovery of "folded DNA" structures in human cells: Potential drug targets.

Robert B Raffa1,2,3, Joseph V Pergolizzi3,4, Robert Taylor4, Michael H Ossipov5.   

Abstract

WHAT IS KNOWN AND
OBJECTIVE: The double-helical conformation of human DNA (hDNA) is so axiomatic that it is called the "canonical" form. Recently, though, intrastrand folds ("I-motifs" and "G-quadruplexes") have been identified in hDNA. These could be targets for novel drug discovery. COMMENT: Any interruption of the canonical form of hDNA fundamentally impacts the normal progression of transduction and translation. In particular, the synthesis of receptors and cognate protein ligands would be affected, as well as their affinity for-and signal transduction of-pharmacotherapeutic agents. Recent studies have identified normally occurring, folded structures superimposed on the usual double-helix motif of hDNA. WHAT IS NEW AND
CONCLUSION: The newly identified "folded DNA" structures ("I-motifs" and "G-quadruplexes") could represent novel drug-discovery targets, most likely for cancer.
© 2018 John Wiley & Sons Ltd.

Entities:  

Keywords:  G-quadruplex; I-motif; cancer; drug target; folded DNA

Mesh:

Substances:

Year:  2018        PMID: 30144395     DOI: 10.1111/jcpt.12758

Source DB:  PubMed          Journal:  J Clin Pharm Ther        ISSN: 0269-4727            Impact factor:   2.512


  2 in total

1.  G-quadruplex structures formed by human telomeric DNA and C9orf72 hexanucleotide repeats.

Authors:  Changdong Liu; Yanyan Geng; Haitao Miao; Xiao Shi; Yingying You; Naining Xu; Bo Zhou; Guang Zhu
Journal:  Biophys Rev       Date:  2019-05-24

2.  The crystal structure of an antiparallel chair-type G-quadruplex formed by Bromo-substituted human telomeric DNA.

Authors:  Yanyan Geng; Changdong Liu; Bo Zhou; Qixu Cai; Haitao Miao; Xiao Shi; Naining Xu; Yingying You; Chun Po Fung; Rahman Ud Din; Guang Zhu
Journal:  Nucleic Acids Res       Date:  2019-06-04       Impact factor: 16.971

  2 in total

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