pubmed-article:21455236 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:21455236 | lifeskim:mentions | umls-concept:C1337112 | lld:lifeskim |
pubmed-article:21455236 | lifeskim:mentions | umls-concept:C0086860 | lld:lifeskim |
pubmed-article:21455236 | lifeskim:mentions | umls-concept:C1517336 | lld:lifeskim |
pubmed-article:21455236 | lifeskim:mentions | umls-concept:C0679199 | lld:lifeskim |
pubmed-article:21455236 | lifeskim:mentions | umls-concept:C0599894 | lld:lifeskim |
pubmed-article:21455236 | lifeskim:mentions | umls-concept:C0679622 | lld:lifeskim |
pubmed-article:21455236 | lifeskim:mentions | umls-concept:C0205314 | lld:lifeskim |
pubmed-article:21455236 | pubmed:issue | 4 | lld:pubmed |
pubmed-article:21455236 | pubmed:dateCreated | 2011-4-1 | lld:pubmed |
pubmed-article:21455236 | pubmed:abstractText | G-quadruplexes are four-stranded DNA structures that are over-represented in gene promoter regions and are viewed as emerging therapeutic targets in oncology, as transcriptional repression of oncogenes through stabilization of these structures could be a novel anticancer strategy. Many gene promoter G-quadruplexes have physicochemical properties and structural characteristics that might make them druggable, and their structural diversity suggests that a high degree of selectivity might be possible. Here, we describe the evidence for G-quadruplexes in gene promoters and discuss their potential as therapeutic targets, as well as progress in the development of strategies to harness this potential through intervention with small-molecule ligands. | lld:pubmed |
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