Journal article
The 8q24 cancer risk variant rs6983267 shows long-range interaction with MYC in colorectal cancer
Nature genetics, Vol.41(8), pp.882-884
08/2009
DOI: 10.1038/ng.403
PMCID: PMC2763485
PMID: 19561607
Abstract
An inherited variant on chromosome 8q24, rs6983267, is significantly associated with cancer pathogenesis. We present evidence that the region harboring this variant is a transcriptional enhancer, that the alleles of rs6983267 differentially bind transcription factor 7-like 2 (TCF7L2) and that the risk region physically interacts with the MYC proto-oncogene. These data provide strong support for a biological mechanism underlying this non-protein-coding risk variant.
Details
- Title: Subtitle
- The 8q24 cancer risk variant rs6983267 shows long-range interaction with MYC in colorectal cancer
- Creators
- Mark M Pomerantz - Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts, USANasim AhmadiyehLi JiaPaula HermanMichael P VerziHarshavardhan DoddapaneniChristine A BeckwithJennifer A ChanAdam HillsMatt DavisKeluo YaoSarah M KehoeHeinz-Josef LenzChristopher A HaimanChunli YanBrian E HendersonBaruch FrenkelJordi BarretinaAdam BassJosep TaberneroJosé BaselgaMeredith M ReganJ Robert ManakRamesh ShivdasaniGerhard A CoetzeeMatthew L Freedman
- Resource Type
- Journal article
- Publication Details
- Nature genetics, Vol.41(8), pp.882-884
- DOI
- 10.1038/ng.403
- PMID
- 19561607
- PMCID
- PMC2763485
- NLM abbreviation
- Nat Genet
- ISSN
- 1061-4036
- eISSN
- 1546-1718
- Publisher
- United States
- Grant note
- K08 CA134931 / NCI NIH HHS R01 CA129435 / NCI NIH HHS 5P50CA90381 / NCI NIH HHS R01 CA109147 / NCI NIH HHS Howard Hughes Medical Institute R01 CA136924 / NCI NIH HHS P50 CA090381 / NCI NIH HHS R01 CA109147-04 / NCI NIH HHS
- Language
- English
- Date published
- 08/2009
- Academic Unit
- Stead Family Department of Pediatrics; Biology; Craniofacial Anomalies Research Center
- Record Identifier
- 9983991961702771
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