Please use this identifier to cite or link to this item:
https://doi.org/10.1016/j.canlet.2008.08.001
DC Field | Value | |
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dc.title | BRAF mutation is associated with the CpG island methylator phenotype in colorectal cancer from young patients | |
dc.contributor.author | Ang, P.W. | |
dc.contributor.author | Li, W.Q. | |
dc.contributor.author | Soong, R. | |
dc.contributor.author | Iacopetta, B. | |
dc.date.accessioned | 2014-12-12T07:09:58Z | |
dc.date.available | 2014-12-12T07:09:58Z | |
dc.date.issued | 2009-01-18 | |
dc.identifier.citation | Ang, P.W., Li, W.Q., Soong, R., Iacopetta, B. (2009-01-18). BRAF mutation is associated with the CpG island methylator phenotype in colorectal cancer from young patients. Cancer Letters 273 (2) : 221-224. ScholarBank@NUS Repository. https://doi.org/10.1016/j.canlet.2008.08.001 | |
dc.identifier.issn | 03043835 | |
dc.identifier.uri | http://scholarbank.nus.edu.sg/handle/10635/115013 | |
dc.description.abstract | This study investigated the relationship between BRAF mutation, the CpG island methylator phenotype (CIMP+) and APC methylation in colorectal cancer (CRC) from young patients. The V600E BRAF mutation was found in 7% of cases and was strongly associated with the tumour features of proximal site, advanced stage and poor histological grade. More than half (53%) the tumours with BRAF mutation were also CIMP+ as evaluated by a standard panel of markers, compared to only 4% of tumours with wildtype BRAF (P < 0.0001). In contrast to CIMP+, APC methylation was inversely correlated with BRAF mutation (P = 0.02). BRAF mutation and CIMP+ are therefore likely to be involved in an alternate, albeit rare, pathway to APC inactivation during the development of CRC in younger patients. © 2008 Elsevier Ireland Ltd. All rights reserved. | |
dc.description.uri | http://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/j.canlet.2008.08.001 | |
dc.source | Scopus | |
dc.subject | APC | |
dc.subject | BRAF | |
dc.subject | CIMP | |
dc.subject | Colorectal cancer | |
dc.type | Article | |
dc.contributor.department | CANCER SCIENCE INSTITUTE OF SINGAPORE | |
dc.description.doi | 10.1016/j.canlet.2008.08.001 | |
dc.description.sourcetitle | Cancer Letters | |
dc.description.volume | 273 | |
dc.description.issue | 2 | |
dc.description.page | 221-224 | |
dc.description.coden | CALED | |
dc.identifier.isiut | 000262582100005 | |
Appears in Collections: | Staff Publications |
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