Source:http://linkedlifedata.com/resource/pubmed/id/17192059
Subject | Predicate | Object | Context |
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pubmed-article:17192059 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:17192059 | lifeskim:mentions | umls-concept:C1527249 | lld:lifeskim |
pubmed-article:17192059 | lifeskim:mentions | umls-concept:C1519302 | lld:lifeskim |
pubmed-article:17192059 | lifeskim:mentions | umls-concept:C0443343 | lld:lifeskim |
pubmed-article:17192059 | pubmed:issue | 1-2 | lld:pubmed |
pubmed-article:17192059 | pubmed:dateCreated | 2006-12-28 | lld:pubmed |
pubmed-article:17192059 | pubmed:abstractText | Chemotherapy for colorectal cancer is currently offered to patients based on the stage of their cancer, and there is evidence to show an overall survival benefit with 5-fluorouracil-based (5-FU) therapy for patients with lymph node metastasis who receive it. The pathogenesis of colorectal cancer involves genomic instability, with about 15% of tumors demonstrating a form of genomic instability called high-frequency microsatellite instability (MSI-H) and due to loss of DNA mismatch repair function, and the remainder of colorectal tumors lacking MSI-H with retained DNA mismatch repair function and called microsatellite stable (MSS), with a large proportion of these tumors demonstrating another form of genomic instability called chromosomal instability. There is now evidence to show that the form of genomic instability that is present in a patient's colorectal cancer may predict a survival benefit from 5-FU. In particular, patients whose colorectal tumors have MSI-H do not gain a survival benefit with 5-FU as compared to patients with MSS tumors. In vitro evidence supports these findings, as MSI-H colon cancer cell lines are more resistant to 5-FU compared to MSS cell lines. More specifically, components of the DNA mismatch repair system have been shown to recognize and bind to 5-FU that becomes incorporated into DNA and which could be a trigger to induce cell death. The binding and subsequent cell death events would be absent in colorectal tumors with MSI-H, which have lost intact DNA mismatch repair function. These findings suggest that: (a) tumor cytotoxicity of 5-FU is mediated by DNA mechanisms in addition to well-known RNA mechanisms, and (b) patients whose tumors demonstrate MSI-H may not benefit from 5-FU therapy. Future studies should include a better understanding of the cellular mechanisms of the DNA recognition of 5-FU, multi-centered prospective trials investigating the survival benefit of 5-FU based on genomic instability, and the investigation of alternative chemotherapeutic regimens for patients with MSI-H tumors to improve survival. | lld:pubmed |
pubmed-article:17192059 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17192059 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17192059 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17192059 | pubmed:language | eng | lld:pubmed |
pubmed-article:17192059 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17192059 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:17192059 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17192059 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:17192059 | pubmed:issn | 1574-0153 | lld:pubmed |
pubmed-article:17192059 | pubmed:author | pubmed-author:CarethersJohn... | lld:pubmed |
pubmed-article:17192059 | pubmed:author | pubmed-author:JoWon-SeokWS | lld:pubmed |
pubmed-article:17192059 | pubmed:issnType | lld:pubmed | |
pubmed-article:17192059 | pubmed:volume | 2 | lld:pubmed |
pubmed-article:17192059 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:17192059 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:17192059 | pubmed:pagination | 51-60 | lld:pubmed |
pubmed-article:17192059 | pubmed:dateRevised | 2011-9-22 | lld:pubmed |
pubmed-article:17192059 | pubmed:meshHeading | pubmed-meshheading:17192059... | lld:pubmed |
pubmed-article:17192059 | pubmed:meshHeading | pubmed-meshheading:17192059... | lld:pubmed |
pubmed-article:17192059 | pubmed:meshHeading | pubmed-meshheading:17192059... | lld:pubmed |
pubmed-article:17192059 | pubmed:meshHeading | pubmed-meshheading:17192059... | lld:pubmed |
pubmed-article:17192059 | pubmed:meshHeading | pubmed-meshheading:17192059... | lld:pubmed |
pubmed-article:17192059 | pubmed:year | 2006 | lld:pubmed |
pubmed-article:17192059 | pubmed:articleTitle | Chemotherapeutic implications in microsatellite unstable colorectal cancer. | lld:pubmed |
pubmed-article:17192059 | pubmed:affiliation | Department of Medicine, University of California, and VA San Diego Healthcare System, CA 92161, USA. | lld:pubmed |
pubmed-article:17192059 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:17192059 | pubmed:publicationType | Review | lld:pubmed |
pubmed-article:17192059 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
pubmed-article:17192059 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |