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Variations in mismatch repair genes and colorectal cancer risk and clinical outcome

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00064165%3A_____%2F14%3A10282944" target="_blank" >RIV/00064165:_____/14:10282944 - isvavai.cz</a>

  • Alternative codes found

    RIV/68378041:_____/14:00430217 RIV/00064190:_____/14:#0000804 RIV/00216208:11110/14:10282944

  • Result on the web

    <a href="http://dx.doi.org/10.1093/mutage/geu014" target="_blank" >http://dx.doi.org/10.1093/mutage/geu014</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1093/mutage/geu014" target="_blank" >10.1093/mutage/geu014</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Variations in mismatch repair genes and colorectal cancer risk and clinical outcome

  • Original language description

    DNA mismatch repair (MMR) deficiency is one of the best understood forms of genetic instability in colorectal cancer (CRC). CRC is routinely cured by 5-fluorouracil (5-FU)-based chemotherapy, with a prognostic effect and resistance to such therapy conferred by MMR status. In this study, we aimed to analyse the effect of genetic variants in classical coding regions or in less-explored predicted microRNA (miRNA)-binding sites in the 3' untranslated region (3'UTR) of MMR genes on the risk of CRC, prognosisand the efficacy of 5-FU therapy. Four single nucleotide polymorphisms (SNPs) in MMR genes were initially tested for susceptibility to CRC in a case-control study (1095 cases and 1469 healthy controls). Subsequently, the same SNPs were analysed for their role in survival on a subset of patients with complete follow-up. Two SNPs in MLH3 and MSH6 were associated with clinical outcome. Among cases with colon and sigmoideum cancer, carriers of the CC genotype of rs108621 in the 3'UTR of MLH

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    EB - Genetics and molecular biology

  • OECD FORD branch

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    V - Vyzkumna aktivita podporovana z jinych verejnych zdroju

Others

  • Publication year

    2014

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Mutagenesis

  • ISSN

    0267-8357

  • e-ISSN

  • Volume of the periodical

    29

  • Issue of the periodical within the volume

    4

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    7

  • Pages from-to

    259-265

  • UT code for WoS article

    000337925200005

  • EID of the result in the Scopus database