Genetic variants in C-type lectin genes are associated with colorectal cancer susceptibility 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_____%2F13%3A10192847" target="_blank" >RIV/00064165:_____/13:10192847 - isvavai.cz</a>
Alternative codes found
RIV/68378041:_____/13:00396305 RIV/00216208:11110/13:10192847
Result on the web
<a href="http://dx.doi.org/10.1002/ijc.28251" target="_blank" >http://dx.doi.org/10.1002/ijc.28251</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1002/ijc.28251" target="_blank" >10.1002/ijc.28251</a>
Alternative languages
Result language
angličtina
Original language name
Genetic variants in C-type lectin genes are associated with colorectal cancer susceptibility and clinical outcome
Original language description
Inflammatory responses play a vital role at different stages of colorectal carcinogenesis. C-type lectins mediate inflammatory/immune responses and participate in immune escape of pathogens and tumors. Our study aimed to evaluate the correlation betweenpolymorphisms in three C-type lectin genes, CD209, MBL2 and REG4, and colorectal cancer (CRC) risk and clinical outcome. We genotyped 15 potentially functional single nucleotide polymorphisms (SNPs) and assessed their associations with CRC risk in a case-control study of 1353 CRC cases and 767 healthy controls from the Czech Republic. We also analyzed these SNPs in relation to overall and event-free survival in 414 patients. Two CD209 SNPs were associated with CRC risk after adjustment for multiple comparison. Minor allele carriers of the promoter SNP rs2287886 had an increased risk of CRC (OR 1.30, 95% CI 1.08-1.56), while minor allele carriers of the 3UTR SNP, rs7248637, had a decreased risk (OR 0.74, 95% CI 0.60-0.91). Multivariate s
Czech name
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Czech description
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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
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Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2013
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
International Journal of Cancer
ISSN
0020-7136
e-ISSN
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Volume of the periodical
133
Issue of the periodical within the volume
10
Country of publishing house
US - UNITED STATES
Number of pages
9
Pages from-to
2325-2333
UT code for WoS article
000324072300007
EID of the result in the Scopus database
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