• Je něco špatně v tomto záznamu ?

MTHFR and MTRR genotype and haplotype analysis and colorectal cancer susceptibility in a case-control study from the Czech Republic

B. Pardini, R. Kumar, A. Naccarati, RB. Prasad, A. Forsti, V. Polakova, L. Vodickova, J. Novotny, K. Hemminki, P. Vodicka

. 2011 ; 721 (1) : 74-80. [pub] 20110104

Jazyk angličtina Země Nizozemsko

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/bmc12027149

Grantová podpora
NS10230 MZ0 CEP - Centrální evidence projektů

Polymorphic variants in genes involved in one-carbon metabolism, in particular of dietary folate, may modulate the risk for colorectal cancer through aberrant DNA-methylation and altered nucleotide synthesis and repair. In the present study, we have assessed the association of six polymorphisms and relative haplotypes in the MTHFR gene (rs1801133 and rs1801131) and in the MTRR gene (rs1801394, rs1532268, rs162036, and rs10380) with the risk for colorectal cancer in 666 patients and 1377 controls from the Czech Republic. We found that the 677 C>T polymorphism in the MTHFR gene significantly decreased the risk for colorectal cancer in homozygous carriers of the variant allele (OR, 0.58; 95% CI, 0.39-0.87). Also, we noted a significantly different distribution of genotypes between cases and controls for the 66A>G polymorphism in the MTRR gene. In particular, homozygous carriers of the G-containing allele of this polymorphism were at an increased risk for colorectal cancer (OR, 1.39; 95% CI, 1.04-1.85). Haplotype analysis of the two MTHFR polymorphisms showed a moderate difference in the distribution of the TA haplotype between cases and controls. In comparison to the most common haplotype (CA), the TA haplotype was associated with a decreased risk for colorectal cancer (OR, 0.84; 95% CI, 0.71-0.99). No difference in the distribution between cases and controls was observed for the haplotypes based on the four polymorphisms in the MTRR gene. The present study suggests that the 677TT genotype and the TA haplotype in the MTHFR gene may also have a role in colorectal cancer risk in the Czech population, indicating the importance of genes involved in folate metabolism with respect to cancer risk. For MTRR, additional studies on larger populations are needed to clarify the possible role of variation in this gene in colorectal carcinogenesis.

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc12027149
003      
CZ-PrNML
005      
20160426152848.0
007      
ta
008      
120816s2011 ne f 000 0#eng||
009      
AR
024    7_
$a 10.1016/j.mrgentox.2010.12.008 $2 doi
035    __
$a (PubMed)21211571
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a ne
100    1_
$a Pardini, Barbara $u Institute of Experimental Medicine, Academy of Sciences of the Czech Republic, Videnska 1083, 14200 Prague 4, Czech Republic $7 _AN058834
245    10
$a MTHFR and MTRR genotype and haplotype analysis and colorectal cancer susceptibility in a case-control study from the Czech Republic / $c B. Pardini, R. Kumar, A. Naccarati, RB. Prasad, A. Forsti, V. Polakova, L. Vodickova, J. Novotny, K. Hemminki, P. Vodicka
520    9_
$a Polymorphic variants in genes involved in one-carbon metabolism, in particular of dietary folate, may modulate the risk for colorectal cancer through aberrant DNA-methylation and altered nucleotide synthesis and repair. In the present study, we have assessed the association of six polymorphisms and relative haplotypes in the MTHFR gene (rs1801133 and rs1801131) and in the MTRR gene (rs1801394, rs1532268, rs162036, and rs10380) with the risk for colorectal cancer in 666 patients and 1377 controls from the Czech Republic. We found that the 677 C>T polymorphism in the MTHFR gene significantly decreased the risk for colorectal cancer in homozygous carriers of the variant allele (OR, 0.58; 95% CI, 0.39-0.87). Also, we noted a significantly different distribution of genotypes between cases and controls for the 66A>G polymorphism in the MTRR gene. In particular, homozygous carriers of the G-containing allele of this polymorphism were at an increased risk for colorectal cancer (OR, 1.39; 95% CI, 1.04-1.85). Haplotype analysis of the two MTHFR polymorphisms showed a moderate difference in the distribution of the TA haplotype between cases and controls. In comparison to the most common haplotype (CA), the TA haplotype was associated with a decreased risk for colorectal cancer (OR, 0.84; 95% CI, 0.71-0.99). No difference in the distribution between cases and controls was observed for the haplotypes based on the four polymorphisms in the MTRR gene. The present study suggests that the 677TT genotype and the TA haplotype in the MTHFR gene may also have a role in colorectal cancer risk in the Czech population, indicating the importance of genes involved in folate metabolism with respect to cancer risk. For MTRR, additional studies on larger populations are needed to clarify the possible role of variation in this gene in colorectal carcinogenesis.
650    _2
$a dospělí $7 D000328
650    _2
$a senioři $7 D000368
650    _2
$a senioři nad 80 let $7 D000369
650    _2
$a studie případů a kontrol $7 D016022
650    _2
$a kolorektální nádory $x genetika $7 D015179
650    _2
$a ženské pohlaví $7 D005260
650    _2
$a ferredoxin-NADP-reduktasa $x genetika $7 D005287
650    _2
$a genetická predispozice k nemoci $7 D020022
650    _2
$a genotyp $7 D005838
650    _2
$a haplotypy $7 D006239
650    _2
$a lidé $7 D006801
650    _2
$a mužské pohlaví $7 D008297
650    _2
$a methylentetrahydrofolátreduktasa (NADPH2) $x genetika $7 D042965
650    _2
$a lidé středního věku $7 D008875
650    _2
$a jednonukleotidový polymorfismus $7 D020641
651    _2
$a Česká republika $7 D018153
655    _2
$a časopisecké články $7 D016428
655    _2
$a práce podpořená grantem $7 D013485
700    1_
$a Kumar, Rajiv $u German Cancer Research Center (DKFZ), Heidelberg, Germany
700    1_
$a Naccarati, Alessio $u Institute of Experimental Medicine, Academy of Sciences of the Czech Republic, Videnska 1083, 14200 Prague 4, Czech Republic
700    1_
$a Prasad, Rashmi B. $u German Cancer Research Center (DKFZ), Heidelberg, Germany
700    1_
$a Forsti, Asta $u German Cancer Research Center (DKFZ), Heidelberg, Germany
700    1_
$a Vymetálková, Veronika $7 xx0102721 $u Institute of Experimental Medicine, Academy of Sciences of the Czech Republic, Videnska 1083, 14200 Prague 4, Czech Republic
700    1_
$a Vodičková, Ludmila $7 xx0128157 $u Institute of Experimental Medicine, Academy of Sciences of the Czech Republic, Videnska 1083, 14200 Prague 4, Czech Republic; National Institute of Public Health, Prague, Czech Republic
700    1_
$a Novotný, Jan, $d 1971- $7 jo2003184375
700    1_
$a Hemminki, Kari $u German Cancer Research Center (DKFZ), Heidelberg, Germany
700    1_
$a Vodička, Pavel $7 xx0060269 $u Institute of Experimental Medicine, Academy of Sciences of the Czech Republic, Videnska 1083, 14200 Prague 4, Czech Republic
773    0_
$w MED00003430 $t Mutation research $x 0027-5107 $g Roč. 721, č. 1 (2011), s. 74-80
856    41
$u https://pubmed.ncbi.nlm.nih.gov/21211571 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y m $z 0
990    __
$a 20120816 $b ABA008
991    __
$a 20160426152614 $b ABA008
999    __
$a ok $b bmc $g 949191 $s 784495
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2011 $b 721 $c 1 $d 74-80 $e 20110104 $i 0027-5107 $m Mutation research $n Mutat Res $x MED00003430
GRA    __
$a NS10230 $p MZ0
LZP    __
$b NLK112 $a Pubmed-20120816/11/02

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...