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   <subfield code="a">Genetic variants in the folate pathway and risk of childhood acute lymphoblastic leukemia</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Catherine Metayer, Ghislaine Scélo, Anand Chokkalingam, Lisa Barcellos, Melinda Aldrich, Jeffrey Chang, Neela Guha, Kevin Urayama, Helen Hansen, Gladys Block, Vincent Kiley, John Wiencke, Joseph Wiemels, Patricia Buffler]</subfield>
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   <subfield code="a">Objective: Folate is involved in the one-carbon metabolism that plays an essential role in the synthesis, repair, and methylation of DNA. We examined whether child's germline genetic variation in the folate pathway is associated with childhood acute lymphoblastic leukemia (ALL), and whether periconception maternal folate and alcohol intake modify the risk. Methods: Seventy-six single nucleotide polymorphisms (SNPs), including 66 haplotype-tagging SNPs in 10 genes (CBS, DHFR, FOLH1, MTHFD1, MTHFR, MTR, MTRR, SHMT1, SLC19A1, and TYMS), were genotyped in 377 ALL cases and 448 controls. Log-additive associations between genotypes and ALL risk were adjusted for age, sex, Hispanic ethnicity (when appropriate), and maternal race. Results: Single and haplotype SNPs analyses showed statistically significant associations between SNPs located in (or adjacent to) CBS, MTRR, TYMS/ENOFS, and childhood ALL. Many regions of CBS were associated with childhood ALL in Hispanics and non-Hispanics (p&lt;0.01). Levels of maternal folate intake modified associations with SNPs in CBS, MTRR, and TYMS. Conclusion: Our data suggest the importance of genetic variability in the folate pathway and childhood ALL risk.</subfield>
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   <subfield code="a">Springer Science+Business Media B.V., 2011</subfield>
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   <subfield code="a">Case-control study</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Children</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">DNA methylation</subfield>
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   <subfield code="a">Folate</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Genetic polymorphisms</subfield>
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   <subfield code="a">Leukemia</subfield>
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   <subfield code="u">School of Public Health, University of California, Berkeley, 1995 University Avenue, Suite 460, 94704-7392, Berkeley, CA, USA</subfield>
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   <subfield code="a">Scélo</subfield>
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   <subfield code="u">International Agency for Research on Cancer, Lyon, France</subfield>
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   <subfield code="a">Chokkalingam</subfield>
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   <subfield code="u">School of Public Health, University of California, Berkeley, Berkeley, CA, USA</subfield>
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   <subfield code="u">School of Public Health, University of California, Berkeley, Berkeley, CA, USA</subfield>
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   <subfield code="u">Division of Epidemiology, Institute for Medicine and Public Health, Vanderbilt University, Vanderbilt, TN, USA</subfield>
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   <subfield code="u">National Institute of Cancer Research, National Health Research Institutes, Tainan, Taiwan</subfield>
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   <subfield code="u">International Agency for Research on Cancer, Lyon, France</subfield>
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   <subfield code="t">Cancer Causes &amp; Control</subfield>
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   <subfield code="g">22/9(2011-09-01), 1243-1258</subfield>
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