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Comprehensive evaluation of one-carbon metabolism pathway gene variants and renal cell cancer risk
Authors:Gibson Todd M  Brennan Paul  Han Summer  Karami Sara  Zaridze David  Janout Vladimir  Kollarova Helen  Bencko Vladimir  Navratilova Marie  Szeszenia-Dabrowska Neonila  Mates Dana  Slamova Alena  Pfeiffer Ruth M  Stolzenberg-Solomon Rachael Z  Mayne Susan T  Yeager Meredith  Chanock Stephen  Rothman Nat  Chow Wong-Ho  Rosenberg Philip S  Boffetta Paolo  Moore Lee E
Affiliation:Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland, United States of America. gibsontm@mail.nih.gov
Abstract:

Introduction

Folate and one-carbon metabolism are linked to cancer risk through their integral role in DNA synthesis and methylation. Variation in one-carbon metabolism genes, particularly MTHFR, has been associated with risk of a number of cancers in epidemiologic studies, but little is known regarding renal cancer.

Methods

Tag single nucleotide polymorphisms (SNPs) selected to produce high genomic coverage of 13 gene regions of one-carbon metabolism (ALDH1L1, BHMT, CBS, FOLR1, MTHFR, MTR, MTRR, SHMT1, SLC19A1, TYMS) and the closely associated glutathione synthesis pathway (CTH, GGH, GSS) were genotyped for 777 renal cell carcinoma (RCC) cases and 1,035 controls in the Central and Eastern European Renal Cancer case-control study. Associations of individual SNPs (n = 163) with RCC risk were calculated using unconditional logistic regression adjusted for age, sex and study center. Minimum p-value permutation (Min-P) tests were used to identify gene regions associated with risk, and haplotypes were evaluated within these genes.

Results

The strongest associations with RCC risk were observed for SLC19A1 (Pmin-P = 0.03) and MTHFR (Pmin-P = 0.13). A haplotype consisting of four SNPs in SLC19A1 (rs12483553, rs2838950, rs2838951, and rs17004785) was associated with a 37% increased risk (p = 0.02), and exploratory stratified analysis suggested the association was only significant among those in the lowest tertile of vegetable intake.

Conclusions

To our knowledge, this is the first study to comprehensively examine variation in one-carbon metabolism genes in relation to RCC risk. We identified a novel association with SLC19A1, which is important for transport of folate into cells. Replication in other populations is required to confirm these findings.
Keywords:
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