Folate Levels and Polymorphisms in the Genes , and in Colorectal Cancer

Aim The aim of the study was to explore and describe the effect of polymorphisms in folate-associated genes regarding the levels of different folate forms and their distribution in tumors and mucosa in patients with colorectal cancer. Materials and Methods Tumor and mucosa tissues from 53 patients w...

Full description

Bibliographic Details
Main Authors: Helena Taflin, Yvonne Wettergren, Elisabeth Odin, Göran Carlsson, Kristoffer Derwinger
Format: Article
Language:English
Published: SAGE Publishing 2014-01-01
Series:Clinical Medicine Insights: Oncology
Online Access:https://doi.org/10.4137/CMO.S12701
id doaj-a0b8da00a48c490882620535a388e91c
record_format Article
spelling doaj-a0b8da00a48c490882620535a388e91c2020-11-25T03:43:17ZengSAGE PublishingClinical Medicine Insights: Oncology1179-55492014-01-01810.4137/CMO.S12701Folate Levels and Polymorphisms in the Genes , and in Colorectal CancerHelena Taflin0Yvonne Wettergren1Elisabeth Odin2Göran Carlsson3Kristoffer Derwinger4Sahlgrenska Academy at University of Gothenburg, Department of Surgery, Institute of Clinical Sciences, Sahlgrenska University Hospital/Östra, 41685 Gothenburg, Sweden.Sahlgrenska Academy at University of Gothenburg, Department of Surgery, Institute of Clinical Sciences, Sahlgrenska University Hospital/Östra, 41685 Gothenburg, Sweden.Sahlgrenska Academy at University of Gothenburg, Department of Surgery, Institute of Clinical Sciences, Sahlgrenska University Hospital/Östra, 41685 Gothenburg, Sweden.Sahlgrenska Academy at University of Gothenburg, Department of Surgery, Institute of Clinical Sciences, Sahlgrenska University Hospital/Östra, 41685 Gothenburg, Sweden.Sahlgrenska Academy at University of Gothenburg, Department of Surgery, Institute of Clinical Sciences, Sahlgrenska University Hospital/Östra, 41685 Gothenburg, Sweden.Aim The aim of the study was to explore and describe the effect of polymorphisms in folate-associated genes regarding the levels of different folate forms and their distribution in tumors and mucosa in patients with colorectal cancer. Materials and Methods Tumor and mucosa tissues from 53 patients with colorectal cancer were analyzed. The concentrations of tetrahydrofolate (THF), 5-methylTHF, and 5,10-methyleneTHF were measured by liquid chromatography—mass spectrometry. Genotyping of polymorphisms in the folate-associated genes methylenetetrahydrofolate reductase ( MTHFR, C677T ), methionine synthase ( MTR, A2756G ), and thymidylate synthase ( TS , 5'-TSER 28 bp tandem repeat and 3'-TSUTR 6 bp deletion/insertion), were done by real-time polymerase chain reaction. Folate levels and distributions were determined in the total patient cohort and after subgrouping by genotypes. Results The total folate level, as well as the THF and 5,10-methyleneTHF levels, were significantly higher in the tumor compared with mucosa tissue ( P = 0.030, 0.031, and 0.015, respectively). The individual variation in folate levels in both tumor and mucosa were larger than the variation found when the patients were subgrouped by the gene polymorphisms. No significant differences in the mean concentration of any folate in the mucosa or tumor tissue were found in relation to the analyzed polymorphisms. The percentage level of 5,10-methyleneTHF in tumors was highest in patients with the MTHFR 677 CC genotype, and lowest in patients with the TT genotype ( P = 0.033). A significantly lower percentage level of the 5,10-methyleneTHF level was found in tumors of patients with the 5'-TSER 3R/3R genotype ( P = 0.0031). Conclusion A significant difference was found between the percentage level of 5,10-methyleneTHF in tumor tissues in relation to the MTHFR C677T and 5'-TSER 28 bp repeat polymorphisms. However, no differences were found in the actual tissue folate levels, or in their distribution, in relation to the polymorphisms in the MTHFR, MTR , or TS genes. These findings could be of importance for further research in the field by explaining some of the difficulties of obtaining reproducible and uniform results when using a few selected polymorphisms as predictive markers.https://doi.org/10.4137/CMO.S12701
collection DOAJ
language English
format Article
sources DOAJ
author Helena Taflin
Yvonne Wettergren
Elisabeth Odin
Göran Carlsson
Kristoffer Derwinger
spellingShingle Helena Taflin
Yvonne Wettergren
Elisabeth Odin
Göran Carlsson
Kristoffer Derwinger
Folate Levels and Polymorphisms in the Genes , and in Colorectal Cancer
Clinical Medicine Insights: Oncology
author_facet Helena Taflin
Yvonne Wettergren
Elisabeth Odin
Göran Carlsson
Kristoffer Derwinger
author_sort Helena Taflin
title Folate Levels and Polymorphisms in the Genes , and in Colorectal Cancer
title_short Folate Levels and Polymorphisms in the Genes , and in Colorectal Cancer
title_full Folate Levels and Polymorphisms in the Genes , and in Colorectal Cancer
title_fullStr Folate Levels and Polymorphisms in the Genes , and in Colorectal Cancer
title_full_unstemmed Folate Levels and Polymorphisms in the Genes , and in Colorectal Cancer
title_sort folate levels and polymorphisms in the genes , and in colorectal cancer
publisher SAGE Publishing
series Clinical Medicine Insights: Oncology
issn 1179-5549
publishDate 2014-01-01
description Aim The aim of the study was to explore and describe the effect of polymorphisms in folate-associated genes regarding the levels of different folate forms and their distribution in tumors and mucosa in patients with colorectal cancer. Materials and Methods Tumor and mucosa tissues from 53 patients with colorectal cancer were analyzed. The concentrations of tetrahydrofolate (THF), 5-methylTHF, and 5,10-methyleneTHF were measured by liquid chromatography—mass spectrometry. Genotyping of polymorphisms in the folate-associated genes methylenetetrahydrofolate reductase ( MTHFR, C677T ), methionine synthase ( MTR, A2756G ), and thymidylate synthase ( TS , 5'-TSER 28 bp tandem repeat and 3'-TSUTR 6 bp deletion/insertion), were done by real-time polymerase chain reaction. Folate levels and distributions were determined in the total patient cohort and after subgrouping by genotypes. Results The total folate level, as well as the THF and 5,10-methyleneTHF levels, were significantly higher in the tumor compared with mucosa tissue ( P = 0.030, 0.031, and 0.015, respectively). The individual variation in folate levels in both tumor and mucosa were larger than the variation found when the patients were subgrouped by the gene polymorphisms. No significant differences in the mean concentration of any folate in the mucosa or tumor tissue were found in relation to the analyzed polymorphisms. The percentage level of 5,10-methyleneTHF in tumors was highest in patients with the MTHFR 677 CC genotype, and lowest in patients with the TT genotype ( P = 0.033). A significantly lower percentage level of the 5,10-methyleneTHF level was found in tumors of patients with the 5'-TSER 3R/3R genotype ( P = 0.0031). Conclusion A significant difference was found between the percentage level of 5,10-methyleneTHF in tumor tissues in relation to the MTHFR C677T and 5'-TSER 28 bp repeat polymorphisms. However, no differences were found in the actual tissue folate levels, or in their distribution, in relation to the polymorphisms in the MTHFR, MTR , or TS genes. These findings could be of importance for further research in the field by explaining some of the difficulties of obtaining reproducible and uniform results when using a few selected polymorphisms as predictive markers.
url https://doi.org/10.4137/CMO.S12701
work_keys_str_mv AT helenataflin folatelevelsandpolymorphismsinthegenesandincolorectalcancer
AT yvonnewettergren folatelevelsandpolymorphismsinthegenesandincolorectalcancer
AT elisabethodin folatelevelsandpolymorphismsinthegenesandincolorectalcancer
AT gorancarlsson folatelevelsandpolymorphismsinthegenesandincolorectalcancer
AT kristofferderwinger folatelevelsandpolymorphismsinthegenesandincolorectalcancer
_version_ 1724520951831330816