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Sökning: onr:"swepub:oai:gup.ub.gu.se/52529" > Low expression of r...

Low expression of reduced folate carrier-1 and folylpolyglutamate synthase correlates with lack of a deleted in colorectal carcinoma mRNA splice variant in normal-appearing mucosa of colorectal carcinoma patients

Wettergren, Yvonne, 1957 (författare)
Odin, Elisabeth, 1955 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för de kirurgiska disciplinerna, Avdelningen för kirurgi,Institute of Surgical Sciences, Department of Surgery,University of Gothenburg
Nilsson, Staffan, 1956 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för matematiska vetenskaper, matematisk statistik,Department of Mathematical Sciences, Mathematical Statistics,University of Gothenburg,Chalmers tekniska högskola,Chalmers University of Technology
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Willen, Roger, 1939 (författare)
Uppsala universitet,Institutionen för genetik och patologi
Carlsson, Göran, 1951 (författare)
Gustavsson, Bengt, 1947 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för de kirurgiska disciplinerna, Avdelningen för kirurgi,Institute of Surgical Sciences, Department of Surgery,University of Gothenburg
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 (creator_code:org_t)
Elsevier BV, 2005
2005
Engelska.
Ingår i: Cancer Detect Prev. - : Elsevier BV. - 0361-090X .- 1525-1500. ; 29:4, s. 348-55
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • BACKGROUND: Cellular folate deficiency leads to DNA strand breaks, mutations, and aberrant methylation and might be a risk factor for colorectal cancer (CRC). The putative tumor suppressor gene deleted in colorectal carcinoma (DCC) is one of several genes the expression of which seems to be affected by the folate concentration at the tissue level. Decreased expression of DCC may be caused by LOH or hypermethylation, i.e. by events that might be linked to folate deficiency. The purpose of this study was to analyze if the folate level and the gene expression levels of reduced folate carrier (RFC-1) and folylpolyglutamate synthase (FPGS) had impact on the expression of DCC splice variants. METHODS: Quantification of RFC-1 and FPGS expression in mucosa of 53 CRC patients was performed using real-time PCR whereas DCC splicing variants were detected by automated capillary gel electrophoresis. Total reduced folate concentration was measured with the FdUMP-binding assay (n = 22). RESULTS: Significantly higher expression levels of RFC-1 (p = 0.026) and FPGS (p = 0.05) were found in mucosa expressing the splice variant DCC342 compared to mucosa that did not. Furthermore, multivariate analysis showed that RFC-1 and FPGS (r = 0.49, p = 0.01) as well as folate and RFC-1 (r = 0.56, p = 0.023) were correlated only in mucosa expressing DCC342. CONCLUSIONS: In conclusion, the present study points to a potential influence of folates in regulating DCC expression at multiple levels involving post-transcriptional pathways. The results may provide a basis for a detailed investigation of molecular mechanisms involved in folate regulation of DCC expression.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Kirurgi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Surgery (hsv//eng)

Nyckelord

Adenocarcinoma/chemistry/*genetics/pathology
Adult
Aged
Aged
80 and over
*Alternative Splicing
Amino Acid Sequence
Colorectal Neoplasms/chemistry/*genetics/pathology
Female
Folic Acid Deficiency/genetics
Gene Expression Regulation
Neoplastic
Genes
DCC/genetics
Humans
Intestinal Mucosa/*chemistry
Male
Membrane Transport Proteins/analysis/*genetics
Middle Aged
Molecular Sequence Data
Multivariate Analysis
Peptide Synthases/analysis/*genetics
RNA
Neoplasm/*genetics
Reverse Transcriptase Polymerase Chain Reaction
Sweden
Neoplasm/*genetics

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