1996
DOI: 10.1002/(sici)1097-0045(1996)6+<36::aid-pros8>3.0.co;2-i
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DNA methylation, molecular genetic, and linkage studies in prostate cancer

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Cited by 23 publications
(7 citation statements)
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“…In the process of homocysteine catabolism, cysteine, a main component for the synthesis of glutathione, is generated. Glutathione serves as an important cofactor of the glutathione S-transferases and glutathione peroxidases, which function in the detoxification of many toxic or carcinogenic compounds (5,36). Decreased activity of these enzymes has been associated with increased DNA (37).…”
Section: Discussionmentioning
confidence: 99%
“…In the process of homocysteine catabolism, cysteine, a main component for the synthesis of glutathione, is generated. Glutathione serves as an important cofactor of the glutathione S-transferases and glutathione peroxidases, which function in the detoxification of many toxic or carcinogenic compounds (5,36). Decreased activity of these enzymes has been associated with increased DNA (37).…”
Section: Discussionmentioning
confidence: 99%
“…Furthermore, low PLP concentrations cause a decreased enzyme activity of serine hydroxymethyltransferase, which results in a lack of methylene groups for 5,10-methylenetetrahydrofolate production (61). This may lead to increased chromosome strand breaks (62), impaired DNA repair (63,64), and DNA hypomethylation (65,66), which has been observed in different types of tumors. The majority of previous studies on genetic variations related to one-carbon metabolism in GC focused on the MTHFR gene and were mainly conducted in Asian populations (24).…”
Section: Mechanismmentioning
confidence: 99%
“…When, as a consequence of DNA methylation, tumor suppressor genes or growthinhibiting genes are down-regulated, cancer progression can be promoted (Bird, 1996;Zingg and Jones, 1997). Also for prostate cancer, CpG methylation has been described to be a mechanism that inactivates several genes (Jarrard et al, 1996;Schulz, 1998), including the E-cadherin (Graff et al, 1995) and GSTP1 genes (Lee et al, 1997). These observations were the motivation for a previous study that was to investigate whether and to what extent methylation of the CD44 promoter was correlated with loss or decrease of its expression.…”
mentioning
confidence: 99%