Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/21101
Title: The MLH1 polymorphism rs1800734 and risk of endometrial cancer with microsatellite instability
Authors: Lewis, A
Russell, H
Kedzierska, K
Buchanan, D
Thomas, R
Tham, E
Mints, M
Keranen, A
Giles, G
Southey, M
Milne, R
Tomlinson, I
Church, D
Spurdle, A
O'Mara, T
Keywords: endometrial cancer;mismatch repair pathway;microsatellite instability;single nucleotide polymorphism;MLH1;rs1800734
Issue Date: 8-Jul-2020
Publisher: BMC
Citation: Russell, H., Kedzierska, K., Buchanan, D.D., Thomas, R., Tham, E., Mints, M., Keränen, A., Giles, G.G., Southey, M.C., Milne, R.L., Tomlinson, I., Church, D., Spurdle, A.B. O’Mara, T.A. and Lewis, A. (2020) 'The MLH1 polymorphism rs1800734 and risk of endometrial cancer with microsatellite instability', Clinical Epigenetics 12, 102, pp. 1-9. https://doi.org/10.1186/s13148-020-00889-3
Abstract: © The Author(s) 2020. Both colorectal (CRC, 15%) and endometrial cancers (EC, 30%) exhibit microsatellite instability (MSI) due to MLH1 hypermethylation and silencing. The MLH1 promoter polymorphism, rs1800734 is associated with MSI CRC risk, increased methylation and reduced MLH1 expression. In EC samples, we investigated rs1800734 risk using MSI and MSS cases and controls. We found no evidence that rs1800734 or other MLH1 SNPs were associated with the risk of MSI EC. We found the rs1800734 risk allele had no effect on MLH1 methylation or expression in ECs. We propose that MLH1 hypermethylation occurs by different mechanisms in CRC and EC.
URI: https://bura.brunel.ac.uk/handle/2438/21101
ISSN: 1868-7075
Appears in Collections:Dept of Life Sciences Research Papers

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