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Chronic lymphocytic leukemia patients with heterogeneously or fully methylated LPL promotor display longer time to treatment

Authors :
Dianna Hussmann
Lise Lotte Hansen
Iben Daugaard
Thomas Kielsgaard Kristensen
Tomasz K. Wojdacz
Thomas Stauffer Larsen
Tina E Kjeldsen
Louise Kristensen
Charlotte Guldborg Nyvold
Michael Boe Møller
Source :
Daugaard, I, Hussmann, D, Kristensen, L, Kristensen, T, Kjeldsen, T E, Nyvold, C G, Larsen, T S, Møller, M B, Hansen, L L & Wojdacz, T K 2018, ' Chronic lymphocytic leukemia patients with heterogeneously or fully methylated LPL promotor display longer time to treatment ', Epigenomics, vol. 10, no. 9, pp. 1155-1166 . https://doi.org/10.2217/epi-2018-0020
Publication Year :
2018

Abstract

AIM: We investigated whether DNA methylation regulates expression of LPL and PI3K complex genes in chronic lymphocytic leukemia (CLL) and evaluated the prognostic significance of LPL promoter methylation in CLL patients. Patients & methods: Methylation of LPL promoter was assessed in 112 patients using methylation-sensitive high-resolution melting (MS-HRM).RESULTS: Patients with a fully or heterogeneously methylated LPL promoter had significantly longer median time to treatment (p < 0.001) and 75% lower (hazard ratio: 0.25; 95% CI: 0.15-0.42; p < 0.001) risk of requirement for treatment as opposed to patients with nonmethylated promoter. Multivariate modeling confirmed independent prognostic value of these findings.CONCLUSION: Chronic lymphocytic leukemia patients with a fully or heterogeneously methylated LPL gene promoter display indolent disease course and acquisition of heterogeneous methylation of LPL promoter is insufficient to induce gene expression.

Details

Language :
English
Database :
OpenAIRE
Journal :
Daugaard, I, Hussmann, D, Kristensen, L, Kristensen, T, Kjeldsen, T E, Nyvold, C G, Larsen, T S, Møller, M B, Hansen, L L & Wojdacz, T K 2018, ' Chronic lymphocytic leukemia patients with heterogeneously or fully methylated LPL promotor display longer time to treatment ', Epigenomics, vol. 10, no. 9, pp. 1155-1166 . https://doi.org/10.2217/epi-2018-0020
Accession number :
edsair.doi.dedup.....2d834e2fe3428b7edb4b6c2f81b4d4e0
Full Text :
https://doi.org/10.2217/epi-2018-0020