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Expression of Hedgehog ligand and signal transduction components in mutually distinct isocitrate dehydrogenase mutant glioma cells supports a role for paracrine signaling
Authors:Sunday A. Abiria  Thomas V. Williams  Alexander L. Munden  Vandana K. Grover  Ato Wallace  Christopher J. Lundberg  J. Gerardo Valadez  Michael K. Cooper
Affiliation:1. Yorkshire Regional Cytogenetics Unit, St James’s University Hospital, Leeds, LS9 7TF, UK
2. Section of Oncology and Clinical Research, Leeds Institute of Molecular Medicine, St James’s University Hospital, Leeds, LS9 7TF, UK
3. Department of Oncology, St James’s University Hospital, Leeds, LS9 7TF, UK
4. Department of Neurosurgery, Leeds General Infirmary, Leeds, LS1 3BR, UK
5. Department of Histopathology, St James’s University Hospital, Leeds, LS9 7TF, UK
6. Department of Neurosurgery, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, 02115, USA
Abstract:DNA methylation plays an important role in cancer biology and methylation events are important prognostic and predictive markers in many tumor types. We have used methylation-specific multiplex ligation-dependent probe amplification to survey the methylation status of MGMT and 25 tumor suppressor genes in 73 glioblastoma cases. The data obtained was correlated with overall survival and response to treatment. The study revealed that methylation of promoter regions in TP73 (seven patients), THBS1 (eight patients) and PYCARD (nine patients) was associated with improved outcome, whereas GATA5 (21 patients) and WT1 (24 patients) promoter methylation were associated with poor outcome. In patients treated with temozolomide and radiation MGMT and PYCARD promoter methylation events remained associated with improved survival whereas GATA5 was associated with a poor outcome. The identification of GATA5 promoter methylation in glioblastoma has not previously been reported. Furthermore, a cumulative methylation score separated patients into survival groups better than any single methylation event. In conclusion, we have identified specific methylation events associated with patient outcome and treatment response in glioblastoma, and these may be of functional and predictive/prognostic significance. This study therefore provides novel candidates and approaches for future prospective validation.
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