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Title:Expression of LOC285758, a potential long non-coding biomarker, is methylation- dependent and correlates with glioma malignancy grade
Authors:ID Matjašič, Alenka (Author)
ID Popović, Mara (Author)
ID Matos, Boštjan (Author)
ID Glavač, Damjan (Author)
Files:URL URL - Source URL, visit https://www.degruyter.com/downloadpdf/j/raon.ahead-of-print/raon-2017-0004/raon-2017-0004.pdf
 
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MD5: A33B71068A2597F45A725AEAFAF42D3A
 
Language:English
Typology:1.01 - Original Scientific Article
Organization:Logo OI - Institute of Oncology
Abstract:Background. Identifying the early genetic drivers can help diagnose glioma tumours in their early stages, before becoming malignant. However, there is emerging evidence that disturbance of epigenetic mechanisms also con- tributes to cell's malignant transformation and cancer progression. Long non-coding RNAs are one of key epigenetic modulators of signalling pathways, since gene expression regulation is one of their canonical mechanisms. The aim of our study was to search new gliomagenesis-specific candidate lncRNAs involved in epigenetic regulation. Patients and methods. We used a microarray approach to detect expression profiles of epigenetically involved lncRNAs on a set of 12 glioma samples, and selected LOC285758 for further qPCR expression validation on 157 glioma samples of different subtypes. To establish if change in expression is a consequence of epigenetic alterations we determined methylation status of lncRNA's promoter using MS-HRM. Additionally, we used the MLPA analysis for de- termining the status of known glioma biomarkers and used them for association analyses. Results. In all glioma subtypes levels of LOC285758 were significantly higher in comparison to normal brain reference RNA, and expression was inversely associated with promoter methylation. Expression substantially differs between astrocytoma and oligodendroglioma, and is elevated in higher WHO grades, which also showed loss of methylation. Conclusions. Our study revealed that lncRNA LOC285758 changed expression in glioma is methylation-dependent and methylation correlates with WHO malignancy grade. Methylation is also distinctive between astrocytoma I-III and other glioma subtypes and may thus serve as an additional biomarker in glioma diagnosis.
Keywords:glioma, epigenetics, methylation
Publication status:Published
Publication version:Version of Record
Publication date:01.01.2017
Publisher:Association of Radiology and Oncology
Year of publishing:2017
Number of pages:str. 331-341, IX
Numbering:Vol. 51, no. 3
Source:Ljubljana
PID:20.500.12556/DiRROS-19032 New window
UDC:616
ISSN on article:1318-2099
DOI:10.1515/raon-2017-0004 New window
COBISS.SI-ID:33350617 New window
Copyright:by Authors
Note:Soavtorji: Mara Popovic, Boštjan Matos and Damjan Glavac;
Publication date in DiRROS:03.06.2024
Views:115
Downloads:109
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Record is a part of a journal

Title:Radiology and oncology
Shortened title:Radiol. oncol.
Publisher:Slovenian Medical Society - Section of Radiology, Croatian Medical Association - Croatian Society of Radiology
ISSN:1318-2099
COBISS.SI-ID:32649472 New window

Secondary language

Language:Slovenian
Keywords:gliom, epigenetika, metilacija


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