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Hypermethylation of Secreted Frizzled Related Protein 1 gene promoter in different astrocytoma grades
AIM: To identify the involvement of Secreted Frizzled Related Protein 1 (SFRP1) promoter hypermethylation in different malignancy grades of astrocytoma and assess its association with beta-catenin, lymphoid-enhancer factor 1, and T-cell factor 1. METHODS: Twenty-six astrocytoma samples were collecte...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Croatian Medical Schools
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6240821/ https://www.ncbi.nlm.nih.gov/pubmed/30394013 http://dx.doi.org/10.3325/cmj.2018.59.213 |
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author | Kafka, Anja Karin-Kujundžić, Valentina Šerman, Ljiljana Bukovac, Anja Njirić, Niko Jakovčević, Antonia Pećina-Šlaus, Nives |
author_facet | Kafka, Anja Karin-Kujundžić, Valentina Šerman, Ljiljana Bukovac, Anja Njirić, Niko Jakovčević, Antonia Pećina-Šlaus, Nives |
author_sort | Kafka, Anja |
collection | PubMed |
description | AIM: To identify the involvement of Secreted Frizzled Related Protein 1 (SFRP1) promoter hypermethylation in different malignancy grades of astrocytoma and assess its association with beta-catenin, lymphoid-enhancer factor 1, and T-cell factor 1. METHODS: Twenty-six astrocytoma samples were collected from 2008-2015. Promoter hypermethylation was evaluated by methylation-specific polymerase-chain-reaction and protein expression by immunohistochemistry and stereological analysis. The staining intensity was scored by comparing immunoreactivity with normal tissue and by using 10% and 50% cut-offs. RESULTS: SFRP1 promoter methylation was found in 32% of astrocytomas. The number of hypermethylated samples increased in higher astrocytoma grades and was the highest in glioblastoma (P = 0.042 compared to other astrocytoma grades). There was 45.8% of samples with the lack of or weak expression of SFRP1 protein and 29.2% with strong expression. Samples with methylated promoter expressed significantly less SFRP1 than samples with unmethylated promoter (P = 0.031). Beta-catenin expression levels were elevated. Yet, glioblastomas with unmethylated SFRP1 promoter had significantly less beta-catenin (P = 0.033). Strong expression of lymphoid-enhancer factor 1 was associated to higher astrocytoma grades (P = 0.006). CONCLUSION: SFRP1 gene was epigenetically silenced in glioblastomas when compared to low astrocytoma grades, which may suggest that the lack of its protein is involved in astrocytoma progression. |
format | Online Article Text |
id | pubmed-6240821 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Croatian Medical Schools |
record_format | MEDLINE/PubMed |
spelling | pubmed-62408212018-11-26 Hypermethylation of Secreted Frizzled Related Protein 1 gene promoter in different astrocytoma grades Kafka, Anja Karin-Kujundžić, Valentina Šerman, Ljiljana Bukovac, Anja Njirić, Niko Jakovčević, Antonia Pećina-Šlaus, Nives Croat Med J Basic Science AIM: To identify the involvement of Secreted Frizzled Related Protein 1 (SFRP1) promoter hypermethylation in different malignancy grades of astrocytoma and assess its association with beta-catenin, lymphoid-enhancer factor 1, and T-cell factor 1. METHODS: Twenty-six astrocytoma samples were collected from 2008-2015. Promoter hypermethylation was evaluated by methylation-specific polymerase-chain-reaction and protein expression by immunohistochemistry and stereological analysis. The staining intensity was scored by comparing immunoreactivity with normal tissue and by using 10% and 50% cut-offs. RESULTS: SFRP1 promoter methylation was found in 32% of astrocytomas. The number of hypermethylated samples increased in higher astrocytoma grades and was the highest in glioblastoma (P = 0.042 compared to other astrocytoma grades). There was 45.8% of samples with the lack of or weak expression of SFRP1 protein and 29.2% with strong expression. Samples with methylated promoter expressed significantly less SFRP1 than samples with unmethylated promoter (P = 0.031). Beta-catenin expression levels were elevated. Yet, glioblastomas with unmethylated SFRP1 promoter had significantly less beta-catenin (P = 0.033). Strong expression of lymphoid-enhancer factor 1 was associated to higher astrocytoma grades (P = 0.006). CONCLUSION: SFRP1 gene was epigenetically silenced in glioblastomas when compared to low astrocytoma grades, which may suggest that the lack of its protein is involved in astrocytoma progression. Croatian Medical Schools 2018-10 /pmc/articles/PMC6240821/ /pubmed/30394013 http://dx.doi.org/10.3325/cmj.2018.59.213 Text en Copyright © 2018 by the Croatian Medical Journal. All rights reserved. http://creativecommons.org/licenses/by/2.5/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Basic Science Kafka, Anja Karin-Kujundžić, Valentina Šerman, Ljiljana Bukovac, Anja Njirić, Niko Jakovčević, Antonia Pećina-Šlaus, Nives Hypermethylation of Secreted Frizzled Related Protein 1 gene promoter in different astrocytoma grades |
title | Hypermethylation of Secreted Frizzled Related Protein 1 gene promoter in different astrocytoma grades |
title_full | Hypermethylation of Secreted Frizzled Related Protein 1 gene promoter in different astrocytoma grades |
title_fullStr | Hypermethylation of Secreted Frizzled Related Protein 1 gene promoter in different astrocytoma grades |
title_full_unstemmed | Hypermethylation of Secreted Frizzled Related Protein 1 gene promoter in different astrocytoma grades |
title_short | Hypermethylation of Secreted Frizzled Related Protein 1 gene promoter in different astrocytoma grades |
title_sort | hypermethylation of secreted frizzled related protein 1 gene promoter in different astrocytoma grades |
topic | Basic Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6240821/ https://www.ncbi.nlm.nih.gov/pubmed/30394013 http://dx.doi.org/10.3325/cmj.2018.59.213 |
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