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Distinguishing epigenetic features of preneoplastic testis tissues adjacent to seminomas and nonseminomas
PIWI pathway proteins are expressed during spermatogenesis where they play a key role in germ cell development. Epigenetic loss of PIWI proteins expression was previously demonstrated in testicular germ cell tumors (TGCTs), implying their involvement in TGCT development. In this work, apart from stu...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5008371/ https://www.ncbi.nlm.nih.gov/pubmed/26843623 http://dx.doi.org/10.18632/oncotarget.7074 |
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author | Gainetdinov, Ildar V. Kondratieva, Sofia A. Skvortsova, Yulia V. Zinovyeva, Marina V. Stukacheva, Elena A. Klimov, Alexey Tryakin, Alexey A. Azhikina, Tatyana L. |
author_facet | Gainetdinov, Ildar V. Kondratieva, Sofia A. Skvortsova, Yulia V. Zinovyeva, Marina V. Stukacheva, Elena A. Klimov, Alexey Tryakin, Alexey A. Azhikina, Tatyana L. |
author_sort | Gainetdinov, Ildar V. |
collection | PubMed |
description | PIWI pathway proteins are expressed during spermatogenesis where they play a key role in germ cell development. Epigenetic loss of PIWI proteins expression was previously demonstrated in testicular germ cell tumors (TGCTs), implying their involvement in TGCT development. In this work, apart from studying only normal testis and TGCT samples, we also analyzed an intermediate stage, i.e. preneoplastic testis tissues adjacent to TGCTs. Importantly, in this study, we minimized the contribution of patient-to-patient heterogeneity by using matched preneoplastic/TGCT samples. Surprisingly, expression of germ cell marker DDX4 suggests that spermatogenesis is retained in premalignant testis tissues adjacent to nonseminoma, but not those adjacent to seminoma. Moreover, this pattern is followed by expression of PIWI pathway genes, which impacts one of their functions: DNA methylation level over LINE-1 promoters is higher in preneoplastic testis tissues adjacent to nonseminomas than those adjacent to seminomas. This finding might imply distinct routes for development of the two types of TGCTs and could be used as a novel diagnostic marker, possibly, noninvasively. Finally, we studied the role of CpG island methylation in expression of PIWI genes in patient samples and using in vitro experiments in cell line models: a more complex interrelation between DNA methylation and expression of the corresponding genes was revealed. |
format | Online Article Text |
id | pubmed-5008371 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-50083712016-09-12 Distinguishing epigenetic features of preneoplastic testis tissues adjacent to seminomas and nonseminomas Gainetdinov, Ildar V. Kondratieva, Sofia A. Skvortsova, Yulia V. Zinovyeva, Marina V. Stukacheva, Elena A. Klimov, Alexey Tryakin, Alexey A. Azhikina, Tatyana L. Oncotarget Research Paper PIWI pathway proteins are expressed during spermatogenesis where they play a key role in germ cell development. Epigenetic loss of PIWI proteins expression was previously demonstrated in testicular germ cell tumors (TGCTs), implying their involvement in TGCT development. In this work, apart from studying only normal testis and TGCT samples, we also analyzed an intermediate stage, i.e. preneoplastic testis tissues adjacent to TGCTs. Importantly, in this study, we minimized the contribution of patient-to-patient heterogeneity by using matched preneoplastic/TGCT samples. Surprisingly, expression of germ cell marker DDX4 suggests that spermatogenesis is retained in premalignant testis tissues adjacent to nonseminoma, but not those adjacent to seminoma. Moreover, this pattern is followed by expression of PIWI pathway genes, which impacts one of their functions: DNA methylation level over LINE-1 promoters is higher in preneoplastic testis tissues adjacent to nonseminomas than those adjacent to seminomas. This finding might imply distinct routes for development of the two types of TGCTs and could be used as a novel diagnostic marker, possibly, noninvasively. Finally, we studied the role of CpG island methylation in expression of PIWI genes in patient samples and using in vitro experiments in cell line models: a more complex interrelation between DNA methylation and expression of the corresponding genes was revealed. Impact Journals LLC 2016-01-29 /pmc/articles/PMC5008371/ /pubmed/26843623 http://dx.doi.org/10.18632/oncotarget.7074 Text en Copyright: © 2016 Gainetdinov et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Gainetdinov, Ildar V. Kondratieva, Sofia A. Skvortsova, Yulia V. Zinovyeva, Marina V. Stukacheva, Elena A. Klimov, Alexey Tryakin, Alexey A. Azhikina, Tatyana L. Distinguishing epigenetic features of preneoplastic testis tissues adjacent to seminomas and nonseminomas |
title | Distinguishing epigenetic features of preneoplastic testis tissues adjacent to seminomas and nonseminomas |
title_full | Distinguishing epigenetic features of preneoplastic testis tissues adjacent to seminomas and nonseminomas |
title_fullStr | Distinguishing epigenetic features of preneoplastic testis tissues adjacent to seminomas and nonseminomas |
title_full_unstemmed | Distinguishing epigenetic features of preneoplastic testis tissues adjacent to seminomas and nonseminomas |
title_short | Distinguishing epigenetic features of preneoplastic testis tissues adjacent to seminomas and nonseminomas |
title_sort | distinguishing epigenetic features of preneoplastic testis tissues adjacent to seminomas and nonseminomas |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5008371/ https://www.ncbi.nlm.nih.gov/pubmed/26843623 http://dx.doi.org/10.18632/oncotarget.7074 |
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