Cargando…

Putative biomarkers of malignant transformation of sinonasal inverted papilloma into squamous cell carcinoma

OBJECTIVE: To compare genome-wide DNA methylation between samples of sinonasal inverted papilloma (SNIP) and squamous cell carcinoma (SCC) samples in order to identify aberrantly methylated genes that might be involved in malignant transformation. METHODS: Tissue samples were collected from patients...

Descripción completa

Detalles Bibliográficos
Autores principales: Yang, Zheng, Zhang, Yang, Wang, Xiangdong, Huang, Junwei, Guo, Wei, Wei, Peng, Li, Guojun, Wang, Ziqiao, Huang, Zhigang, Zhang, Luo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6567723/
https://www.ncbi.nlm.nih.gov/pubmed/30991875
http://dx.doi.org/10.1177/0300060519838385
_version_ 1783427141331845120
author Yang, Zheng
Zhang, Yang
Wang, Xiangdong
Huang, Junwei
Guo, Wei
Wei, Peng
Li, Guojun
Wang, Ziqiao
Huang, Zhigang
Zhang, Luo
author_facet Yang, Zheng
Zhang, Yang
Wang, Xiangdong
Huang, Junwei
Guo, Wei
Wei, Peng
Li, Guojun
Wang, Ziqiao
Huang, Zhigang
Zhang, Luo
author_sort Yang, Zheng
collection PubMed
description OBJECTIVE: To compare genome-wide DNA methylation between samples of sinonasal inverted papilloma (SNIP) and squamous cell carcinoma (SCC) samples in order to identify aberrantly methylated genes that might be involved in malignant transformation. METHODS: Tissue samples were collected from patients. DNA methylation in C-phosphate-G islands and gene promoters was analysed using a DNA methylation microarray kit. The levels of mRNA or protein from aberrantly methylated genes were measured using real-time polymerase chain reaction or Western blot analysis. RESULTS: A total of 27 tissue samples were included in this study; 15 SNIP samples and 12 SCCs arising in SNIPs. A total of 11 201 nominally differentially methylated sites were observed between SNIP and SCC arising in SNIPs. Six sites were significantly different at P < 0.01 and contained three genes (MIR661, PLEC and OPA3). These three genes were hypermethylated. In addition, the levels of mature miR-661 mRNA and PLEC protein were significantly upregulated in SCC tissues compared with SNIP samples. The levels of OPA3 protein were downregulated in SCC tissues compared with SNIP samples. CONCLUSIONS: This study demonstrated hypermethylation and abnormal expression of the MIR661, PLEC and OPA3 genes, suggesting a role for their involvement in the malignant transformation of SNIP.
format Online
Article
Text
id pubmed-6567723
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher SAGE Publications
record_format MEDLINE/PubMed
spelling pubmed-65677232019-06-20 Putative biomarkers of malignant transformation of sinonasal inverted papilloma into squamous cell carcinoma Yang, Zheng Zhang, Yang Wang, Xiangdong Huang, Junwei Guo, Wei Wei, Peng Li, Guojun Wang, Ziqiao Huang, Zhigang Zhang, Luo J Int Med Res Clinical Research Reports OBJECTIVE: To compare genome-wide DNA methylation between samples of sinonasal inverted papilloma (SNIP) and squamous cell carcinoma (SCC) samples in order to identify aberrantly methylated genes that might be involved in malignant transformation. METHODS: Tissue samples were collected from patients. DNA methylation in C-phosphate-G islands and gene promoters was analysed using a DNA methylation microarray kit. The levels of mRNA or protein from aberrantly methylated genes were measured using real-time polymerase chain reaction or Western blot analysis. RESULTS: A total of 27 tissue samples were included in this study; 15 SNIP samples and 12 SCCs arising in SNIPs. A total of 11 201 nominally differentially methylated sites were observed between SNIP and SCC arising in SNIPs. Six sites were significantly different at P < 0.01 and contained three genes (MIR661, PLEC and OPA3). These three genes were hypermethylated. In addition, the levels of mature miR-661 mRNA and PLEC protein were significantly upregulated in SCC tissues compared with SNIP samples. The levels of OPA3 protein were downregulated in SCC tissues compared with SNIP samples. CONCLUSIONS: This study demonstrated hypermethylation and abnormal expression of the MIR661, PLEC and OPA3 genes, suggesting a role for their involvement in the malignant transformation of SNIP. SAGE Publications 2019-04-16 2019-06 /pmc/articles/PMC6567723/ /pubmed/30991875 http://dx.doi.org/10.1177/0300060519838385 Text en © The Author(s) 2019 http://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Clinical Research Reports
Yang, Zheng
Zhang, Yang
Wang, Xiangdong
Huang, Junwei
Guo, Wei
Wei, Peng
Li, Guojun
Wang, Ziqiao
Huang, Zhigang
Zhang, Luo
Putative biomarkers of malignant transformation of sinonasal inverted papilloma into squamous cell carcinoma
title Putative biomarkers of malignant transformation of sinonasal inverted papilloma into squamous cell carcinoma
title_full Putative biomarkers of malignant transformation of sinonasal inverted papilloma into squamous cell carcinoma
title_fullStr Putative biomarkers of malignant transformation of sinonasal inverted papilloma into squamous cell carcinoma
title_full_unstemmed Putative biomarkers of malignant transformation of sinonasal inverted papilloma into squamous cell carcinoma
title_short Putative biomarkers of malignant transformation of sinonasal inverted papilloma into squamous cell carcinoma
title_sort putative biomarkers of malignant transformation of sinonasal inverted papilloma into squamous cell carcinoma
topic Clinical Research Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6567723/
https://www.ncbi.nlm.nih.gov/pubmed/30991875
http://dx.doi.org/10.1177/0300060519838385
work_keys_str_mv AT yangzheng putativebiomarkersofmalignanttransformationofsinonasalinvertedpapillomaintosquamouscellcarcinoma
AT zhangyang putativebiomarkersofmalignanttransformationofsinonasalinvertedpapillomaintosquamouscellcarcinoma
AT wangxiangdong putativebiomarkersofmalignanttransformationofsinonasalinvertedpapillomaintosquamouscellcarcinoma
AT huangjunwei putativebiomarkersofmalignanttransformationofsinonasalinvertedpapillomaintosquamouscellcarcinoma
AT guowei putativebiomarkersofmalignanttransformationofsinonasalinvertedpapillomaintosquamouscellcarcinoma
AT weipeng putativebiomarkersofmalignanttransformationofsinonasalinvertedpapillomaintosquamouscellcarcinoma
AT liguojun putativebiomarkersofmalignanttransformationofsinonasalinvertedpapillomaintosquamouscellcarcinoma
AT wangziqiao putativebiomarkersofmalignanttransformationofsinonasalinvertedpapillomaintosquamouscellcarcinoma
AT huangzhigang putativebiomarkersofmalignanttransformationofsinonasalinvertedpapillomaintosquamouscellcarcinoma
AT zhangluo putativebiomarkersofmalignanttransformationofsinonasalinvertedpapillomaintosquamouscellcarcinoma