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Genome-wide DNA methylation profiling of HPV-negative leukoplakia and gingivobuccal complex cancers
BACKGROUND: Gingivobuccal complex oral squamous cell carcinoma (GBC-OSCC) is an aggressive malignancy with high mortality often preceded by premalignant lesions, including leukoplakia. Previous studies have reported genomic drivers in OSCC, but much remains to be elucidated about DNA methylation pat...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10225107/ https://www.ncbi.nlm.nih.gov/pubmed/37245006 http://dx.doi.org/10.1186/s13148-023-01510-z |
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author | Inchanalkar, Mayuri Srivatsa, Sumana Ambatipudi, Srikant Bhosale, Priyanka G. Patil, Asawari Schäffer, Alejandro A. Beerenwinkel, Niko Mahimkar, Manoj B. |
author_facet | Inchanalkar, Mayuri Srivatsa, Sumana Ambatipudi, Srikant Bhosale, Priyanka G. Patil, Asawari Schäffer, Alejandro A. Beerenwinkel, Niko Mahimkar, Manoj B. |
author_sort | Inchanalkar, Mayuri |
collection | PubMed |
description | BACKGROUND: Gingivobuccal complex oral squamous cell carcinoma (GBC-OSCC) is an aggressive malignancy with high mortality often preceded by premalignant lesions, including leukoplakia. Previous studies have reported genomic drivers in OSCC, but much remains to be elucidated about DNA methylation patterns across different stages of oral carcinogenesis. RESULTS: There is a serious lack of biomarkers and clinical application of biomarkers for early detection and prognosis of gingivobuccal complex cancers. Hence, in search of novel biomarkers, we measured genome-wide DNA methylation in 22 normal oral tissues, 22 leukoplakia, and 74 GBC-OSCC tissue samples. Both leukoplakia and GBC-OSCC had distinct methylation profiles as compared to normal oral tissue samples. Aberrant DNA methylation increases during the different stages of oral carcinogenesis, from premalignant lesions to carcinoma. We identified 846 and 5111 differentially methylated promoters in leukoplakia and GBC-OSCC, respectively, with a sizable fraction shared between the two sets. Further, we identified potential biomarkers from integrative analysis in gingivobuccal complex cancers and validated them in an independent cohort. Integration of genome, epigenome, and transcriptome data revealed candidate genes with gene expression synergistically regulated by copy number and DNA methylation changes. Regularised Cox regression identified 32 genes associated with patient survival. In an independent set of samples, we validated eight genes (FAT1, GLDC, HOXB13, CST7, CYB5A, MLLT11, GHR, LY75) from the integrative analysis and 30 genes from previously published reports. Bisulfite pyrosequencing validated GLDC (P = 0.036), HOXB13 (P < 0.0001) promoter hypermethylation, and FAT1 (P < 0.0001) hypomethylation in GBC-OSCC compared to normal controls. CONCLUSIONS: Our findings identified methylation signatures associated with leukoplakia and gingivobuccal complex cancers. The integrative analysis in GBC-OSCC identified putative biomarkers that enhance existing knowledge of oral carcinogenesis and may potentially help in risk stratification and prognosis of GBC-OSCC. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13148-023-01510-z. |
format | Online Article Text |
id | pubmed-10225107 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-102251072023-05-29 Genome-wide DNA methylation profiling of HPV-negative leukoplakia and gingivobuccal complex cancers Inchanalkar, Mayuri Srivatsa, Sumana Ambatipudi, Srikant Bhosale, Priyanka G. Patil, Asawari Schäffer, Alejandro A. Beerenwinkel, Niko Mahimkar, Manoj B. Clin Epigenetics Research BACKGROUND: Gingivobuccal complex oral squamous cell carcinoma (GBC-OSCC) is an aggressive malignancy with high mortality often preceded by premalignant lesions, including leukoplakia. Previous studies have reported genomic drivers in OSCC, but much remains to be elucidated about DNA methylation patterns across different stages of oral carcinogenesis. RESULTS: There is a serious lack of biomarkers and clinical application of biomarkers for early detection and prognosis of gingivobuccal complex cancers. Hence, in search of novel biomarkers, we measured genome-wide DNA methylation in 22 normal oral tissues, 22 leukoplakia, and 74 GBC-OSCC tissue samples. Both leukoplakia and GBC-OSCC had distinct methylation profiles as compared to normal oral tissue samples. Aberrant DNA methylation increases during the different stages of oral carcinogenesis, from premalignant lesions to carcinoma. We identified 846 and 5111 differentially methylated promoters in leukoplakia and GBC-OSCC, respectively, with a sizable fraction shared between the two sets. Further, we identified potential biomarkers from integrative analysis in gingivobuccal complex cancers and validated them in an independent cohort. Integration of genome, epigenome, and transcriptome data revealed candidate genes with gene expression synergistically regulated by copy number and DNA methylation changes. Regularised Cox regression identified 32 genes associated with patient survival. In an independent set of samples, we validated eight genes (FAT1, GLDC, HOXB13, CST7, CYB5A, MLLT11, GHR, LY75) from the integrative analysis and 30 genes from previously published reports. Bisulfite pyrosequencing validated GLDC (P = 0.036), HOXB13 (P < 0.0001) promoter hypermethylation, and FAT1 (P < 0.0001) hypomethylation in GBC-OSCC compared to normal controls. CONCLUSIONS: Our findings identified methylation signatures associated with leukoplakia and gingivobuccal complex cancers. The integrative analysis in GBC-OSCC identified putative biomarkers that enhance existing knowledge of oral carcinogenesis and may potentially help in risk stratification and prognosis of GBC-OSCC. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13148-023-01510-z. BioMed Central 2023-05-27 /pmc/articles/PMC10225107/ /pubmed/37245006 http://dx.doi.org/10.1186/s13148-023-01510-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Inchanalkar, Mayuri Srivatsa, Sumana Ambatipudi, Srikant Bhosale, Priyanka G. Patil, Asawari Schäffer, Alejandro A. Beerenwinkel, Niko Mahimkar, Manoj B. Genome-wide DNA methylation profiling of HPV-negative leukoplakia and gingivobuccal complex cancers |
title | Genome-wide DNA methylation profiling of HPV-negative leukoplakia and gingivobuccal complex cancers |
title_full | Genome-wide DNA methylation profiling of HPV-negative leukoplakia and gingivobuccal complex cancers |
title_fullStr | Genome-wide DNA methylation profiling of HPV-negative leukoplakia and gingivobuccal complex cancers |
title_full_unstemmed | Genome-wide DNA methylation profiling of HPV-negative leukoplakia and gingivobuccal complex cancers |
title_short | Genome-wide DNA methylation profiling of HPV-negative leukoplakia and gingivobuccal complex cancers |
title_sort | genome-wide dna methylation profiling of hpv-negative leukoplakia and gingivobuccal complex cancers |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10225107/ https://www.ncbi.nlm.nih.gov/pubmed/37245006 http://dx.doi.org/10.1186/s13148-023-01510-z |
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