HOXA1 3′UTR Methylation Is a Potential Prognostic Biomarker in Oral Squamous cell Carcinoma
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Publication Date: | 2024 |
Other Authors: | , , , , , , |
Format: | Article |
Language: | eng |
Source: | Repositório Institucional da UNESP |
Download full: | http://dx.doi.org/10.3390/cancers16050874 https://hdl.handle.net/11449/305109 |
Summary: | Background: HOXA1 is a prognostic marker and a potential predictive biomarker for radioresistance in head and neck tumors. Its overexpression has been associated with promoter methylation and a worse prognosis in oral squamous cell carcinoma (OSCC) patients. However, opposite outcomes are also described. The effect of the methylation of this gene on different gene regions, other than the promoter, remains uncertain. We investigated the methylation profile at different genomic regions of HOXA1 in OSCC and correlated differentially methylated CpG sites with clinicopathological data. Methods: The HOXA1 DNA methylation status was evaluated by analyzing data from The Cancer Genome Atlas and three Gene Expression Omnibus datasets. Significant differentially methylated CpG sites were considered with a |∆β| ≥ 0.10 and a Bonferroni-corrected p-value < 0.01. Differentially methylated CpGs were validated by pyrosequencing using two independent cohorts of 15 and 47 OSCC patients, respectively. Results: Compared to normal tissues, we found significantly higher DNA methylation levels in the 3′UTR region of HOXA1 in OSCC. Higher methylation levels in tumor samples were positively correlated with smoking habits and patients’ overall survival. Conclusions: Our findings suggest that HOXA1 gene body methylation is a promising prognostic biomarker for OSCC with potential clinical applications in patient monitoring. |
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HOXA1 3′UTR Methylation Is a Potential Prognostic Biomarker in Oral Squamous cell CarcinomaDNA methylationhead and neck cancerHOXA1oral squamous cell carcinomatumor suppressor geneBackground: HOXA1 is a prognostic marker and a potential predictive biomarker for radioresistance in head and neck tumors. Its overexpression has been associated with promoter methylation and a worse prognosis in oral squamous cell carcinoma (OSCC) patients. However, opposite outcomes are also described. The effect of the methylation of this gene on different gene regions, other than the promoter, remains uncertain. We investigated the methylation profile at different genomic regions of HOXA1 in OSCC and correlated differentially methylated CpG sites with clinicopathological data. Methods: The HOXA1 DNA methylation status was evaluated by analyzing data from The Cancer Genome Atlas and three Gene Expression Omnibus datasets. Significant differentially methylated CpG sites were considered with a |∆β| ≥ 0.10 and a Bonferroni-corrected p-value < 0.01. Differentially methylated CpGs were validated by pyrosequencing using two independent cohorts of 15 and 47 OSCC patients, respectively. Results: Compared to normal tissues, we found significantly higher DNA methylation levels in the 3′UTR region of HOXA1 in OSCC. Higher methylation levels in tumor samples were positively correlated with smoking habits and patients’ overall survival. Conclusions: Our findings suggest that HOXA1 gene body methylation is a promising prognostic biomarker for OSCC with potential clinical applications in patient monitoring.Molecular Oncology Research Center Barretos Cancer HospitalDepartment of Biosciences and Oral Diagnosis Institute of Science and Technology São Paulo State University (UNESP)International Research Center A.C. Camargo Cancer CenterHead and Neck Surgery and Otorhinolaryngology Department AC Camargo Cancer Center Latin American Cooperative Oncology GroupHead and Neck Surgery Department and LIM 28 University of São Paulo Medical SchoolCenter for Translational Research in Oncology Cancer Institute of the State of São Paulo (ICESP)Clinical Hospital of the University of Sao Paulo Medical School (HCFMUSP)Department of Clinical Genetics University Hospital of Southern DenmarkInstitute of Regional Health Research University of Southern DenmarkDepartment of Biosciences and Oral Diagnosis Institute of Science and Technology São Paulo State University (UNESP)Barretos Cancer HospitalUniversidade Estadual Paulista (UNESP)A.C. Camargo Cancer CenterLatin American Cooperative Oncology GroupUniversidade de São Paulo (USP)Cancer Institute of the State of São Paulo (ICESP)University Hospital of Southern DenmarkUniversity of Southern DenmarkSorroche, Bruna PereiraMiranda, Keila Cristina [UNESP]Beltrami, Caroline MoraesArantes, Lidia Maria Rebolho BatistaKowalski, Luiz PauloMarchi, Fabio AlbuquerqueRogatto, Silvia ReginaAlmeida, Janete Dias [UNESP]2025-04-29T20:02:01Z2024-03-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.3390/cancers16050874Cancers, v. 16, n. 5, 2024.2072-6694https://hdl.handle.net/11449/30510910.3390/cancers160508742-s2.0-85187467972Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengCancersinfo:eu-repo/semantics/openAccess2025-04-30T14:35:16Zoai:repositorio.unesp.br:11449/305109Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462025-04-30T14:35:16Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
HOXA1 3′UTR Methylation Is a Potential Prognostic Biomarker in Oral Squamous cell Carcinoma |
title |
HOXA1 3′UTR Methylation Is a Potential Prognostic Biomarker in Oral Squamous cell Carcinoma |
spellingShingle |
HOXA1 3′UTR Methylation Is a Potential Prognostic Biomarker in Oral Squamous cell Carcinoma Sorroche, Bruna Pereira DNA methylation head and neck cancer HOXA1 oral squamous cell carcinoma tumor suppressor gene |
title_short |
HOXA1 3′UTR Methylation Is a Potential Prognostic Biomarker in Oral Squamous cell Carcinoma |
title_full |
HOXA1 3′UTR Methylation Is a Potential Prognostic Biomarker in Oral Squamous cell Carcinoma |
title_fullStr |
HOXA1 3′UTR Methylation Is a Potential Prognostic Biomarker in Oral Squamous cell Carcinoma |
title_full_unstemmed |
HOXA1 3′UTR Methylation Is a Potential Prognostic Biomarker in Oral Squamous cell Carcinoma |
title_sort |
HOXA1 3′UTR Methylation Is a Potential Prognostic Biomarker in Oral Squamous cell Carcinoma |
author |
Sorroche, Bruna Pereira |
author_facet |
Sorroche, Bruna Pereira Miranda, Keila Cristina [UNESP] Beltrami, Caroline Moraes Arantes, Lidia Maria Rebolho Batista Kowalski, Luiz Paulo Marchi, Fabio Albuquerque Rogatto, Silvia Regina Almeida, Janete Dias [UNESP] |
author_role |
author |
author2 |
Miranda, Keila Cristina [UNESP] Beltrami, Caroline Moraes Arantes, Lidia Maria Rebolho Batista Kowalski, Luiz Paulo Marchi, Fabio Albuquerque Rogatto, Silvia Regina Almeida, Janete Dias [UNESP] |
author2_role |
author author author author author author author |
dc.contributor.none.fl_str_mv |
Barretos Cancer Hospital Universidade Estadual Paulista (UNESP) A.C. Camargo Cancer Center Latin American Cooperative Oncology Group Universidade de São Paulo (USP) Cancer Institute of the State of São Paulo (ICESP) University Hospital of Southern Denmark University of Southern Denmark |
dc.contributor.author.fl_str_mv |
Sorroche, Bruna Pereira Miranda, Keila Cristina [UNESP] Beltrami, Caroline Moraes Arantes, Lidia Maria Rebolho Batista Kowalski, Luiz Paulo Marchi, Fabio Albuquerque Rogatto, Silvia Regina Almeida, Janete Dias [UNESP] |
dc.subject.por.fl_str_mv |
DNA methylation head and neck cancer HOXA1 oral squamous cell carcinoma tumor suppressor gene |
topic |
DNA methylation head and neck cancer HOXA1 oral squamous cell carcinoma tumor suppressor gene |
description |
Background: HOXA1 is a prognostic marker and a potential predictive biomarker for radioresistance in head and neck tumors. Its overexpression has been associated with promoter methylation and a worse prognosis in oral squamous cell carcinoma (OSCC) patients. However, opposite outcomes are also described. The effect of the methylation of this gene on different gene regions, other than the promoter, remains uncertain. We investigated the methylation profile at different genomic regions of HOXA1 in OSCC and correlated differentially methylated CpG sites with clinicopathological data. Methods: The HOXA1 DNA methylation status was evaluated by analyzing data from The Cancer Genome Atlas and three Gene Expression Omnibus datasets. Significant differentially methylated CpG sites were considered with a |∆β| ≥ 0.10 and a Bonferroni-corrected p-value < 0.01. Differentially methylated CpGs were validated by pyrosequencing using two independent cohorts of 15 and 47 OSCC patients, respectively. Results: Compared to normal tissues, we found significantly higher DNA methylation levels in the 3′UTR region of HOXA1 in OSCC. Higher methylation levels in tumor samples were positively correlated with smoking habits and patients’ overall survival. Conclusions: Our findings suggest that HOXA1 gene body methylation is a promising prognostic biomarker for OSCC with potential clinical applications in patient monitoring. |
publishDate |
2024 |
dc.date.none.fl_str_mv |
2024-03-01 2025-04-29T20:02:01Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.3390/cancers16050874 Cancers, v. 16, n. 5, 2024. 2072-6694 https://hdl.handle.net/11449/305109 10.3390/cancers16050874 2-s2.0-85187467972 |
url |
http://dx.doi.org/10.3390/cancers16050874 https://hdl.handle.net/11449/305109 |
identifier_str_mv |
Cancers, v. 16, n. 5, 2024. 2072-6694 10.3390/cancers16050874 2-s2.0-85187467972 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Cancers |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
repositoriounesp@unesp.br |
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1834482816358809600 |