Characterization of the genomic landscape in HPV-positive cervical and head and neck squamous cell carcinomas by whole genome next generation sequencing

dc.contributor.authorRen, Jianlan
dc.contributor.authorMa, Nian
dc.contributor.authorSeckar, Tyler
dc.contributor.authorBassa, Sheynaz
dc.contributor.authorZetola, Nicola
dc.contributor.authorGrover, Surbhi
dc.contributor.authorWei, Zhi
dc.contributor.authorRobertson, Erle
dc.date.accessioned2025-03-10T06:37:03Z
dc.date.available2025-03-10T06:37:03Z
dc.date.issued2025-03
dc.description.abstractBACKGROUND/AIM : In this study, we provide a comprehensive characterization of HPV-positive primary cervical cancers (CC) and HPV-positive head and neck squamous cell carcinomas (HNSCC) through whole genome next-generation sequencing. Human papillomavirus (HPV) infection, recognized as a definitive human carcinogen, is increasingly acknowledged for its role in development of human cancers. HPV-driven cervical cancers are among the leading causes of cancer-related deaths worldwide, while HPV-driven head and neck cancers exhibit distinct biological and clinical characteristics. Recent data has provided convincing evidence that HPV-related cervical cancer, like HPV head and neck cancer also predict better outcomes, with viral integration patterns further predicting disease related outcomes. MATERIALS AND METHODS : We designed an experimental study that encompasses four pairs of HPV-positive patient samples with controls, utilizing state-of-the-art Next Generation Sequencing (NGS) technology including whole genome sequencing, transcriptome sequencing and virus integration. RESULTS : Multiple mutated genes, including TTN, COL6A3, and FLNA, were identified shared between CC and HNSCC. Additionally, we observed a notable proportion of pathways affected by oncogenic alterations, particularly in the RTK-RAS and NOTCH pathways, in both CC and HNSCC. Furthermore, we discovered a shared down-regulation of the Hedgehog signaling pathway based on transcriptome expression analysis in KEGG. We also identified RUNX2 and TFPI as sites of virus integration, and upstream as well as downstream pathway modulators, and represent potential targets for therapeutic interventions. CONCLUSION : Overall, this study showed a thorough comparison between CC and HNSCC from multiple aspects, including gene variations, oncogenic pathways, KEGG enrichment and virus integration sites. However, further studies, which involve larger patient cohorts should be undertaken to further support these findings.en_US
dc.description.departmentMedical Oncologyen_US
dc.description.librarianhj2024en_US
dc.description.sdgSDG-03:Good heatlh and well-beingen_US
dc.description.urihttps://cgp.iiarjournals.org/en_US
dc.identifier.citationRen, J.L., Ma, N., Seckar, T. et al. 2025, 'Characterization of the genomic landscape in HPV-positive cervical and head and neck squamous cell carcinomas by whole genome next generation sequencing', Cancer Genomics & Proteomics, vol. 22, no. 2, pp. 188-207, doi : 10.21873/cgp.20496.en_US
dc.identifier.issn1109-6535 (print)
dc.identifier.issn1790-6245 (online)
dc.identifier.other10.21873/cgp.20496
dc.identifier.urihttp://hdl.handle.net/2263/101401
dc.language.isoenen_US
dc.publisherInternational Institute of Anticancer Researchen_US
dc.rights© 2025, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY-NC-ND) 4.0 international license (https://creativecommons.org/licenses/by-nc-nd/4.0).en_US
dc.subjectHPV-positive cancersen_US
dc.subjectCervical cancer (CC)en_US
dc.subjectHead and neck squamous cell carcinoma (HNSCC)en_US
dc.subjectWhole genome sequencing (WGS)en_US
dc.subjectNext-generation sequencing (NGS)en_US
dc.subjectViral integrationen_US
dc.subjectHuman papillomavirus (HPV)en_US
dc.subjectSDG-03: Good health and well-beingen_US
dc.titleCharacterization of the genomic landscape in HPV-positive cervical and head and neck squamous cell carcinomas by whole genome next generation sequencingen_US
dc.typeArticleen_US

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