Characterization of the Genomic Landscape in HPV-positive Cervical and Head and Neck Squamous Cell Carcinomas by Whole Genome Next Generation Sequencing

被引:0
|
作者
Ren, Jianlan [1 ]
Ma, Nian [2 ]
Seckar, Tyler [3 ]
Bassa, Sheynaz [4 ]
Zetola, Nicola [5 ]
Grover, Surbhi [6 ]
Wei, Zhi [1 ]
Robertson, Erle [2 ]
机构
[1] New Jersey Inst Technol, Dept Comp Sci, Newark, NJ USA
[2] Univ Penn, Perelman Sch Med, Dept Otorhinolaryngol Head & Neck Surg, Philadelphia, PA 19104 USA
[3] George Washington Univ, George Washington Sch Med, Dept Canc Biol, Washington, DC USA
[4] Univ Pretoria, Steve Biko Acad Hosp, Fac Hlth Sci, Dept Radiat Oncol, Pretoria, South Africa
[5] Augusta Coll Med, Dept Med, Div Pulm Med, Augusta, GA USA
[6] Univ Penn, Perelman Sch Med, Dept Radiat Oncol, Philadelphia, PA USA
关键词
HPV-positive cancers; cervical cancer (CC); head and neck squamous cell carcinoma (HNSCC); whole genome sequencing; next-generation sequencing (NGS); viral integration; HUMAN-PAPILLOMAVIRUS; CANCER; PATHWAY; ASSOCIATION; INHIBITOR; NOTCH;
D O I
10.21873/cgp.20496
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background/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.
引用
收藏
页码:188 / 207
页数:20
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