4.6 Article

Characteristics of HPV integration in cervical adenocarcinoma and squamous carcinoma

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SPRINGER
DOI: 10.1007/s00432-023-05494-4

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HPV integration; HPV capture sequencing; Cervical adenocarcinoma; Cervical squamous carcinoma; Characterization of integration; Carcinogenesis of HPV integration

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This study aimed to investigate the characteristics of HPV integration in cervical adenocarcinoma and cervical squamous carcinoma. The results revealed that STARD3 and ERBB2 were the hotspot genes of HPV integration in adenocarcinoma, while RNA45S rDNA and MIR3648-1 were the hotspot genes in squamous carcinoma. Additionally, the study found that the expression of the most frequently integrated genes increased after integration, suggesting the significance of integration in the development of cervical cancer.
Purpose HPV integration usually occurs in HPV-related cancer, and is the main cause of cancer. But the carcinogenic mechanism of HPV integration is unclear. The study aims to provide a theoretical basis for understanding the pathogenesis of cervical adenocarcinoma (AC) and cervical squamous carcinoma (SCC). Methods We used HPV capture sequencing to obtain HPV integration sites in AC and SCC, and analyzed cytobands, distribution of genetic and genomic elements, identified integration hotspot genes, clinicopathological parameters, breakpoints of HPV16 and performed pathway analysis. Then we conducted immuno histochemical (IHC) assay to preliminarily verify the expression of most frequently integrated genes in AC, STARD3 and ERBB2. Results The results revealed that the most frequently observed integrated cytoband was 17q12 in AC and 21p11.2 in SCC, respectively. The breakpoints in both AC and SCC were more tended to occur within gene regions, compared to intergenetic regions. Compared to SCC samples, AC samples had a higher prevalence of genomic elements. In AC, HPV integration has no significantly difference with clinicopathological parameters, but in SCC integration correlated with differentiation (P < 0.05). Breakpoints of HPV in SCC located in LCR more frequently compared to AC, which destroyed the activation of promoter p97. Hotspot genes of HPV integration were STARD3 and ERBB2 in AC, and RNA45S rDNA and MIR3648-1 in SCC, respectively. Meanwhile, we preliminarily proved that the expression of STARD3 and ERBB2, the most frequently integrated genes, would increase after integration. Conclusion These results suggested that HPV may utilize the powerful hosts' promoters to express viral oncogenes and overexpression of viral oncogenes plays a significant role in the carcinogenesis of SCC. In AC, HPV integration may affect hosts' oncogenes, and the dysregulation of oncogenes may primarily contribute to progression of AC.

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