Oncogenic high-risk human papillomavirus (HR-
HPV) infection causes a majority of cases of
cervical cancer and pre-cancerous cervical lesions. However, the mechanisms underlying the direct evolution from HPV-16/18-infected epithelium to
cervical intraepithelial neoplasia (CIN) III, which can progress to
cervical cancer, remain poorly identified. Here, we performed
RNA-seq after
laser capture microdissection, and found that APOBEC3B was highly expressed in
cervical cancer specimens compared with CIN III with HPV-16/18
infection. Furthermore, immunohistochemical analysis confirmed that high levels of APOBEC3B were correlated with
lymph node metastasis in
cervical cancer. Subsequent experiments revealed that HPV-16 E6 could upregulate APOBEC3B through direct binding to the promoter of APOBEC3B in
cervical cancer cells. Silencing of APOBEC3B by stable
short hairpin RNA-mediated knockdown reduced the proliferative capacity of Caski and HeLa cells in vitro and in vivo, but had only a small effect on the migration and invasion of two
cervical cancer cell lines. Finally, we identified the changes in gene expression following APOBEC3B silencing in Caski cells by microarray, demonstrating a biological link between APOBEC3B and CCND1 in
cervical cancer cells. Importantly, through methyl-capture sequencing and pyrosequencing, APOBEC3B was found to affect the levels of the downstream
protein Cyclin D1 (which is encoded by the CCND1 gene) through hypomethylation of the CCND1 promoter. In conclusion, our study supports HPV-16 E6-induced APOBEC3B expression associates with proliferation of
cervical cancer cells and hypomethylation of
Cyclin D1. Thus, APOBEC3B may be a potential therapeutic target in human
cervical cancer.