APOBEC3A associates with human papillomavirus genome integration in oropharyngeal cancers

被引:43
作者
Kondo, S. [1 ]
Wakae, K. [2 ]
Wakisaka, N. [1 ]
Nakanishi, Y. [1 ]
Ishikawa, K. [1 ]
Komori, T. [1 ]
Moriyama-Kita, M. [1 ]
Endo, K. [1 ]
Murono, S. [1 ]
Wang, Z. [2 ,3 ]
Kitamura, K. [2 ]
Nishiyama, T. [4 ]
Yamaguchi, K. [5 ]
Shigenobu, S. [5 ]
Muramatsu, M. [2 ]
Yoshizaki, T. [1 ]
机构
[1] Kanazawa Univ, Grad Sch Med Sci, Div Otolaryngol Head & Neck Surg, 13-1 Takara Machi, Kanazawa, Ishikawa 9208640, Japan
[2] Kanazawa Univ, Grad Sch Med Sci, Dept Mol Genet, Kanazawa, Ishikawa, Japan
[3] Dalian Univ, Affiliated Zhongshan Hosp, Div Med Oncol, Dalian, Peoples R China
[4] Kanazawa Univ, Adv Sci Res Ctr, Kanazawa, Ishikawa, Japan
[5] Natl Inst Basic Biol, Funct Genom Facil, Okazaki, Aichi, Japan
关键词
SIMPLEX-VIRUS; 1; MUTATIONAL PROCESSES; CYTIDINE DEAMINASES; DNA; HYPERMUTATION; EXPRESSION; PATTERNS; TYPE-16; HEAD; RESTRICTION;
D O I
10.1038/onc.2016.335
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The prevalence of human papillomavirus (HPV)-related oropharyngeal cancers has been increasing in developed countries. We recently demonstrated that members of the apolipoprotein B mRNA-editing catalytic polypeptide 3 (APOBEC3, A3) family, which are antiviral factors, can induce hypermutation of HPV DNA in vitro. In the present study, we found numerous C-to-T and G-to-A hypermutations in the HPV16 genome in oropharyngeal cancer (OPC) biopsy samples using differential DNA denaturation PCR and next-generation sequencing. A3s were more abundantly expressed in HPV16-positive OPCs than in HPV-negative, as assessed using immunohistochemistry and reverse transcription quantitative PCR. In addition, interferons upregulated A3s in an HPV16-positive OPC cell line. Furthermore, quantitative PCR analysis of HPV DNA suggests that APOBEC3A (A3A) expression is strongly correlated with the integration of HPV DNA. These results suggest that HPV16 infection may upregulate A3A expression, thereby increasing the chance of viral DNA integration. The role of A3A in HPV-induced carcinogenesis is discussed.
引用
收藏
页码:1687 / 1697
页数:11
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