| Literature DB >> 30412241 |
Fumihiko Takeuchi1, Iwao Kukimoto2, Zhiqiang Li3,4,5,6, Shuang Li7, Ni Li8, Zhibin Hu9,10, Atsushi Takahashi11,12, Shusaku Inoue13, Sana Yokoi14,15, Jianhua Chen4,5,16, Dong Hang9, Makoto Kuroda17, Fumihiko Matsuda18, Mika Mizuno19, Seiichiro Mori2, Peng Wu7, Naotake Tanaka20, Keitaro Matsuo13,21, Yoichiro Kamatani11,18, Michiaki Kubo22, Ding Ma7, Yongyong Shi3,4,5,6,16.
Abstract
The development of cervical cancer is initiated by human papillomavirus (HPV) infection and involves both viral and host genetic factors. Genome-wide association studies (GWAS) of cervical cancer have identified associations in the HLA locus and two loci outside HLA, but the principal genes that control infection and pathogenesis have not been identified. In the present study, we performed GWAS of cervical cancer in East Asian populations, involving 2609 cases and 4712 controls in the discovery stage and 1461 cases and 3295 controls in the follow-up stage. We identified novel-significant associations at 5q14 with the lead single nucleotide polymorphism (SNP) rs59661306 (P = 2.4 × 10-11) and at 7p11 with the lead SNP rs7457728 (P = 1.2 × 10-8). In 5q14, the chromatin region of the GWAS-significant SNPs was found to be in contact with the promoter of the ARRDC3 (arrestin domain-containing 3) gene. In our functional studies, ARRDC3 knockdown in HeLa cells caused significant reductions in both cell growth and susceptibility to HPV16 pseudovirion infection, suggesting that ARRDC3 is involved in the infectious entry of HPV into the cell. Our study advances the understanding of host genes that are responsible for cervical cancer susceptibility and guides future research on HPV infection and cancer development.Entities:
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Year: 2019 PMID: 30412241 DOI: 10.1093/hmg/ddy390
Source DB: PubMed Journal: Hum Mol Genet ISSN: 0964-6906 Impact factor: 6.150