Evidence map›Paper›PMID 29593040›Full record

ArticleJournal of virology2018

Within-Host Variations of Human Papillomavirus Reveal APOBEC Signature Mutagenesis in the Viral Genome.

Yusuke Hirose, Mamiko Onuki, Yuri Tenjimbayashi, Seiichiro Mori, Yoshiyuki Ishii, Takamasa Takeuchi, Nobutaka Tasaka, Toyomi Satoh, Tohru Morisada, Takashi Iwata and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
5.7field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

33 citing papers in PubMed, 59 citations in OpenAlex.

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  20. HPV Meets APOBEC: New Players in Head and Neck Cancer.International journal of molecular sciences · 2021
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 4 institutions in 1 country.

Yusuke HiroseDepartment of Obstetrics and Gynecology, Showa University School of Medicine, Tokyo, Japan.
Mamiko OnukiDepartment of Obstetrics and Gynecology, Showa University School of Medicine, Tokyo, Japan.
Yuri TenjimbayashiDepartment of Obstetrics and Gynecology, Showa University School of Medicine, Tokyo, Japan.
Seiichiro MoriPathogen Genomics Center, National Institute of Infectious Diseases, Tokyo, Japan.
Yoshiyuki IshiiPathogen Genomics Center, National Institute of Infectious Diseases, Tokyo, Japan.
Takamasa TakeuchiPathogen Genomics Center, National Institute of Infectious Diseases, Tokyo, Japan.
Nobutaka TasakaDepartment of Obstetrics and Gynecology, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
Toyomi SatohDepartment of Obstetrics and Gynecology, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
Tohru MorisadaDepartment of Obstetrics and Gynecology, Keio University School of Medicine, Tokyo, Japan.
Takashi IwataDepartment of Obstetrics and Gynecology, Keio University School of Medicine, Tokyo, Japan.
Shingo MiyamotoDepartment of Obstetrics and Gynecology, Showa University School of Medicine, Tokyo, Japan.
Koji MatsumotoDepartment of Obstetrics and Gynecology, Showa University School of Medicine, Tokyo, Japan.
Akihiko SekizawaDepartment of Obstetrics and Gynecology, Showa University School of Medicine, Tokyo, Japan.
Iwao KukimotoPathogen Genomics Center, National Institute of Infectious Diseases, Tokyo, Japan ikuki@nih.go.jp.
National Institute of Infectious Diseases · JPShowa University · JPKeio University · JPUniversity of Tsukuba · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Persistent infection with oncogenic human papillomaviruses (HPVs) causes cervical cancer, accompanied by the accumulation of somatic mutations into the host genome. There are concomitant genetic changes in the HPV genome during viral infection; however, their relevance to cervical carcinogenesis is poorly understood. Here, we explored within-host genetic diversity of HPV by performing deep-sequencing analyses of viral whole-genome sequences in clinical specimens. The whole genomes of HPV types 16, 52, and 58 were amplified by type-specific PCR from total cellular DNA of cervical exfoliated cells collected from patients with cervical intraepithelial neoplasia (CIN) and invasive cervical cancer (ICC) and were deep sequenced. After constructing a reference viral genome sequence for each specimen, nucleotide positions showing changes with >0.5% frequencies compared to the reference sequence were determined for individual samples. In total, 1,052 positions of nucleotide variations were detected in HPV genomes from 151 samples (CIN1,

Indexed as

APOBEC-1 DeaminaseBase SequenceCervix UteriDNA, ViralFemaleGenetic VariationGenome, ViralHigh-Throughput Nucleotide SequencingHuman papillomavirus 16HumansMutagenesisMutationPapillomavirus InfectionsSequence Analysis, DNAUterine Cervical DysplasiaUterine Cervical NeoplasmsAPOBEC-1 DeaminaseDNA, ViralAPOBECgenetic diversityhuman papillomavirusnext-generation sequencingquasispecies

Identifiers

PMID29593040
PMCPMC5974501
OpenAlexW2795241586

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.