Evidence map›Paper›PMID 34526665›Full record

ArticleBritish journal of cancer2021

Multi-omics mapping of human papillomavirus integration sites illuminates novel cervical cancer target genes.

Marissa Iden, Shirng-Wern Tsaih, Yi-Wen Huang, Pengyuan Liu, Meizhu Xiao, Michael J Flister, Janet S Rader

Open access · greenAbstract read
In one paragraph

Article in British journal of cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

17 citing papers in PubMed, 22 citations in OpenAlex.

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  7. Harnessing the evolving CRISPR/Cas9 for precision oncology.Journal of translational medicine · 2024
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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

7 authors at 1 institution in 1 country.

Marissa IdenDepartment of Obstetrics and Gynecology, Medical College of Wisconsin, Milwaukee, WI, 53226, USA.ORCID http://orcid.org/0000-0003-3383-1751
Shirng-Wern TsaihDepartment of Obstetrics and Gynecology, Medical College of Wisconsin, Milwaukee, WI, 53226, USA.
Yi-Wen HuangDepartment of Obstetrics and Gynecology, Medical College of Wisconsin, Milwaukee, WI, 53226, USA.
Pengyuan LiuDepartment of Physiology, Medical College of Wisconsin, Milwaukee, WI, 53226, USA.
Meizhu XiaoDepartment of Obstetrics and Gynecology, Medical College of Wisconsin, Milwaukee, WI, 53226, USA.
Michael J FlisterGenomic Sciences and Precision Medicine Center, Medical College of Wisconsin, Milwaukee, WI, 53226, USA.
Janet S RaderDepartment of Obstetrics and Gynecology, Medical College of Wisconsin, Milwaukee, WI, 53226, USA. jrader@mcw.edu.ORCID http://orcid.org/0000-0001-7031-3385
Medical College of Wisconsin · US

Funding

Enlisting HPV integration events to illuminate drivers and target treatment in invasive cervical cancerR01CA262198 · NCI · MEDICAL COLLEGE OF WISCONSIN · PI Janet S. Rader · 2022 to 2026
$2.1M
Defining HPV integration sites of unknown significance in invasive cervical cancerR21CA241013 · NCI · MEDICAL COLLEGE OF WISCONSIN · PI RADER, JANET S. · 2020 to 2020
$401k
NCI NIH HHS R01 CA262198NCI NIH HHS R21 CA241013
6 · The paper itself

Abstract

backgroundIntegration of human papillomavirus (HPV) into the host genome is a dominant feature of invasive cervical cancer (ICC), yet the tumorigenicity of cis genomic changes at integration sites remains largely understudied.

methodsCombining multi-omics data from The Cancer Genome Atlas with patient-matched long-read sequencing of HPV integration sites, we developed a strategy for using HPV integration events to identify and prioritise novel candidate ICC target genes (integration-detected genes (IDGs)). Four IDGs were then chosen for in vitro functional studies employing small interfering RNA-mediated knockdown in cell migration, proliferation and colony formation assays.

resultsPacBio data revealed 267 unique human-HPV breakpoints comprising 87 total integration events in eight tumours. Candidate IDGs were filtered based on the following criteria: (1) proximity to integration site, (2) clonal representation of integration event, (3) tumour-specific expression (Z-score) and (4) association with ICC survival. Four candidates prioritised based on their unknown function in ICC (BNC1, RSBN1, USP36 and TAOK3) exhibited oncogenic properties in cervical cancer cell lines. Further, annotation of integration events provided clues regarding potential mechanisms underlying altered IDG expression in both integrated and non-integrated ICC tumours.

conclusionsHPV integration events can guide the identification of novel IDGs for further study in cervical carcinogenesis and as putative therapeutic targets.

Indexed as

AlphapapillomavirusCell Line, TumorCell MovementCell ProliferationDNA-Binding ProteinsFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHeLa CellsHumansPapillomavirus InfectionsProtein Serine-Threonine KinasesSurvival AnalysisTranscription FactorsUbiquitin ThiolesteraseUterine Cervical NeoplasmsBNC1 protein, humanDNA-Binding ProteinsProtein Serine-Threonine KinasesTAOK3 protein, humanTranscription FactorsUbiquitin ThiolesteraseUSP36 protein, human

Identifiers

PMID34526665
PMCPMC8575955
OpenAlexW3200643671

What OpenQuestion 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 OpenQuestion graph.