Evidence map›Paper›PMID 33191407›Full record

ArticleBritish journal of cancer2021

Human papilloma virus (HPV) integration signature in Cervical Cancer: identification of MACROD2 gene as HPV hot spot integration site.

Maud Kamal, Sonia Lameiras, Marc Deloger, Adeline Morel, Sophie Vacher, Charlotte Lecerf, Célia Dupain, Emmanuelle Jeannot, Elodie Girard, Sylvain Baulande and 14 more

Erratum issued Registry-linked trialOpen access · hybridAbstract 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. An erratum has been issued. It is linked to trial NCT02428842 (Biomarker Evaluation in Advanced Stage Cervical Cancer by an International Working Group. Tumor Stages), which is not on this map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
6.7field-weighted citation impact, top 2% 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.

NCT02428842 nacompletednot on this map

Biomarker Evaluation in Advanced Stage Cervical Cancer by an International Working Group. Tumor Stages (1B1 - 4)

TypeinterventionalSponsorInstitut CurieRan2013 to 2020Enrolled419ConditionsCervical CancerArmsTumor biopsies, Blood sampling
3 · Its place in the literature

Who cites it

60 citing papers in PubMed, 85 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. HPV Integration in Head and Neck Cancer: Downstream Splicing Events and Expression Ratios Linked with Poor Outcomes.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Disruption Events in the HPV18International journal of molecular sciences · 2025
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors at 20 institutions in 9 countries.

Maud KamalDepartment of Drug Development and Innovation, Institut Curie, PSL Research University, 75005 Paris & 92210, Saint-Cloud, France. maud.kamal@curie.fr.
Sonia LameirasInstitut Curie, Genomics of Excellence (ICGex) Platform, PSL Research University, 75005, Paris, France.
Marc DelogerBioinformatics and Computational Systems Biology of Cancer, PSL Research University, Mines Paris Tech, INSERM U900, 75005, Paris, France.
Adeline MorelDepartment of Genetics, Institut Curie, PSL Research University, 75005, Paris, France.
Sophie VacherDepartment of Genetics, Institut Curie, PSL Research University, 75005, Paris, France.
Charlotte LecerfDepartment of Drug Development and Innovation, Institut Curie, PSL Research University, 75005 Paris & 92210, Saint-Cloud, France.
Célia DupainDepartment of Drug Development and Innovation, Institut Curie, PSL Research University, 75005 Paris & 92210, Saint-Cloud, France.
Emmanuelle JeannotDepartment of Genetics, Institut Curie, PSL Research University, 75005, Paris, France.ORCID http://orcid.org/0000-0002-4851-7450
Elodie GirardBioinformatics and Computational Systems Biology of Cancer, PSL Research University, Mines Paris Tech, INSERM U900, 75005, Paris, France.
Sylvain BaulandeInstitut Curie, Genomics of Excellence (ICGex) Platform, PSL Research University, 75005, Paris, France.
Coraline DubotDepartment of Drug Development and Innovation, Institut Curie, PSL Research University, 75005 Paris & 92210, Saint-Cloud, France.
Gemma KenterCenter for Gynaecologic Oncology Amsterdam, Amsterdam UMC and The Netherlands Cancer Institute - Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.
Ekaterina S JordanovaCenter for Gynaecologic Oncology Amsterdam, Amsterdam UMC and The Netherlands Cancer Institute - Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.ORCID http://orcid.org/0000-0002-8121-1322
Els M J J BernsDepartment of Medical Oncology, Erasmus MC, 3000 CA, Rotterdam, The Netherlands.
Guillaume BataillonDepartment of Pathology, Institut Curie, PSL Research University, 75005, Paris, France.
Marina PopovicOncology Institute of Vojvodina, Put doktora Goldmana, 421204, Sremska Kamenica, Serbia.
Roman RouzierDepartment of Surgery, Institut Curie, PSL Research University, 92210, Saint-Cloud, France.
Wulfran CacheuxHopital Privé Pays de Savoie, Service d'oncologie médicale, 19 avenue Pierre Mendès France, 74100, Annemasse, France.
Christophe Le TourneauDepartment of Drug Development and Innovation, Institut Curie, PSL Research University, 75005 Paris & 92210, Saint-Cloud, France.ORCID http://orcid.org/0000-0001-9772-4686
Alain NicolasInstitut Curie, PSL Research University, CNRS UMR3244, 75248, Paris, France.
Nicolas ServantBioinformatics and Computational Systems Biology of Cancer, PSL Research University, Mines Paris Tech, INSERM U900, 75005, Paris, France.
Suzy M Scholl *Department of Drug Development and Innovation, Institut Curie, PSL Research University, 75005 Paris & 92210, Saint-Cloud, France.
Ivan Bièche *Department of Genetics, Institut Curie, PSL Research University, 75005, Paris, France.
RAIDs Consortium
Université Paris Sciences et Lettres · FRInstitut Curie · FRThe Netherlands Cancer Institute · NLErasmus University Rotterdam · NLInstitut Gustave Roussy · FRSeqOmics Biotechnology (Hungary) · HUInserm · FROncology Institute of Vojvodina · RSVictor Babeș University of Medicine and Pharmacy Timișoara · ROHannover Clinical Trial Center (Germany) · DEArcagy Gineco · FRCentre National de la Recherche Scientifique · FRErasmus MC · NLEuropean Clinical Research Infrastructure Network · FRInstitut Bergonié · FRRakon (France) · FRSorbonne Université · FRUniversität Greifswald · DEUniversité Joseph Fourier · FRCentre Georges François Leclerc · FR

Funding

Agence Nationale de la Recherche (French National Research Agency) France Génomique ANR-10-INBS-09-08Agence Nationale de la Recherche (French National Research Agency) ICGEx ANR-10-EQPX-03EC | EC Seventh Framework Programm | FP7 People: Marie-Curie Actions (FP7-PEOPLE - Specific Programme "People" Implementing the Seventh Framework Programme of the European Community for Research, Technological Development and Demonstration Activities (2007 to 2013)) No 304810
6 · The paper itself

Abstract

backgroundCervical cancer (CC) remains a leading cause of gynaecological cancer-related mortality with infection by human papilloma virus (HPV) being the most important risk factor. We analysed the association between different viral integration signatures, clinical parameters and outcome in pre-treated CCs.

methodsDifferent integration signatures were identified using HPV double capture followed by next-generation sequencing (NGS) in 272 CC patients from the BioRAIDs study [NCT02428842]. Correlations between HPV integration signatures and clinical, biological and molecular features were assessed.

resultsEpisomal HPV was much less frequent in CC as compared to anal carcinoma (p < 0.0001). We identified >300 different HPV-chromosomal junctions (inter- or intra-genic). The most frequent integration site in CC was in MACROD2 gene followed by MIPOL1/TTC6 and TP63. HPV integration signatures were not associated with histological subtype, FIGO staging, treatment or PFS. HPVs were more frequently episomal in PIK3CA mutated tumours (p = 0.023). Viral integration type was dependent on HPV genotype (p < 0.0001); HPV18 and HPV45 being always integrated. High HPV copy number was associated with longer PFS (p = 0.011).

conclusionsThis is to our knowledge the first study assessing the prognostic value of HPV integration in a prospectively annotated CC cohort, which detects a hotspot of HPV integration at MACROD2; involved in impaired PARP1 activity and chromosome instability.

Indexed as

Carcinoma, Squamous CellClass I Phosphatidylinositol 3-KinasesDNA Repair EnzymesFemaleHumansHydrolasesKallikreinsMiddle AgedPapillomaviridaePapillomavirus InfectionsProgression-Free SurvivalProstate-Specific AntigenUterine Cervical NeoplasmsVirus IntegrationClass I Phosphatidylinositol 3-KinasesDNA Repair EnzymesHydrolasesKallikreinsKLK3 protein, humanMACROD2 protein, humanPIK3CA protein, humanProstate-Specific Antigen

Identifiers

PMID33191407
PMCPMC7884736
OpenAlexW3103414128

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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.