Evidence map›Paper›PMID 32481735›Full record

ReviewInternational journal of molecular sciences2020

Elizabeth Santana Dos Santos, François Lallemand, Ambre Petitalot, Sandrine M Caputo, Etienne Rouleau

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2020. 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
1.5field-weighted citation impact, top 15% 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, 27 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Genomic instability andFrontiers in oncology · 2025
    Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Breast Cancer Predisposition Genes and Synthetic Lethality.International journal of molecular sciences · 2021
    Review
  15. Review
  16. Targeting DNA Damage Response in Prostate and Breast Cancer.International journal of molecular sciences · 2020
    Review
  17. BeyondJournal of clinical medicine · 2020
    Article
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

5 authors at 2 institutions in 2 countries.

Elizabeth Santana Dos SantosDepartment of Medical Biology and Pathology, Gustave Roussy, Cancer Genetics Laboratory, Gustave Roussy, 94800 Villejuif, France.ORCID 0000-0002-2038-4668
François LallemandDepartment of Genetics, Institut Curie, 75005 Paris, France.
Ambre PetitalotDepartment of Genetics, Institut Curie, 75005 Paris, France.
Sandrine M CaputoDepartment of Genetics, Institut Curie, 75005 Paris, France.ORCID 0000-0001-5338-9388
Etienne RouleauDepartment of Medical Biology and Pathology, Gustave Roussy, Cancer Genetics Laboratory, Gustave Roussy, 94800 Villejuif, France.
Université Paris Sciences et Lettres · FRInstitut Gustave Roussy · FR

Funding

French National Cancer Institute (INCa) [PRT-K14-134 to E. SdS, SC and AP], USA BCRF-16-096, 2017-2018 to AP].
6 · The paper itself

Abstract

Ovarian and breast cancers are currently defined by the main pathways involved in the tumorigenesis. The majority are carcinomas, originating from epithelial cells that are in constant division and subjected to cyclical variations of the estrogen stimulus during the female hormonal cycle, therefore being vulnerable to DNA damage. A portion of breast and ovarian carcinomas arises in the context of DNA repair defects, in which genetic instability is the backdrop for cancer initiation and progression. For these tumors, DNA repair deficiency is now increasingly recognized as a target for therapeutics. In hereditary breast/ovarian cancers (HBOC), tumors with

Indexed as

CarcinogenesisDNA DamageDNA RepairHomologous RecombinationAntineoplastic AgentsApoptosisBiomarkers, TumorBreast NeoplasmsCell CycleFemaleGenes, BRCA1Genes, BRCA2Genetic Predisposition to DiseaseGerm-Line MutationHumansMutationAntineoplastic AgentsBiomarkers, TumorBRCA1BRCA2breast cancer tumorigenesisDNA repairhereditary breast cancerhereditary ovarian cancerhomologous recombination deficiencyovarian cancer tumorigenesis

Identifiers

PMID32481735
PMCPMC7312125
OpenAlexW3030736573

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.