Evidence map›Paper›PMID 27899992›Full record

ArticleOncology letters2016

Beside P53 and PTEN: Identification of molecular alterations of the RAS/MAPK and PI3K/AKT signaling pathways in high-grade serous ovarian carcinomas to determine potential novel therapeutic targets.

Shuhui Chen, Elisa Cavazza, Catherine Barlier, Julia Salleron, Pierre Filhine-Tresarrieu, Céline Gavoilles, Jean-Louis Merlin, Alexandre Harlé

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
4.0field-weighted citation impact, top 7% 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

10 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Morphological and molecular heterogeneity of epithelial ovarian cancer: Therapeutic implications.EJC supplements : EJC : official journal of EORTC, European Organization for Research and Treatment of Cancer ... [et al.] · 2020
    Article
  8. Anti-Tumor Xanthones fromDrug design, development and therapy · 2020
    Article
  9. Article
  10. 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

8 authors at 3 institutions in 1 country.

Shuhui ChenFaculty of Pharmacy, Université de Lorraine, 54001 Nancy, France; CNRS UMR 7039 CRAN, Université de Lorraine, 54506 Vandoeuvre-les-Nancy, France; Department of Biopathology, Institut de Cancérologie de Lorraine, 54519 Vandoeuvre-les-Nancy, France; Department of Gynecological Oncology, Zhongnan Hospital, Wuhan University, Wuhan, Hubei 430071, P.R. China.
Elisa CavazzaFaculty of Pharmacy, Université de Lorraine, 54001 Nancy, France.
Catherine BarlierFaculty of Pharmacy, Université de Lorraine, 54001 Nancy, France.
Julia SalleronDepartment of Data Biostatistics, Institut de Cancérologie de Lorraine, 54519 Vandoeuvre-les-Nancy, France.
Pierre Filhine-TresarrieuFaculty of Pharmacy, Université de Lorraine, 54001 Nancy, France.
Céline GavoillesDepartment of Medical Oncology, Institut de Cancérologie de Lorraine, 54519 Vandoeuvre-les-Nancy, France.
Jean-Louis MerlinFaculty of Pharmacy, Université de Lorraine, 54001 Nancy, France; CNRS UMR 7039 CRAN, Université de Lorraine, 54506 Vandoeuvre-les-Nancy, France; Department of Biopathology, Institut de Cancérologie de Lorraine, 54519 Vandoeuvre-les-Nancy, France.
Alexandre HarléFaculty of Pharmacy, Université de Lorraine, 54001 Nancy, France; CNRS UMR 7039 CRAN, Université de Lorraine, 54506 Vandoeuvre-les-Nancy, France; Department of Biopathology, Institut de Cancérologie de Lorraine, 54519 Vandoeuvre-les-Nancy, France.
Institut de Cancérologie de Lorraine · FRCentre de Recherche en Automatique de Nancy · FRLaboratoire de Chimie Physique et Microbiologie pour l'Environnement · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite great histological and molecular heterogeneity, the clinical management of high-grade ovarian carcinomas remains unspecialized. As a major subgroup, high-grade serous ovarian carcinomas (HGSOCs) require novel therapies. In addition to utilizing conventional histological prognostic markers and performing oncogenetic investigations, the molecular diagnostic method of next generation sequencing (NGS) was performed to identify 'druggable' targets that could provide access to innovative therapy. The present study was performed in 45 HGSOC patients (mean age, 59.1 years; range, 25-87 years) with histologically proven HGSOC. Breast cancer 1/2 (

Indexed as

high-grade serous ovarian carcinomahigh resolution melting-polymerase chain reactionimmunohistochemistrynext generation sequencingsignaling pathwaytargeted therapy

Identifiers

PMID27899992
PMCPMC5103928
OpenAlexW2521717745

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.