Evidence map›Paper›PMID 29854300›Full record

ArticleOncotarget2018

LRP5 regulates the expression of STK40, a new potential target in triple-negative breast cancers.

Sylvie Maubant, Tania Tahtouh, Amélie Brisson, Virginie Maire, Fariba Némati, Bruno Tesson, Mengliang Ye, Guillem Rigaill, Maïté Noizet, Aurélie Dumont and 9 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

21 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Role of PRMT1 and PRMT5 in Breast Cancer.International journal of molecular sciences · 2024
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Cancers · 2021
    Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Review
  20. 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

19 authors at 4 institutions in 1 country.

Sylvie Maubant *Institut Curie, PSL Research University, Translational Research Department, Breast Cancer Biology Group, Paris, France.
Tania Tahtouh *Institut Curie, PSL Research University, Translational Research Department, Breast Cancer Biology Group, Paris, France.
Amélie BrissonInstitut Curie, PSL Research University, Translational Research Department, Breast Cancer Biology Group, Paris, France.
Virginie MaireInstitut Curie, PSL Research University, Translational Research Department, Breast Cancer Biology Group, Paris, France.
Fariba NématiInstitut Curie, PSL Research University, Translational Research Department, Preclinical Investigation Laboratory, Paris, France.
Bruno TessonInstitut Curie, PSL Research University, Translational Research Department, Breast Cancer Biology Group, Paris, France.
Mengliang YeInstitut Curie, PSL Research University, Translational Research Department, Breast Cancer Biology Group, Paris, France.
Guillem RigaillInstitute of Plant Sciences Paris-Saclay (IPS2), UMR 9213/UMR 1403, CNRS, INRA, Université Paris-Sud, Université d'Evry, Université Paris-Diderot, Sorbonne Paris-Cité, Orsay, France.
Maïté NoizetInstitut Curie, PSL Research University, Translational Research Department, Breast Cancer Biology Group, Paris, France.
Aurélie DumontInstitut Curie, PSL Research University, Translational Research Department, Breast Cancer Biology Group, Paris, France.
David GentienInstitut Curie, PSL Research University, Translational Research Department, Genomics Platform, Paris, France.
Bérengère Marty-ProuvostInstitut Curie, PSL Research University, Translational Research Department, Breast Cancer Biology Group, Paris, France.
Leanne de KoningInstitut Curie, PSL Research University, Translational Research Department, Reverse-Phase Protein Array Platform, Paris, France.
Sardar Faisal MahmoodInstitut Curie, PSL Research University, Translational Research Department, Breast Cancer Biology Group, Paris, France.
Didier DecaudinInstitut Curie, PSL Research University, Translational Research Department, Preclinical Investigation Laboratory, Paris, France.
Francisco CruzaleguiOncology Research and Development Unit, Institut de Recherches SERVIER, Croissy-Sur-Seine, France.
Gordon C TuckerOncology Research and Development Unit, Institut de Recherches SERVIER, Croissy-Sur-Seine, France.
Sergio Roman-RomanInstitut Curie, PSL Research University, Translational Research Department, Paris, France.
Thierry DuboisInstitut Curie, PSL Research University, Translational Research Department, Breast Cancer Biology Group, Paris, France.
Université Paris Sciences et Lettres · FRInstitut Curie · FRAVL (France) · FRUniversité Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Triple-negative breast cancers (TNBCs) account for a large proportion of breast cancer deaths, due to the high rate of recurrence from residual, resistant tumor cells. New treatments are needed, to bypass chemoresistance and improve survival. The WNT pathway, which is activated in TNBCs, has been identified as an attractive pathway for treatment targeting. We analyzed expression of the WNT coreceptors LRP5 and LRP6 in human breast cancer samples. As previously described, LRP6 was overexpressed in TNBCs. However, we also showed, for the first time, that LRP5 was overexpressed in TNBCs too. The knockdown of LRP5 or LRP6 decreased tumorigenesis

Indexed as

LRP5LRP6STK40targeted therapytriple-negative breast cancer

Identifiers

PMID29854300
PMCPMC5978250
OpenAlexW2800034277

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.