Evidence map›Paper›PMID 30575334›Full record

ArticleCancer medicine2019

LRP8 is overexpressed in estrogen-negative breast cancers and a potential target for these tumors.

Virginie Maire, Faisal Mahmood, Guillem Rigaill, Mengliang Ye, Amélie Brisson, Fariba Némati, David Gentien, Gordon C Tucker, Sergio Roman-Roman, Thierry Dubois

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2019. 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
0.7field-weighted citation impact, top 34% 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, 21 citations in OpenAlex.

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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

10 authors at 2 institutions in 1 country.

Virginie MaireTranslational Research Department, Institut Curie, PSL Research University, Paris, France.
Faisal MahmoodTranslational Research Department, Institut Curie, PSL Research University, Paris, France.
Guillem RigaillInstitute of Plant Sciences Paris-Saclay (IPS2), UMR 9213, UMR1403, CNRS, INRA, Université Paris-Sud, Université d'Evry, Université Paris-Diderot, Sorbonne Paris-Cité, Orsay, France.
Mengliang YeTranslational Research Department, Institut Curie, PSL Research University, Paris, France.
Amélie BrissonTranslational Research Department, Institut Curie, PSL Research University, Paris, France.
Fariba NématiTranslational Research Department, Institut Curie, PSL Research University, Paris, France.
David GentienTranslational Research Department, Institut Curie, PSL Research University, Paris, France.
Gordon C TuckerCenter for Therapeutic Innovation in Oncology, Institut de Recherches SERVIER, Croissy-sur-Seine, France.
Sergio Roman-RomanTranslational Research Department, Institut Curie, PSL Research University, Paris, France.
Thierry DuboisTranslational Research Department, Institut Curie, PSL Research University, Paris, France.ORCID 0000-0003-4739-6164
Université Paris Sciences et Lettres · FRUniversité Paris-Sud · FR

Funding

Cancer Research UK
6 · The paper itself

Abstract

Triple-negative breast cancer (TNBC) is the breast cancer subtype with the worst prognosis. New treatments improving the survival of TNBC patients are, therefore, urgently required. We performed a transcriptome microarray analysis to identify new treatment targets for TNBC. We found that low-density lipoprotein receptor-related protein 8 (LRP8) was more strongly expressed in estrogen receptor-negative breast tumors, including TNBCs and those overexpressing HER2, than in luminal breast tumors and normal breast tissues. LRP8 depletion decreased cell proliferation more efficiently in estrogen receptor-negative breast cancer cell lines: TNBC and HER2 overexpressing cell lines. We next focused on TNBC cells for which targeted therapies are not available. LRP8 depletion induced an arrest of the cell cycle progression in G1 phase and programmed cell death. We also found that LRP8 is required for anchorage-independent growth in vitro, and that its depletion in vivo slowed tumor growth in a xenograft model. Our findings suggest that new approaches targeting LRP8 may constitute promising treatments for hormone-negative breast cancers, those overexpressing HER2 and TNBCs.

Indexed as

AnimalsApoptosisCell CycleCell Line, TumorCell ProliferationFemaleHumansLDL-Receptor Related ProteinsMice, NudeTriple Negative Breast NeoplasmsLDL-Receptor Related Proteinslow density lipoprotein receptor-related protein 8apoptosisHER2LRP8targeted therapytriple-negative breast cancer

Identifiers

PMID30575334
PMCPMC6346259
OpenAlexW2906212992

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.