Evidence map›Paper›PMID 32850302›Full record

ReviewFrontiers in oncology2020

Contribution of the Low-Density Lipoprotein Receptor Family to Breast Cancer Progression.

Océane Campion, Tesnim Al Khalifa, Benoit Langlois, Jessica Thevenard-Devy, Stéphanie Salesse, Katia Savary, Christophe Schneider, Nicolas Etique, Stéphane Dedieu, Jérôme Devy

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 21% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

  1. Pooled it
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  10. The tangled web of dyslipidemia and cancer: Is there any association?Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences · 2022
    Review
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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 3 institutions in 1 country.

Océane CampionUniversité de Reims Champagne-Ardenne (URCA), Reims, France.
Tesnim Al KhalifaUniversité de Reims Champagne-Ardenne (URCA), Reims, France.
Benoit LangloisUniversité de Reims Champagne-Ardenne (URCA), Reims, France.
Jessica Thevenard-DevyUniversité de Reims Champagne-Ardenne (URCA), Reims, France.
Stéphanie SalesseUniversité de Reims Champagne-Ardenne (URCA), Reims, France.
Katia SavaryUniversité de Reims Champagne-Ardenne (URCA), Reims, France.
Christophe SchneiderUniversité de Reims Champagne-Ardenne (URCA), Reims, France.
Nicolas EtiqueUniversité de Reims Champagne-Ardenne (URCA), Reims, France.
Stéphane DedieuUniversité de Reims Champagne-Ardenne (URCA), Reims, France.
Jérôme DevyUniversité de Reims Champagne-Ardenne (URCA), Reims, France.
Matrice Extracellulaire et Dynamique Cellulaire MEDyCUniversité de Reims Champagne-Ardenne · FRCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The low-density lipoprotein receptor (LDLR) family comprises 14 single-transmembrane receptors sharing structural homology and common repeats. These receptors specifically recognize and internalize various extracellular ligands either alone or complexed with membrane-spanning co-receptors that are then sorted for lysosomal degradation or cell-surface recovery. As multifunctional endocytic receptors, some LDLR members from the core family were first considered as potential tumor suppressors due to their clearance activity against extracellular matrix-degrading enzymes. LDLRs are also involved in pleiotropic functions including growth factor signaling, matricellular proteins, and cell matrix adhesion turnover and chemoattraction, thereby affecting both tumor cells and their surrounding microenvironment. Therefore, their roles could appear controversial and dependent on the malignancy state. In this review, recent advances highlighting the contribution of LDLR members to breast cancer progression are discussed with focus on (1) specific expression patterns of these receptors in primary cancers or distant metastasis and (2) emerging mechanisms and signaling pathways. In addition, potential diagnosis and therapeutic options are proposed.

Indexed as

biomarkerbreast cancerLDLRmicroenvironmenttherapeutic targets

Identifiers

PMID32850302
PMCPMC7406569
OpenAlexW3046382081

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.