Evidence map›Paper›PMID 32974182›Full record

ArticleFrontiers in oncology2020

Adipose Tissue Properties in Tumor-Bearing Breasts.

Isabelle Miran, Dominique Scherer, Pauline Ostyn, Chafika Mazouni, Françoise Drusch, Marine Bernard, Emilie Louvet, Julien Adam, Marie-Christine Mathieu, Mariam Haffa and 7 more

Open access · goldAbstract read
In one paragraph

Article 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 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 26% 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

9 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Adipocytes secretome from normal and tumor breast favor breast cancer invasion by metabolic reprogramming.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
    Article
  6. Review
  7. Review
  8. Review
  9. 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

17 authors at 4 institutions in 2 countries.

Isabelle MiranTranslational Research Lab, INSERM U981, Université Paris-Saclay, Villejuif, France.
Dominique SchererDivision of Preventive Oncology, National Center for Tumor Diseases (NCT) and German Cancer Research Center (DKFZ), Heidelberg, Germany.
Pauline OstynUMR 9019 Genome Integrity and Cancers, Université Paris-Saclay, Villejuif, France.
Chafika MazouniBreast Cancer Group, Université Paris-Saclay, Villejuif, France.
Françoise DruschBiology and Pathology Department, Université Paris-Saclay, Villejuif, France.
Marine BernardBiology and Pathology Department, Université Paris-Saclay, Villejuif, France.
Emilie LouvetBiology and Pathology Department, Université Paris-Saclay, Villejuif, France.
Julien AdamBiology and Pathology Department, Université Paris-Saclay, Villejuif, France.
Marie-Christine MathieuLaboratoire d'Etude des Résidus et Contaminants dans les Aliments (LABERCA), UMR 1329 Oniris-INRA, Nantes, France.
Mariam HaffaDivision of Preventive Oncology, National Center for Tumor Diseases (NCT) and German Cancer Research Center (DKFZ), Heidelberg, Germany.
Jean-Philippe AntignacLaboratoire d'Etude des Résidus et Contaminants dans les Aliments (LABERCA), UMR 1329 Oniris-INRA, Nantes, France.
Bruno Le BizecLaboratoire d'Etude des Résidus et Contaminants dans les Aliments (LABERCA), UMR 1329 Oniris-INRA, Nantes, France.
Philippe VielhBiology and Pathology Department, Université Paris-Saclay, Villejuif, France.
Philippe DessenBioinformatics Core Facility, Université Paris-Saclay, Villejuif, France.
Hervé PerdryINSERM U669 - Equipe GGS Génomique & Génétique Statistique, Villejuif, France.
Suzette DelalogeBreast Cancer Group, Université Paris-Saclay, Villejuif, France.
Jean FeunteunUMR 9019 Genome Integrity and Cancers, Université Paris-Saclay, Villejuif, France.
Université Paris-Saclay · FRLaboratoire D'étude des Résidus et Contaminants Dans les Aliments · FRGerman Cancer Research Center · DEInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The tissue stroma plays a major role in tumors' natural history. Most programs for tumor progression are not activated as cell-autonomous processes but under the conditions of cross-talks between tumor and stroma. Adipose tissue is a major component of breast stroma. This study compares adipose tissues in tumor-bearing breasts to those in tumor-free breasts with the intention of defining a signature that could translate into markers of cancer risk. In tumor-bearing breasts, we sampled adipose tissues adjacent to, or distant from the tumor. Parameters studied included: adipocytes size and density, immune cell infiltration, vascularization, secretome and gene expression. Adipose tissues from tumor-bearing breasts, whether adjacent to or distant from the tumor, do not differ from each other by any of these parameters. By contrast, adipose tissues from tumor-bearing breasts have the capacity to secrete twice as much interleukin 8 (IL-8) than those from tumor-free breasts and differentially express a set of 137 genes of which a significant fraction belongs to inflammation, integrin and wnt signaling pathways. These observations show that adipose tissues from tumor-bearing breasts have a distinct physiological status from those from tumor-free breasts. We propose that this constitutive status contributes as a non-cell autonomous process to determine permissiveness for tumor growth.

Indexed as

adipose tissuebreast cancerIL-8non-cell autonomouspermissive cancer niche

Identifiers

PMID32974182
PMCPMC7472783
OpenAlexW3080114085

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.