Evidence map›Paper›PMID 31547627›Full record

ReviewInternational journal of molecular sciences2019

Latest Advances in Targeting the Tumor Microenvironment for Tumor Suppression.

Chloé Laplagne, Marcin Domagala, Augustin Le Naour, Christophe Quemerais, Dimitri Hamel, Jean-Jacques Fournié, Bettina Couderc, Corinne Bousquet, Audrey Ferrand, Mary Poupot

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
–field-weighted citation impact
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

38 citing papers in PubMed.

  1. Review
  2. Effect of clinically relevant iron oxide nanoparticles on macrophage polarization, tumor growth and tumor microenvironment modulation.Journal of controlled release : official journal of the Controlled Release Society · 2026
    Article
  3. Article
  4. Role of Exosomal Non-Coding RNAsMicroRNA (Shariqah, United Arab Emirates) · 2026
    Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Heme: The Lord of the Iron Ring.Antioxidants (Basel, Switzerland) · 2023
    Review
  16. Article
  17. Article
  18. Review
  19. Review
  20. Review
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.

Chloé LaplagneCentre de Recherches en Cancérologie de Toulouse, Inserm UMR1037, 31037 Toulouse, France. chloe.laplagne@inserm.fr.
Marcin DomagalaCentre de Recherches en Cancérologie de Toulouse, Inserm UMR1037, 31037 Toulouse, France. marcin.domagala@inserm.fr.
Augustin Le NaourCentre de Recherches en Cancérologie de Toulouse, Inserm UMR1037, 31037 Toulouse, France. augustin.lenaour@inserm.fr.
Christophe QuemeraisCentre de Recherches en Cancérologie de Toulouse, Inserm UMR1037, 31037 Toulouse, France. christophe.quemerais@inserm.fr.
Dimitri HamelUniversité Toulouse III Paul-Sabatier, 31400 Toulouse, France. dimitri.hamel@inserm.fr.
Jean-Jacques FourniéCentre de Recherches en Cancérologie de Toulouse, Inserm UMR1037, 31037 Toulouse, France. jean-jacques.fournie@inserm.fr.
Bettina CoudercCentre de Recherches en Cancérologie de Toulouse, Inserm UMR1037, 31037 Toulouse, France. bettina.couderc@inserm.fr.ORCID 0000-0002-4530-5508
Corinne BousquetCentre de Recherches en Cancérologie de Toulouse, Inserm UMR1037, 31037 Toulouse, France. corinne.bousquet@inserm.fr.ORCID 0000-0002-2501-0593
Audrey FerrandUniversité Toulouse III Paul-Sabatier, 31400 Toulouse, France. audrey.ferrand@inserm.fr.
Mary PoupotCentre de Recherches en Cancérologie de Toulouse, Inserm UMR1037, 31037 Toulouse, France. mary.poupot@inserm.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The tumor bulk is composed of a highly heterogeneous population of cancer cells, as well as a large variety of resident and infiltrating host cells, extracellular matrix proteins, and secreted proteins, collectively known as the tumor microenvironment (TME). The TME is essential for driving tumor development by promoting cancer cell survival, migration, metastasis, chemoresistance, and the ability to evade the immune system responses. Therapeutically targeting tumor-associated macrophages (TAMs), cancer-associated fibroblasts (CAFs), regulatory T-cells (T-regs), and mesenchymal stromal/stem cells (MSCs) is likely to have an impact in cancer treatment. In this review, we focus on describing the normal physiological functions of each of these cell types and their behavior in the cancer setting. Relying on the specific surface markers and secreted molecules in this context, we review the potential targeting of these cells inducing their depletion, reprogramming, or differentiation, or inhibiting their pro-tumor functions or recruitment. Different approaches were developed for this targeting, namely, immunotherapies, vaccines, small interfering RNA, or small molecules.

Indexed as

ImmunotherapyNeoplasmsCancer-Associated FibroblastsCell DifferentiationHumansMesenchymal Stem CellsT-Lymphocytes, RegulatoryTumor MicroenvironmentCAFsMSCsresistanceTAMsT-regstumor microenvironment

Identifiers

PMID31547627
PMCPMC6801830

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.