Evidence map›Paper›PMID 27236468›Full record

ReviewCellular and molecular life sciences : CMLS2016

A clinical and biological perspective of human myeloid-derived suppressor cells in cancer.

Christopher Shipp, Lisa Speigl, Nicole Janssen, Alexander Martens, Graham Pawelec

Abstract readReview
In one paragraph

Review in Cellular and molecular life sciences : CMLS, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
–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

34 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Here, There, and Everywhere: Myeloid-Derived Suppressor Cells in Immunology.Journal of immunology (Baltimore, Md. : 1950) · 2023
    Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Metabolic regulation in the immune response to cancer.Cancer communications (London, England) · 2021
    Review
  16. Article
  17. Article
  18. Review
  19. Imidazo[1,2-International journal of molecular sciences · 2020
    Article
  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

5 authors.

Christopher ShippSecond Department of Internal Medicine, University Hospital Tübingen, Waldhörnlestr. 22, 72072, Tübingen, Germany. christopher.shipp@uni-tuebingen.de.
Lisa SpeiglSecond Department of Internal Medicine, University Hospital Tübingen, Waldhörnlestr. 22, 72072, Tübingen, Germany.
Nicole JanssenSecond Department of Internal Medicine, University Hospital Tübingen, Waldhörnlestr. 22, 72072, Tübingen, Germany.
Alexander MartensSecond Department of Internal Medicine, University Hospital Tübingen, Waldhörnlestr. 22, 72072, Tübingen, Germany.
Graham PawelecSecond Department of Internal Medicine, University Hospital Tübingen, Waldhörnlestr. 22, 72072, Tübingen, Germany. graham.pawelec@uni-tuebingen.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Considering the large number of studies focused on myeloid-derived suppressor cells (MDSCs) to date, only a handful of well-defined relationships in human cancer have been established. The difficulty of assessing the impact of MDSCs in human cancer is partly due to the relatively small number of studies performed in humans. This is compounded in the literature by a common lack of clear indication of which species is being referred to for each characteristic described. These aspects may result in inappropriate extrapolation of animal studies to those in the human setting. This is especially the case for studies focused on investigating therapies which can be used to target MDSCs or those aimed at understanding their mechanism. Here, we attempt to rectify this by reviewing only studies on MDSC performed in humans. We survey studies which explore (1) whether MDSC levels are altered in cancer patients and if this is correlated with patient survival, (2) the so far identified mechanisms employed by MDSC to exert immune suppression, and (3) whether therapeutic agents can be used to target MDSCs by either altering their level, influencing their differentiation or inhibiting their suppressive function. Despite the fact that these studies clearly show that MDSCs are important in human cancer, the clinical employment of agents intended to target them has not yet been accomplished. We identify factors which have contributed to this and propose steps which may facilitate the translation of these therapies to the clinic in future.

Indexed as

HumansImmune SystemImmunosuppression TherapyModels, BiologicalMolecular Targeted TherapyMyeloid-Derived Suppressor CellsNeoplasmsClinicalHumanMDSCsMechanismSuppressionTargeting

Identifiers

PMID27236468
PMCPMC11108339

What OpenQuestion holds

Textmetadata
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.