Evidence map›Paper›PMID 28401258›Full record

ReviewCancer immunology, immunotherapy : CII2017

Tumor-associated myeloid cells as guiding forces of cancer cell stemness.

Antonio Sica, Chiara Porta, Alberto Amadori, Anna Pastò

Abstract readReview
In one paragraph

Review in Cancer immunology, immunotherapy : CII, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing 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

29 citing papers in PubMed.

  1. Review
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  7. Article
  8. Immune evasion by cancer stem cells.Regenerative therapy · 2021
    Review
  9. Article
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  11. Review
  12. Article
  13. Influence of Innate Immunity on Cancer Cell Stemness.International journal of molecular sciences · 2020
    Review
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  15. Review
  16. Article
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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

4 authors.

Antonio SicaDepartment of Pharmaceutical Sciences, Università del Piemonte Orientale "Amedeo Avogadro", Via Bovio 6, 28100, Novara, Italy. antonio.sica@uniupo.it.
Chiara PortaDepartment of Pharmaceutical Sciences, Università del Piemonte Orientale "Amedeo Avogadro", Via Bovio 6, 28100, Novara, Italy.
Alberto AmadoriDepartment of Surgery, Oncology and Gastroenterology, University of Padova, Padua, Italy.
Anna PastòIstituto Oncologico Veneto IOV-IRCCS, Padua, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Due to their ability to differentiate into various cell types and to support tissue regeneration, stem cells simultaneously became the holy grail of regenerative medicine and the evil obstacle in cancer therapy. Several studies have investigated niche-related conditions that favor stemness properties and increasingly emphasized their association with an inflammatory environment. Tumor-associated macrophages (TAMs) and myeloid-derived suppressor cells (MDSCs) are major orchestrators of cancer-related inflammation, able to dynamically express different polarized inflammatory programs that promote tumor outgrowth, including tumor angiogenesis, immunosuppression, tissue remodeling and metastasis formation. In addition, these myeloid populations support cancer cell stemness, favoring tumor maintenance and progression, as well as resistance to anticancer treatments. Here, we discuss inflammatory circuits and molecules expressed by TAMs and MDSCs as guiding forces of cancer cell stemness.

Indexed as

AnimalsCarcinogenesisGene Expression Regulation, NeoplasticHumansImmune ToleranceImmunotherapyInflammationMacrophagesMyeloid-Derived Suppressor CellsNeoplasmsNeoplastic Stem CellsTumor MicroenvironmentCancer stem cellsInflammationMyeloid-derived suppressor cellsRegulatory myeloid suppressor cellsTumor-associated macrophages

Identifiers

PMID28401258
PMCPMC11029054

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.