Evidence map›Paper›PMID 32717819›Full record

ReviewInternational journal of molecular sciences2020

Tumor-Associated Macrophages in Osteosarcoma: From Mechanisms to Therapy.

Francesca Cersosimo, Silvia Lonardi, Giulia Bernardini, Brian Telfer, Giulio Eugenio Mandelli, Annalisa Santucci, William Vermi, Emanuele Giurisato

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 199 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
199citing papers in PubMed, 5 pooled it
11.0field-weighted citation impact, top 1% 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

199 citing papers in PubMed, 5 syntheses or guidelines pooled it, 271 citations in OpenAlex.

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139 more citing papers are in PubMed but not listed here.

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

8 authors at 4 institutions in 3 countries.

Francesca CersosimoDepartment of Biotechnology Chemistry and Pharmacy, University of Siena, 53100 Siena, Italy.
Silvia LonardiDepartment of Molecular and Translational Medicine, University of Brescia, 25123 Brescia, Italy.
Giulia BernardiniDepartment of Biotechnology Chemistry and Pharmacy, University of Siena, 53100 Siena, Italy.ORCID 0000-0003-0016-0728
Brian TelferDivision of Pharmacy and Optometry, School of Health Sciences, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester M13 9PL, UK.ORCID 0000-0003-1857-5120
Giulio Eugenio MandelliDepartment of Molecular and Translational Medicine, University of Brescia, 25123 Brescia, Italy.
Annalisa SantucciDepartment of Biotechnology Chemistry and Pharmacy, University of Siena, 53100 Siena, Italy.
William VermiDepartment of Molecular and Translational Medicine, University of Brescia, 25123 Brescia, Italy.ORCID 0000-0002-2291-2997
Emanuele GiurisatoDepartment of Biotechnology Chemistry and Pharmacy, University of Siena, 53100 Siena, Italy.ORCID 0000-0003-0598-6449
University of Siena · ITUniversity of Brescia · ITUniversity of Manchester · GBWashington University in St. Louis · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteosarcomas (OSs) are bone tumors most commonly found in pediatric and adolescent patients characterized by high risk of metastatic progression and recurrence after therapy. Effective therapeutic management of this disease still remains elusive as evidenced by poor patient survival rates. To achieve a more effective therapeutic management regimen, and hence patient survival, there is a need to identify more focused targeted therapies for OSs treatment in the clinical setting. The role of the OS tumor stroma microenvironment plays a significant part in the development and dissemination of this disease. Important components, and hence potential targets for treatment, are the tumor-infiltrating macrophages that are known to orchestrate many aspects of OS stromal signaling and disease progression. In particular, increased infiltration of M2-like tumor-associated macrophages (TAMs) has been associated with OS metastasis and poor patient prognosis despite currently used aggressive therapies regimens. This review aims to provide a summary update of current macrophage-centered knowledge and to discuss the possible roles that macrophages play in the process of OS metastasis development focusing on the potential influence of stromal cross-talk signaling between TAMs, cancer-stem cells and additional OSs tumoral microenvironment factors.

Indexed as

Bone NeoplasmsOsteosarcomaTumor-Associated MacrophagesHumansNeoplasm MetastasisSignal TransductionTumor Microenvironmentcancer-stem cellsmesenchymal stem cellsmetastasisosteosarcomas (OSs)therapytumor-associated macrophages (TAMs)tumor microenvironment

Identifiers

PMID32717819
PMCPMC7432207
OpenAlexW3045264243

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.