Evidence map›Paper›PMID 31160587›Full record

ArticleNature communications2019

Tumour-associated macrophages exhibit anti-tumoural properties in Sonic Hedgehog medulloblastoma.

Victor Maximov, Zhihong Chen, Yun Wei, M Hope Robinson, Cameron J Herting, Nithya S Shanmugam, Vasilisa A Rudneva, Kelly C Goldsmith, Tobey J MacDonald, Paul A Northcott and 2 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed
8.8field-weighted citation impact, top 2% 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

78 citing papers in PubMed, 106 citations in OpenAlex.

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18 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

12 authors at 2 institutions in 1 country.

Victor MaximovDepartment of Pediatrics, Neuro-Oncology Division and Aflac Cancer and Blood Disorders Center of Children's Healthcare of Atlanta, Emory University, Atlanta, 30322, GA, United States.
Zhihong ChenDepartment of Pediatrics, Neuro-Oncology Division and Aflac Cancer and Blood Disorders Center of Children's Healthcare of Atlanta, Emory University, Atlanta, 30322, GA, United States.
Yun WeiDepartment of Pediatrics, Neuro-Oncology Division and Aflac Cancer and Blood Disorders Center of Children's Healthcare of Atlanta, Emory University, Atlanta, 30322, GA, United States.
M Hope RobinsonDepartment of Pediatrics, Neuro-Oncology Division and Aflac Cancer and Blood Disorders Center of Children's Healthcare of Atlanta, Emory University, Atlanta, 30322, GA, United States.
Cameron J HertingDepartment of Pediatrics, Neuro-Oncology Division and Aflac Cancer and Blood Disorders Center of Children's Healthcare of Atlanta, Emory University, Atlanta, 30322, GA, United States.
Nithya S ShanmugamDepartment of Pediatrics, Neuro-Oncology Division and Aflac Cancer and Blood Disorders Center of Children's Healthcare of Atlanta, Emory University, Atlanta, 30322, GA, United States.
Vasilisa A RudnevaSt. Jude Children's Research Hospital, Memphis, 38105, TN, USA.ORCID http://orcid.org/0000-0002-4340-9311
Kelly C GoldsmithDepartment of Pediatrics, Neuro-Oncology Division and Aflac Cancer and Blood Disorders Center of Children's Healthcare of Atlanta, Emory University, Atlanta, 30322, GA, United States.
Tobey J MacDonaldDepartment of Pediatrics, Neuro-Oncology Division and Aflac Cancer and Blood Disorders Center of Children's Healthcare of Atlanta, Emory University, Atlanta, 30322, GA, United States.
Paul A NorthcottSt. Jude Children's Research Hospital, Memphis, 38105, TN, USA.
Dolores HambardzumyanDepartment of Pediatrics, Neuro-Oncology Division and Aflac Cancer and Blood Disorders Center of Children's Healthcare of Atlanta, Emory University, Atlanta, 30322, GA, United States.
Anna M KenneyDepartment of Pediatrics, Neuro-Oncology Division and Aflac Cancer and Blood Disorders Center of Children's Healthcare of Atlanta, Emory University, Atlanta, 30322, GA, United States. anna.kenney@emory.edu.ORCID http://orcid.org/0000-0001-8323-0618
Emory University · USSt. Jude Children's Research Hospital · US

Funding

Winship Cancer Institute Cancer Center Support GrantP30CA138292 · NCI · EMORY UNIVERSITY · PI Suresh S Ramalingam · 2009 to 2026
$47.5M
Tumor-Associated Macrophages in Vasogenic Cerebral Edema in Brain TumorsR01NS100864 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI Dolores Hambardzumyan · 2017 to 2026
$5.4M
Graduate Training in the Pharmacological StudiesT32GM008602 · NIGMS · EMORY UNIVERSITY · PI HALL, RANDY A. · 1996 to 2021
$5.1M
Sonic hedgehog:Insulin-Like Growth Factor Interactions in Proliferating Neural PrR01NS061070 · NINDS · VANDERBILT UNIVERSITY · PI KENNEY, ANNA MARIE · 2007 to 2016
$3.5M
Non-neoplastic cell types dictate gliomagenesis andU01CA160882 · NCI · EMORY UNIVERSITY · PI HAMBARDZUMYAN, DOLORES, HOLLAND, ERIC C. · 2012 to 2016
$2.8M
c-Myc, growth factor and breast cancerR01CA100864 · NCI · WAYNE STATE UNIVERSITY · PI LIAO, DEZHONG JOSHUA · 2003 to 2007
$1.6M
The Role of IL-1 in Glioblastoma-Associated Angiogenesis and Tumor ProgressionF31NS106887 · NINDS · EMORY UNIVERSITY · PI HERTING, CAMERON · 2018 to 2019
$83k
NCI NIH HHS P30 CA138292NCI NIH HHS U01 CA160882NIGMS NIH HHS T32 GM008602NINDS NIH HHS F31 NS106887NINDS NIH HHS R01 NS061070NINDS NIH HHS R01 NS100864
6 · The paper itself

Abstract

Medulloblastoma, which is the most common malignant paediatric brain tumour, has a 70% survival rate, but standard treatments often lead to devastating life-long side effects and recurrence is fatal. One of the emerging strategies in the search for treatments is to determine the roles of tumour microenvironment cells in the growth and maintenance of tumours. The most attractive target is tumour-associated macrophages (TAMs), which are abundantly present in the Sonic Hedgehog (SHH) subgroup of medulloblastoma. Here, we report an unexpected beneficial role of TAMs in SHH medulloblastoma. In human patients, decreased macrophage number is correlated with significantly poorer outcome. We confirm macrophage anti-tumoural behaviour in both ex vivo and in vivo murine models of SHH medulloblastoma. Taken together, our findings suggest that macrophages play a positive role by impairing tumour growth in medulloblastoma, in contrast to the pro-tumoural role played by TAMs in glioblastoma, another common brain tumour.

Indexed as

AnimalsAntigens, CDAntigens, Differentiation, MyelomonocyticCalcium-Binding ProteinsCD11b AntigenCD68 MoleculeCerebellar NeoplasmsChemokine CCL2Disease Models, AnimalDNA-Binding ProteinsHedgehog ProteinsHumansMacrophagesMedulloblastomaMiceMicrofilament ProteinsAIF1 protein, humanAntigens, CDAntigens, Differentiation, MyelomonocyticCalcium-Binding ProteinsCcr2 protein, mouseCD11b AntigenCD68 antigen, humanCD68 MoleculeChemokine CCL2DNA-Binding ProteinsHedgehog ProteinsITGAM protein, humanMicrofilament ProteinsReceptors, CCR2

Identifiers

PMID31160587
PMCPMC6546707
OpenAlexW2948584774

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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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.