Evidence map›Paper›PMID 34131070›Full record

ArticleMolecular cancer research : MCR2021

The Prognostic Potential of Human Prostate Cancer-Associated Macrophage Subtypes as Revealed by Single-Cell Transcriptomics.

Joseph C Siefert, Bianca Cioni, Mauro J Muraro, Mohammed Alshalalfa, Judith Vivié, Henk G van der Poel, Ivo G Schoots, Elise Bekers, Felix Y Feng, Lodewyk F A Wessels and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cancer research : MCR, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

23 citing papers in PubMed, 34 citations in OpenAlex.

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  19. Radiotherapy Induces Innate Immune Responses in Patients Treated for Prostate Cancers.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
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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

12 authors at 5 institutions in 2 countries.

Joseph C Siefert *Division of Oncogenomics, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
Bianca Cioni *Division of Oncogenomics, The Netherlands Cancer Institute, Amsterdam, the Netherlands.ORCID 0000-0003-2684-4255
Mauro J MuraroSingle Cell Discoveries B.V., the Netherlands.ORCID 0000-0002-6432-8609
Mohammed AlshalalfaDepartment of Radiation Oncology, UCSF Helen Diller Family Comprehensive Cancer Center, San Francisco, California.
Judith ViviéSingle Cell Discoveries B.V., the Netherlands.
Henk G van der PoelDivision of Urology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
Ivo G SchootsDepartment of Radiology and Nuclear Medicine, The Netherlands Cancer Institute, Amsterdam, the Netherlands.ORCID 0000-0002-9804-0603
Elise BekersDepartment of Pathology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
Felix Y FengDepartment of Radiation Oncology, UCSF Helen Diller Family Comprehensive Cancer Center, San Francisco, California.
Lodewyk F A WesselsDivision of Molecular Carcinogenesis, The Netherlands Cancer Institute, Amsterdam, the Netherlands. a.bergman@nki.nl l.wessels@nki.nl w.zwart@nki.nl.ORCID 0000-0002-1656-6995
Wilbert ZwartDivision of Oncogenomics, The Netherlands Cancer Institute, Amsterdam, the Netherlands. a.bergman@nki.nl l.wessels@nki.nl w.zwart@nki.nl.
Andries M BergmanDivision of Oncogenomics, The Netherlands Cancer Institute, Amsterdam, the Netherlands. a.bergman@nki.nl l.wessels@nki.nl w.zwart@nki.nl.ORCID 0000-0001-5223-2549
Oncode Institute · NLDutch Cancer Society · NLEncontech (Netherlands) · NLUCSF Helen Diller Family Comprehensive Cancer Center · USUniversity Medical Center Utrecht · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Macrophages in the tumor microenvironment are causally linked with prostate cancer development and progression, yet little is known about their composition in neoplastic human tissue. By performing single cell transcriptomic analysis of human prostate cancer resident macrophages, three distinct populations were identified in the diseased prostate. Unexpectedly, no differences were observed between macrophages isolated from the tumorous and nontumorous portions of the prostatectomy specimens. Markers associated with canonical M1 and M2 macrophage phenotypes were identifiable, however these were not the main factors defining unique subtypes. The genes selectively associated with each macrophage cluster were used to develop a gene signature which was highly associated with both recurrence-free and metastasis-free survival. These results highlight the relevance of tissue-specific macrophage subtypes in the tumor microenvironment for prostate cancer progression and demonstrates the utility of profiling single-cell transcriptomics in human tumor samples as a strategy to design gene classifiers for patient prognostication. IMPLICATIONS: The specific macrophage subtypes present in a diseased human prostate have prognostic value, suggesting that the relative proportions of these populations are related to patient outcome. Understanding the relative contributions of these subtypes will not only inform patient prognostication, but will enable personalized immunotherapeutic strategies to increase beneficial populations or reduce detrimental populations.

Indexed as

Biomarkers, TumorGene Expression ProfilingGene Expression Regulation, NeoplasticHumansMacrophage ActivationMacrophagesMalePrognosisProstateProstatectomyProstatic NeoplasmsSingle-Cell AnalysisTranscriptomeTumor MicroenvironmentBiomarkers, Tumor

Identifiers

PMID34131070
PMCPMC9398107
OpenAlexW3172246490

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.