Evidence map›Paper›PMID 33082953›Full record

ArticleClinical & translational immunology2020

Endothelial, pericyte and tumor cell expression in glioblastoma identifies fibroblast activation protein (FAP) as an excellent target for immunotherapy.

Lisa M Ebert, Wenbo Yu, Tessa Gargett, John Toubia, Paris M Kollis, Melinda N Tea, Brenton W Ebert, Cedric Bardy, Mark van den Hurk, Claudine S Bonder and 12 more

Open access · goldAbstract read
In one paragraph

Article in Clinical & translational immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed, 3 pooled it
2.8field-weighted citation impact, top 7% 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

51 citing papers in PubMed, 3 syntheses or guidelines pooled it, 67 citations in OpenAlex.

  1. Pooled it
  2. State-of-the-art of FAPI-PET imaging: a systematic review and meta-analysis.European journal of nuclear medicine and molecular imaging · 2021
    Pooled it
  3. Pooled it
  4. Translational Theranostics in Glioblastoma: FAPI-46 as a Precision Medicine Tool.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2026
    Article
  5. FAPExperimental & molecular medicine · 2026
    Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. CD47 stabilizes ROBO2 to regulate glioblastoma progression by preventing ITCH-mediated ubiquitination.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  12. Article
  13. Article
  14. FAPαAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
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

22 authors at 5 institutions in 1 country.

Lisa M EbertCentre for Cancer Biology SA Pathology and University of South Australia Adelaide Australia.ORCID https://orcid.org/0000-0002-8041-9666
Wenbo YuCentre for Cancer Biology SA Pathology and University of South Australia Adelaide Australia.
Tessa GargettCentre for Cancer Biology SA Pathology and University of South Australia Adelaide Australia.
John ToubiaCentre for Cancer Biology SA Pathology and University of South Australia Adelaide Australia.
Paris M KollisCentre for Cancer Biology SA Pathology and University of South Australia Adelaide Australia.
Melinda N TeaCentre for Cancer Biology SA Pathology and University of South Australia Adelaide Australia.
Brenton W EbertCentre for Cancer Biology SA Pathology and University of South Australia Adelaide Australia.
Cedric BardySouth Australian Health and Medical Research Institute (SAHMRI) Adelaide Australia.
Mark van den HurkSouth Australian Health and Medical Research Institute (SAHMRI) Adelaide Australia.
Claudine S BonderCentre for Cancer Biology SA Pathology and University of South Australia Adelaide Australia.
Jim ManavisAdelaide Medical School University of Adelaide Adelaide Australia.
Kathleen S EnsbeyDepartment of Cell and Molecular Biology Sid Faithfull Brain Cancer Laboratory QIMR Berghofer Medical Research Institute Brisbane QLD Australia.
Mariana Oksdath MansillaCentre for Cancer Biology SA Pathology and University of South Australia Adelaide Australia.
Kaitlin G ScheerCentre for Cancer Biology SA Pathology and University of South Australia Adelaide Australia.
Sally L PerrinCentre for Cancer Biology SA Pathology and University of South Australia Adelaide Australia.
Rebecca J OrmsbyCollege of Medicine & Public Health Flinders University Adelaide Australia.
Santosh PoonnooseCollege of Medicine & Public Health Flinders University Adelaide Australia.
Barbara KoszycaDepartment of Anatomical Pathology SA Pathology Adelaide Australia.
Stuart M PitsonCentre for Cancer Biology SA Pathology and University of South Australia Adelaide Australia.
Bryan W DayDepartment of Cell and Molecular Biology Sid Faithfull Brain Cancer Laboratory QIMR Berghofer Medical Research Institute Brisbane QLD Australia.
Guillermo A GomezCentre for Cancer Biology SA Pathology and University of South Australia Adelaide Australia.
Michael P BrownCentre for Cancer Biology SA Pathology and University of South Australia Adelaide Australia.
South Australia Pathology · AUFlinders University · AUQIMR Berghofer Medical Research Institute · AUQueensland University of Technology · AUThe University of Adelaide · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTargeted immunotherapies such as chimeric antigen receptor (CAR)-T cells are emerging as attractive treatment options for glioblastoma, but rely on identification of a suitable tumor antigen. We validated a new target antigen for glioblastoma, fibroblast activation protein (FAP), by undertaking a detailed expression study of human samples.

methodsGlioblastoma and normal tissues were assessed using immunostaining, supported by analyses of published transcriptomic datasets. Short-term cultures of glioma neural stem (GNS) cells were compared to cultures of healthy astrocytes and neurons using flow cytometry. Glioblastoma tissues were dissociated and analysed by high-parameter flow cytometry and single-cell transcriptomics (scRNAseq).

resultsCompared to normal brain, FAP was overexpressed at the gene and protein level in a large percentage of glioblastoma tissues, with highest levels of expression associated with poorer prognosis.

conclusionFibroblast activation protein is expressed by multiple cell types within glioblastoma, highlighting it as an ideal immunotherapy antigen to target destruction of both tumor cells and their supporting vascular network.

Indexed as

blood vesselsfibroblast activation proteinglioblastomaimmunotherapyscRNAseqtarget antigen

Identifiers

PMID33082953
PMCPMC7557106
OpenAlexW3092788111

What Socratic 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 Socratic graph.