Evidence map›Paper›PMID 31863639›Full record

ArticleJournal of cellular and molecular medicine2020

Optimized monoclonal antibody treatment against ELTD1 for GBM in a G55 xenograft mouse model.

Michelle Zalles, Nataliya Smith, Jadith Ziegler, Debra Saunders, Shannon Remerowski, Lincy Thomas, Rafal Gulej, Nadya Mamedova, Megan Lerner, Kar-Ming Fung and 8 more

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

19 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Structure of the GNature communications · 2025
    Article
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  10. ELTD1-An Emerging Silent Actor in Cancer Drama Play.International journal of molecular sciences · 2021
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Novel approaches to combat chemoresistance against glioblastomas.Cancer drug resistance (Alhambra, Calif.) · 2020
    Review
  17. Review
  18. Article
  19. Review
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

18 authors at 4 institutions in 3 countries.

Michelle ZallesAdvanced Magnetic Resonance Center, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.
Nataliya SmithAdvanced Magnetic Resonance Center, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.
Jadith ZieglerAdvanced Magnetic Resonance Center, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.
Debra SaundersAdvanced Magnetic Resonance Center, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.
Shannon RemerowskiAdvanced Magnetic Resonance Center, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.
Lincy ThomasAdvanced Magnetic Resonance Center, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.
Rafal GulejAdvanced Magnetic Resonance Center, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.
Nadya MamedovaAdvanced Magnetic Resonance Center, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.
Megan LernerSurgery Research Laboratory, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.
Kar-Ming FungDepartment of Pathology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.
Junho ChungDepartment of Biochemistry and Molecular Biology, Seoul National University College of Medicine, Seoul, Korea.
Kyusang HwangDepartment of Biochemistry and Molecular Biology, Seoul National University College of Medicine, Seoul, Korea.
Junyeong JinDepartment of Biochemistry and Molecular Biology, Seoul National University College of Medicine, Seoul, Korea.
Graham WileyClinical Genomics Center, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.
Chase BrownOklahoma Center for Neuroscience, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.
James BattisteStephenson Cancer Center, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.
Jonathan D WrenGenes & Human Disease, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.
Rheal A TownerAdvanced Magnetic Resonance Center, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.ORCID 0000-0001-7368-8983
Oklahoma Medical Research Foundation · USSeoul National University · KRUniversity of Oklahoma Health Sciences Center · USOklahoma State University · US

Funding

Tissue Pathology Shared ResourceP30CA225520 · NCI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI ROBERT S. MANNEL · 2018 to 2026
$27.1M
Understanding connective tissue development and disease with PDGFR-driven..... P20GM103636 · NIGMS · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI THOMPSON, LINDA F · 2013 to 2023
$26.9M
TUMOR RESISTANCE MECHANISMS TO ANTI-VEGF THERAPY IN PROSTATE CANCER (Sukyung Woo)P20GM103639 · NIGMS · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI DHANASEKARAN, DANNY N. · 2012 to 2022
$21.3M
Pre-Clinical 7T MRI for OklahomaS10OD023508 · OD · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI TOWNER, RHEAL A · 2017 to 2017
$600k
NCI NIH HHS P30 CA225520NIGMS NIH HHS P20 GM103636NIGMS NIH HHS P20 GM103639NIGMS NIH HHS P20GM103639NIH HHS S10 OD023508
6 · The paper itself

Abstract

Glioblastoma is an aggressive brain tumour found in adults, and the therapeutic approaches available have not significantly increased patient survival. Recently, we discovered that ELTD1, an angiogenic biomarker, is highly expressed in human gliomas. Polyclonal anti-ELTD1 treatments were effective in glioma pre-clinical models, however, pAb binding is potentially promiscuous. Therefore, the aim of this study was to determine the effects of an optimized monoclonal anti-ELTD1 treatment in G55 xenograft glioma models. MRI was used to assess the effects of the treatments on animal survival, tumour volumes, perfusion rates and binding specificity. Immunohistochemistry and histology were conducted to confirm and characterize microvessel density and Notch1 levels, and to locate the molecular probes. RNA-sequencing was used to analyse the effects of the mAb treatment. Our monoclonal anti-ELTD1 treatment significantly increased animal survival, reduced tumour volumes, normalized the vasculature and showed higher binding specificity within the tumour compared with both control- and polyclonal-treated mice. Notch1 positivity staining and RNA-seq results suggested that ELTD1 has the ability to interact with and interrupt Notch1 signalling. Although little is known about ELTD1, particularly about its ligand and pathways, our data suggest that our monoclonal anti-ELTD1 antibody is a promising anti-angiogenic therapeutic in glioblastomas.

Indexed as

Xenograft Model Antitumor AssaysAnimalsAntibodies, MonoclonalBrain NeoplasmsCell Line, TumorChickensGlioblastomaHumansMiceMicrovesselsReceptors, G-Protein-CoupledReceptors, NotchTumor BurdenADGRL4 protein, humanAntibodies, MonoclonalReceptors, G-Protein-CoupledReceptors, NotchangiogenesisELTD1glioblastoma (GBM)molecular-targeted MRImonoclonal antibody (mAb)MRInotchorthotopic G55 xenograft modelrelative cerebral blood flow (rCBF)

Identifiers

PMID31863639
PMCPMC6991683
OpenAlexW2995567829

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.