Evidence map›Paper›PMID 37704607›Full record

ArticleNature communications2023

Detection of diagnostic and prognostic methylation-based signatures in liquid biopsy specimens from patients with meningiomas.

Grayson A Herrgott, James M Snyder, Ruicong She, Tathiane M Malta, Thais S Sabedot, Ian Y Lee, Jacob Pawloski, Guilherme G Podolsky-Gondim, Karam P Asmaro, Jiaqi Zhang and 25 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
8.6field-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

31 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Review
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  4. Review
  5. Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Review
  11. Liquid Biopsy: The Challenges of a Revolutionary Approach in Oncology.International journal of molecular sciences · 2025
    Review
  12. Article
  13. Malignant Meningiomas: From Diagnostics to Treatment.Diagnostics (Basel, Switzerland) · 2025
    Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Review
  20. A review on trends in development and translation of omics signatures in cancer.Computational and structural biotechnology journal · 2024
    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

35 authors at 3 institutions in 2 countries.

Grayson A HerrgottDepartment of Neurosurgery, Omics Laboratory, Hermelin Brain Tumor Center, Henry Ford Health, Detroit, MI, USA.
James M SnyderDepartment of Neurosurgery, Omics Laboratory, Hermelin Brain Tumor Center, Henry Ford Health, Detroit, MI, USA.
Ruicong SheDepartment of Public Health, Biostatistics, Henry Ford Health, Detroit, MI, USA.
Tathiane M MaltaDepartment of Neurosurgery, Omics Laboratory, Hermelin Brain Tumor Center, Henry Ford Health, Detroit, MI, USA.
Thais S SabedotDepartment of Neurosurgery, Omics Laboratory, Hermelin Brain Tumor Center, Henry Ford Health, Detroit, MI, USA.
Ian Y LeeDepartment of Neurosurgery, Omics Laboratory, Hermelin Brain Tumor Center, Henry Ford Health, Detroit, MI, USA.
Jacob PawloskiDepartment of Neurosurgery, Omics Laboratory, Hermelin Brain Tumor Center, Henry Ford Health, Detroit, MI, USA.
Guilherme G Podolsky-GondimDepartment of Neurosurgery, Ribeirao Preto Medical School, University of Sao Paulo, Ribeirao Preto, SP, Brazil.ORCID http://orcid.org/0000-0002-9608-2607
Karam P AsmaroDepartment of Neurosurgery, Omics Laboratory, Hermelin Brain Tumor Center, Henry Ford Health, Detroit, MI, USA.
Jiaqi ZhangDepartment of Public Health, Biostatistics, Henry Ford Health, Detroit, MI, USA.
Cara E CannellaDepartment of Public Health, Biostatistics, Henry Ford Health, Detroit, MI, USA.
Kevin NelsonDepartment of Neurosurgery, Omics Laboratory, Hermelin Brain Tumor Center, Henry Ford Health, Detroit, MI, USA.
Bartow ThomasDepartment of Neurosurgery, Omics Laboratory, Hermelin Brain Tumor Center, Henry Ford Health, Detroit, MI, USA.
Ana C deCarvalhoDepartment of Neurosurgery, Omics Laboratory, Hermelin Brain Tumor Center, Henry Ford Health, Detroit, MI, USA.ORCID http://orcid.org/0000-0003-1183-4548
Laura A HasselbachDepartment of Neurosurgery, Omics Laboratory, Hermelin Brain Tumor Center, Henry Ford Health, Detroit, MI, USA.
Kelly M TundoDepartment of Neurosurgery, Omics Laboratory, Hermelin Brain Tumor Center, Henry Ford Health, Detroit, MI, USA.
Rehnuma NewazDepartment of Neurosurgery, Omics Laboratory, Hermelin Brain Tumor Center, Henry Ford Health, Detroit, MI, USA.
Andrea TransouDepartment of Neurosurgery, Omics Laboratory, Hermelin Brain Tumor Center, Henry Ford Health, Detroit, MI, USA.
Natalia MorosiniDepartment of Neurosurgery, Omics Laboratory, Hermelin Brain Tumor Center, Henry Ford Health, Detroit, MI, USA.
Victor FranciscoDepartment of Neurosurgery, Omics Laboratory, Hermelin Brain Tumor Center, Henry Ford Health, Detroit, MI, USA.
Laila M PoissonDepartment of Neurosurgery, Omics Laboratory, Hermelin Brain Tumor Center, Henry Ford Health, Detroit, MI, USA.ORCID http://orcid.org/0000-0002-3409-6536
Dhananjay ChitaleDepartment of Pathology, Henry Ford Health, Detroit, MI, USA.ORCID http://orcid.org/0000-0002-4421-6431
Abir MukherjeeDepartment of Pathology, Henry Ford Health, Detroit, MI, USA.
Maritza S MosellaDepartment of Neurosurgery, Omics Laboratory, Hermelin Brain Tumor Center, Henry Ford Health, Detroit, MI, USA.
Adam M RobinDepartment of Neurosurgery, Omics Laboratory, Hermelin Brain Tumor Center, Henry Ford Health, Detroit, MI, USA.
Tobias WalbertDepartment of Neurosurgery, Omics Laboratory, Hermelin Brain Tumor Center, Henry Ford Health, Detroit, MI, USA.ORCID http://orcid.org/0000-0003-0667-8106
Mark RosenblumDepartment of Neurosurgery, Omics Laboratory, Hermelin Brain Tumor Center, Henry Ford Health, Detroit, MI, USA.
Tom MikkelsenDepartment of Neurosurgery, Omics Laboratory, Hermelin Brain Tumor Center, Henry Ford Health, Detroit, MI, USA.
Steven KalkanisDepartment of Neurosurgery, Omics Laboratory, Hermelin Brain Tumor Center, Henry Ford Health, Detroit, MI, USA.
Daniela P C TirapelliDepartment of Neurosurgery, Ribeirao Preto Medical School, University of Sao Paulo, Ribeirao Preto, SP, Brazil.
Daniel J WeisenbergerDepartment of Biochemistry and Molecular Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA, 90033, USA.ORCID http://orcid.org/0000-0001-8303-2603
Carlos G CarlottiDepartment of Neurosurgery, Ribeirao Preto Medical School, University of Sao Paulo, Ribeirao Preto, SP, Brazil.
Jack RockDepartment of Neurosurgery, Omics Laboratory, Hermelin Brain Tumor Center, Henry Ford Health, Detroit, MI, USA.
Ana Valeria CastroDepartment of Neurosurgery, Omics Laboratory, Hermelin Brain Tumor Center, Henry Ford Health, Detroit, MI, USA. acastro1@hfhs.org.ORCID http://orcid.org/0000-0003-1625-0015
Houtan NoushmehrDepartment of Neurosurgery, Omics Laboratory, Hermelin Brain Tumor Center, Henry Ford Health, Detroit, MI, USA. hnoushm1@hfhs.org.
Henry Ford Health System · USUniversidade de São Paulo · BRUniversity of Southern California · US

Funding

Circulating cell-free DNA methylation as an accurate tool for detection and clinical follow-up of gliomaR01CA270365 · NCI · HENRY FORD HEALTH SYSTEM · PI Houtan Noushmehr · 2023 to 2026
$2.3M
NCI NIH HHS R01 CA270365
6 · The paper itself

Abstract

Recurrence of meningiomas is unpredictable by current invasive methods based on surgically removed specimens. Identification of patients likely to recur using noninvasive approaches could inform treatment strategy, whether intervention or monitoring. In this study, we analyze the DNA methylation levels in blood (serum and plasma) and tissue samples from 155 meningioma patients, compared to other central nervous system tumor and non-tumor entities. We discover DNA methylation markers unique to meningiomas and use artificial intelligence to create accurate and universal models for identifying and predicting meningioma recurrence, using either blood or tissue samples. Here we show that liquid biopsy is a potential noninvasive and reliable tool for diagnosing and predicting outcomes in meningioma patients. This approach can improve personalized management strategies for these patients.

Indexed as

Meningeal NeoplasmsMeningiomaArtificial IntelligenceDNA MethylationHumansLiquid BiopsyPrognosis

Identifiers

PMID37704607
PMCPMC10499807
OpenAlexW4386698968

What OpenQuestion holds

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LicenceCC BY
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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.