Evidence map›Paper›PMID 30401823›Full record

ArticleNature communications2018

Epigenetic profiling for the molecular classification of metastatic brain tumors.

Javier I J Orozco, Theo A Knijnenburg, Ayla O Manughian-Peter, Matthew P Salomon, Garni Barkhoudarian, John R Jalas, James S Wilmott, Parvinder Hothi, Xiaowen Wang, Yuki Takasumi and 9 more

Abstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
–field-weighted citation impact
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

60 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Cells · 2026
    Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Brain Tumor Stem Cells: New Perspectives.Methods in molecular biology (Clifton, N.J.) · 2025
    Review
  15. Article
  16. Article
  17. Article
  18. Review
  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

19 authors.

Javier I J OrozcoDepartment of Translational Molecular Medicine, John Wayne Cancer Institute at Providence Saint John's Health Center, Santa Monica, CA, 90404, USA.ORCID http://orcid.org/0000-0003-2585-358X
Theo A KnijnenburgInstitute for Systems Biology, Seattle, WA, 98109, USA.
Ayla O Manughian-PeterDepartment of Translational Molecular Medicine, John Wayne Cancer Institute at Providence Saint John's Health Center, Santa Monica, CA, 90404, USA.
Matthew P SalomonDepartment of Translational Molecular Medicine, John Wayne Cancer Institute at Providence Saint John's Health Center, Santa Monica, CA, 90404, USA.
Garni BarkhoudarianPacific Neuroscience Institute, John Wayne Cancer Institute at Providence Saint John's Health Center, Santa Monica, CA, 90404, USA.ORCID http://orcid.org/0000-0002-6615-7428
John R JalasDepartment of Pathology, Providence Saint John's Health Center, Santa Monica, CA, 90404, USA.
James S WilmottMelanoma Institute Australia, The University of Sydney, Sydney, NSW, 2065, Australia.
Parvinder HothiBen & Catherine Ivy Center for Advanced Brain Tumor Treatment, Swedish Neuroscience Institute, Seattle, WA, 98122, USA.
Xiaowen WangDepartment of Translational Molecular Medicine, John Wayne Cancer Institute at Providence Saint John's Health Center, Santa Monica, CA, 90404, USA.
Yuki TakasumiDepartment of Pathology, Providence Saint John's Health Center, Santa Monica, CA, 90404, USA.
Michael E BucklandDepartment of Neuropathology, Royal Prince Alfred Hospital, the Brain and Mind Centre, The University of Sydney, Camperdown, NSW, 2050, Australia.
John F ThompsonMelanoma Institute Australia, The University of Sydney, Sydney, NSW, 2065, Australia.
Georgina V LongMelanoma Institute Australia, The University of Sydney, Sydney, NSW, 2065, Australia.ORCID http://orcid.org/0000-0001-8894-3545
Charles S CobbsBen & Catherine Ivy Center for Advanced Brain Tumor Treatment, Swedish Neuroscience Institute, Seattle, WA, 98122, USA.
Ilya ShmulevichInstitute for Systems Biology, Seattle, WA, 98109, USA.
Daniel F KellyPacific Neuroscience Institute, John Wayne Cancer Institute at Providence Saint John's Health Center, Santa Monica, CA, 90404, USA.
Richard A ScolyerMelanoma Institute Australia, The University of Sydney, Sydney, NSW, 2065, Australia.
Dave S B HoonDepartment of Translational Molecular Medicine, John Wayne Cancer Institute at Providence Saint John's Health Center, Santa Monica, CA, 90404, USA.ORCID http://orcid.org/0000-0003-1915-3683
Diego M MarzeseDepartment of Translational Molecular Medicine, John Wayne Cancer Institute at Providence Saint John's Health Center, Santa Monica, CA, 90404, USA. MarzeseD@jwci.org.ORCID http://orcid.org/0000-0002-3258-8852

Funding

Tumor mutation signaturesP01CA077852 · NCI · UNIVERSITY OF WASHINGTON · PI MONNAT, RAYMOND J · 1999 to 2019
$26.0M
Integrative miRNA data analysis for clinical cancer genomicsU24CA210952 · NCI · PROVINCIAL HEALTH SERVICES AUTHORITY · PI JONES, STEVEN JOHN, SHMULEVICH, ILYA · 2016 to 2020
$2.0M
Identification of Melanoma Brain Metastasis Tumor BiomarkersR01CA167967 · NCI · SAINT JOHN'S CANCER INSTITUTE · PI HOON, DAVE S B · 2013 to 2017
$1.9M
NCI NIH HHS P01 CA077852NCI NIH HHS R01 CA167967NCI NIH HHS U24 CA210952
6 · The paper itself

Abstract

Optimal treatment of brain metastases is often hindered by limitations in diagnostic capabilities. To meet this challenge, here we profile DNA methylomes of the three most frequent types of brain metastases: melanoma, breast, and lung cancers (n = 96). Using supervised machine learning and integration of DNA methylomes from normal, primary, and metastatic tumor specimens (n = 1860), we unravel epigenetic signatures specific to each type of metastatic brain tumor and constructed a three-step DNA methylation-based classifier (BrainMETH) that categorizes brain metastases according to the tissue of origin and therapeutically relevant subtypes. BrainMETH predictions are supported by routine histopathologic evaluation. We further characterize and validate the most predictive genomic regions in a large cohort of brain tumors (n = 165) using quantitative-methylation-specific PCR. Our study highlights the importance of brain tumor-defining epigenetic alterations, which can be utilized to further develop DNA methylation profiling as a critical tool in the histomolecular stratification of patients with brain metastases.

Indexed as

DNA MethylationEpigenesis, GeneticAlgorithmsBrain NeoplasmsCutaneous Malignant MelanomaDNA, NeoplasmEpigenomicsFemaleGene Expression Regulation, NeoplasticHumansLung NeoplasmsMelanomaNeoplasm MetastasisSkin NeoplasmsSupervised Machine LearningDNA, Neoplasm

Identifiers

PMID30401823
PMCPMC6219520

What OpenQuestion holds

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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.