Evidence map›Paper›PMID 30709931›Full record

ArticleCancer research2019

Landscape of Germline and Somatic Mitochondrial DNA Mutations in Pediatric Malignancies.

Petr Triska, Kristiyana Kaneva, Daria Merkurjev, Noor Sohail, Marni J Falk, Timothy J Triche, Jaclyn A Biegel, Xiaowu Gai

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

34 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Review
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  6. Review
  7. Review
  8. Pediatric Chordoma: A Tale of Two Genomes.Molecular cancer research : MCR · 2024
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Mitochondrial DNA mutations in Medulloblastoma.Acta neuropathologica communications · 2023
    Article
  15. Review
  16. Article
  17. Review
  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

8 authors at 4 institutions in 1 country.

Petr TriskaCenter for Personalized Medicine, Department of Pathology and Laboratory Medicine, Children's Hospital Los Angeles, Los Angeles, California.
Kristiyana KanevaCenter for Personalized Medicine, Department of Pathology and Laboratory Medicine, Children's Hospital Los Angeles, Los Angeles, California.
Daria MerkurjevCenter for Personalized Medicine, Department of Pathology and Laboratory Medicine, Children's Hospital Los Angeles, Los Angeles, California.
Noor SohailCenter for Epigenetics, Van Andel Research Institute, Grand Rapids, Michigan.
Marni J FalkUniversity of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania.
Timothy J TricheCenter for Epigenetics, Van Andel Research Institute, Grand Rapids, Michigan.
Jaclyn A BiegelCenter for Personalized Medicine, Department of Pathology and Laboratory Medicine, Children's Hospital Los Angeles, Los Angeles, California. xgai@chla.usc.edu jbiegel@chla.usc.edu.
Xiaowu GaiCenter for Personalized Medicine, Department of Pathology and Laboratory Medicine, Children's Hospital Los Angeles, Los Angeles, California. xgai@chla.usc.edu jbiegel@chla.usc.edu.
University of Southern California · USVan Andel Institute · USChildren's Hospital of Los Angeles · USChildren's Hospital of Philadelphia · US

Funding

Resource ProjectU41HG006834 · NHGRI · BRIGHAM AND WOMEN'S HOSPITAL · PI REHM, HEIDI L · 2013 to 2020
$26.9M
The North American Mitochondrial Disease Consortium (NAMDC)U54NS078059 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI HIRANO, MICHIO · 2011 to 2023
$17.5M
Training Physician Scientists in Pediatric OncologyT32CA009659 · NCI · CHILDREN'S HOSPITAL OF LOS ANGELES · PI DECLERCK, YVES A · 1991 to 2020
$2.2M
Primary Mitochondrial Disease Expert Curation PanelU24HD093483 · NICHD · CHILDREN'S HOSP OF PHILADELPHIA · PI FALK, MARNI J, GAI, XIAOWU · 2017 to 2023
$2.2M
NCI NIH HHS T32 CA009659NHGRI NIH HHS U41 HG006834NICHD NIH HHS U24 HD093483NINDS NIH HHS U54 NS078059
6 · The paper itself

Abstract

Little is known about the spectrum of mitochondrial DNA (mtDNA) mutations across pediatric malignancies. In this study, we analyzed matched tumor and normal whole genome sequencing data from 616 pediatric patients with hematopoietic malignancies, solid tumors, and brain tumors. We identified 391 mtDNA mutations in 284 tumors including 45 loss-of-function mutations, which clustered at four statistically significant hotspots in

Indexed as

MutationCase-Control StudiesChildDNA, MitochondrialFemaleGenome, MitochondrialHumansMaleNeoplasmsDNA, Mitochondrial

Identifiers

PMID30709931
PMCPMC6445760
OpenAlexW2911313027

What OpenQuestion holds

Textmetadata
LicenceTDM
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.