Evidence map›Paper›PMID 32907837›Full record

ReviewCancer research2020

The Emerging Role of Ras Pathway Signaling in Pediatric Cancer.

Gina M Ney, Laura McKay, Carl Koschmann, Rajen Mody, Qing Li

Open access · greenAbstract readReview
In one paragraph

Review in Cancer research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

16 citing papers in PubMed, 28 citations in OpenAlex.

  1. Advances in the management of pediatric low-grade glioma.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2026
    Review
  2. Article
  3. Review
  4. Article
  5. Circulating Tumor DNA Is Prognostic in Intermediate-Risk Rhabdomyosarcoma: A Report From the Children's Oncology Group.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2023
    Article
  6. Article
  7. Review
  8. Review
  9. Article
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  11. Article
  12. Review
  13. Review
  14. Article
  15. Review
  16. Frontiers in pharmacology · 2021
    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

5 authors at 1 institution in 1 country.

Gina M Ney *Department of Pediatrics, University of Michigan, Ann Arbor, MI. lqing@med.umich.edu gdevault@med.umich.edu.ORCID 0000-0002-6530-780X
Laura McKay *Department of Pediatrics, University of Michigan, Ann Arbor, MI.
Carl KoschmannDepartment of Pediatrics, University of Michigan, Ann Arbor, MI.
Rajen ModyDepartment of Pediatrics, University of Michigan, Ann Arbor, MI.
Qing LiDepartment of Internal Medicine, University of Michigan, Ann Arbor, MI. lqing@med.umich.edu gdevault@med.umich.edu.ORCID 0000-0002-4982-1024
University of Michigan · US

Funding

Advancing Child Health Through Cellular and Molecular BiologyK12HD028820 · NICHD · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Donna M. Martin · 2002 to 2026
$9.2M
ONCOLOGY RESEARCH TRAINING GRANTT32CA009357 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Qing Li · 1987 to 2026
$8.6M
The role of ER associated degradation (ERAD) in hematopoietic stem cellsR01HL150707 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LI, QING · 2020 to 2024
$2.4M
Oncogenic Nras signaling in leukemic stem cell transformationR01HL132392 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LI, QING · 2016 to 2020
$1.9M
Targeting ATRX-Deficient Pediatric GBMK08NS099427 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KOSCHMANN, CARL J · 2017 to 2021
$811k
NCI NIH HHS T32 CA009357NHLBI NIH HHS R01 HL132392NHLBI NIH HHS R01 HL150707NICHD NIH HHS K12 HD028820NINDS NIH HHS K08 NS099427
6 · The paper itself

Abstract

As genomic sequencing has become more widely available, the high prevalence of Ras pathway mutations in pediatric diseases has begun to emerge. Germline Ras-activating mutations have been known to contribute to cancer predisposition in a group of disorders known as the RASopathies, and now large pediatric sequencing studies have identified frequent somatic Ras pathway alterations across a diverse group of pediatric malignancies. These include glial brain tumors, relapsed high-risk neuroblastoma, embryonal rhabdomyosarcoma, acute myeloid leukemia, and relapsed acute lymphoblastic leukemia, and their prognostic impact is becoming increasingly better understood. Clinically, there has been success in targeting the Ras pathway in pediatric diseases, including the use of MEK inhibitors in plexiform neurofibromas associated with neurofibromatosis type 1 and the use of Ras pathway inhibitors in low-grade gliomas. Given the importance of this pathway in pediatric cancer, it is imperative that future studies strive to better understand the functional significance of these mutations, including their role in tumor growth and treatment resistance and how they can be better targeted to improve outcomes.

Indexed as

Antineoplastic AgentsCentral Nervous System NeoplasmsHematologic NeoplasmsHumansMolecular Targeted TherapyMutationNeoplasmsNeurofibromatosis 1ras ProteinsSignal TransductionAntineoplastic Agentsras Proteins

Identifiers

PMID32907837
PMCPMC10081825
OpenAlexW3084353531

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.