Evidence map›Paper›PMID 33234576›Full record

ArticleMolecular cancer research : MCR2021

MYC Activity Inference Captures Diverse Mechanisms of Aberrant MYC Pathway Activation in Human Cancers.

Evelien Schaafsma, Yanding Zhao, Lanjing Zhang, Yong Li, Chao Cheng

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cancer research : MCR, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Biology · 2025
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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 3 institutions in 2 countries.

Evelien SchaafsmaDepartment of Molecular and Systems Biology, Dartmouth College, Hanover, New Hampshire.
Yanding ZhaoDepartment of Medicine, Baylor College of Medicine, Houston, Texas.
Lanjing ZhangDepartment of Biological Sciences, Rutgers University, Newark, New Jersey.ORCID https://orcid.org/0000-0001-5436-887X
Yong LiDepartment of Medicine, Section of Epidemiology and Population Sciences, Baylor College of Medicine, Houston, Texas.
Chao ChengDepartment of Medicine, Baylor College of Medicine, Houston, Texas. chao.cheng@bcm.edu.ORCID https://orcid.org/0000-0002-5002-3417
Baylor College of Medicine · USDartmouth College · USRutgers, The State University of New Jersey · US

Funding

IMMUNOBIOLOGY OF MYELOID AND LYMPHOID CELLST32AI007363 · NIAID · DARTMOUTH COLLEGE · PI Claudia V Jakubzick · 1990 to 2026
$9.5M
Identification of a noval oncogene using validation-based insertional mutagenesisR01CA138421 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI JACKSON, MARK W. · 2010 to 2020
$3.2M
Computational Identification of new candidate drugs for lung cancer treatmentR21CA227996 · NCI · BAYLOR COLLEGE OF MEDICINE · PI CHENG, CHAO, ONEGA, TRACY · 2019 to 2020
$397k
NCI NIH HHS R01 CA138421NCI NIH HHS R21 CA227996NIAID NIH HHS T32 AI007363
6 · The paper itself

Abstract

c-MYC (MYC) is deregulated in more than 50% of all cancers. While MYC amplification is the most common MYC-deregulating event, many other alterations can increase MYC activity. We thus systematically investigated MYC pathway activity across different tumor types. Using a logistic regression framework, we established tumor type-specific, transcriptomic-based MYC activity scores that can accurately capture MYC activity. We show that MYC activity scores reflect a variety of MYC-regulating mechanisms, including MYCL and/or MYCN amplification, MYC promoter methylation, MYC mRNA expression, lncRNA PVT1 expression, MYC mutations, and viral integrations near the MYC locus. Our MYC activity score incorporates all of these mechanisms, resulting in better prognostic predictions compared with MYC amplification status, MYC promoter methylation, and MYC mRNA expression in several cancer types. In addition, we show that tumor proliferation and immune evasion are likely contributors to this reduction in survival. Finally, we developed a MYC activity signature for liquid tumors in which MYC translocation is commonly observed, suggesting that our approach can be applied to different types of genomic alterations. In conclusion, we developed a MYC activity score that captures MYC pathway activity and is clinically relevant. IMPLICATIONS: By using cancer type-specific MYC activity profiles, we were able to assess MYC activity across many more tumor types than previously investigated. The range of different MYC-related alterations captured by our MYC activity score can be used to facilitate the application of future MYC inhibitors and aid physicians to preselect patients for targeted therapy.

Indexed as

Breast NeoplasmsGene AmplificationGene Expression ProfilingGenomicsHumansModels, GeneticNeoplasmsNeuroblastomaPrognosisProto-Oncogene Proteins c-mycSurvival AnalysisMYC protein, humanProto-Oncogene Proteins c-myc

Identifiers

PMID33234576
PMCPMC7925347
OpenAlexW3110640063

What OpenQuestion holds

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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.