Evidence map›Paper›PMID 36417849›Full record

ArticleCell reports2022

MYC regulates a pan-cancer network of co-expressed oncogenic splicing factors.

Laura Urbanski, Mattia Brugiolo, SungHee Park, Brittany L Angarola, Nathan K Leclair, Marina Yurieva, Phil Palmer, Sangram Keshari Sahu, Olga Anczuków

Abstract read
In one paragraph

Article in Cell reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 1 pooled it
–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

46 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  5. HnRNP C binding to invertedScience advances · 2026
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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

9 authors.

Laura UrbanskiThe Jackson Laboratory for Genomic Medicine, Farmington, CT, USA; Graduate Program in Genetics and Development, UConn Health, Farmington, CT, USA.
Mattia BrugioloThe Jackson Laboratory for Genomic Medicine, Farmington, CT, USA.
SungHee ParkThe Jackson Laboratory for Genomic Medicine, Farmington, CT, USA.
Brittany L AngarolaThe Jackson Laboratory for Genomic Medicine, Farmington, CT, USA.
Nathan K LeclairThe Jackson Laboratory for Genomic Medicine, Farmington, CT, USA; Graduate Program in Genetics and Development, UConn Health, Farmington, CT, USA.
Marina YurievaThe Jackson Laboratory for Genomic Medicine, Farmington, CT, USA.
Phil PalmerLifebit, London, UK.
Sangram Keshari SahuLifebit, London, UK.
Olga AnczukówThe Jackson Laboratory for Genomic Medicine, Farmington, CT, USA; Department of Genetics and Genome Sciences, UConn Health, Farmington, CT, USA. Electronic address: olga.anczukow@jax.org.

Funding

Shared Resource ManagementP30CA034196 · NCI · JACKSON LABORATORY · PI William Carl Skarnes · 1985 to 2026
$61.9M
MYC-regulated RNA Binding Protein Networks and Spliced Isoforms Driving CancerR01CA248317 · NCI · JACKSON LABORATORY · PI ANCZUKOW-CAMARDA, OLGA · 2021 to 2025
$2.7M
Mechanisms of post-transcriptional regulation of splicing factorsR01GM138541 · NIGMS · JACKSON LABORATORY · PI ANCZUKOW-CAMARDA, OLGA · 2020 to 2024
$2.1M
Training Program in Precision Genetics of Aging, Alzheimer's Disease and Related DementiasT32AG062409 · NIA · JACKSON LABORATORY · PI Gareth R Howell, KRISTEN M O'CONNELL · 2020 to 2026
$1.5M
Role of Splicing Factors in Breast CancerR00CA178206 · NCI · JACKSON LABORATORY · PI ANCZUKOW-CAMARDA, OLGA · 2016 to 2018
$747k
NCI NIH HHS P30 CA034196NCI NIH HHS R00 CA178206NCI NIH HHS R01 CA248317NIA NIH HHS T32 AG062409NIGMS NIH HHS R01 GM138541
6 · The paper itself

Abstract

MYC is dysregulated in >50% of cancers, but direct targeting of MYC has been clinically unsuccessful. Targeting downstream MYC effector pathways represents an attractive alternative. MYC regulates alternative mRNA splicing, but the mechanistic links between MYC and the splicing machinery in cancer remain underexplored. Here, we identify a network of co-expressed splicing factors (SF-modules) in MYC-active breast tumors. Of these, one is a pan-cancer SF-module correlating with MYC activity across 33 tumor types. In mammary cell models, MYC activation leads to co-upregulation of pan-cancer module SFs and to changes in >4,000 splicing events. In breast cancer organoids, co-overexpression of the pan-cancer SF-module induces MYC-regulated splicing events and increases organoid size and invasiveness, while knockdown decreases organoid size. Finally, we uncover a MYC-activity pan-cancer splicing signature correlating with survival across tumor types. Our findings provide insight into the mechanisms of MYC-regulated splicing and for the development of therapeutics for MYC-driven tumors.

Indexed as

Breast NeoplasmsOncogenesCarcinogenesisFemaleHumansProto-Oncogene Proteins c-mycRNA SplicingRNA Splicing FactorsProto-Oncogene Proteins c-mycRNA Splicing Factorsalternative splicingbreast cancercancerco-expression analysisco-expression modulesCP: CancerMYConcogenesorganoidspan-cancerRNA splicingsplicing factorsSR proteins

Identifiers

PMID36417849
PMCPMC9731204

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.