Evidence map›Paper›PMID 34188192›Full record

ReviewNature reviews. Cancer2021

MYC protein interactors in gene transcription and cancer.

Corey Lourenco, Diana Resetca, Cornelia Redel, Peter Lin, Alannah S MacDonald, Roberto Ciaccio, Tristan M G Kenney, Yong Wei, David W Andrews, Maria Sunnerhagen and 3 more

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 204 papers.

0numbers the graph read from it
0cells of the map it votes in
204citing papers in PubMed
20.4field-weighted citation impact, top 1% 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

204 citing papers in PubMed, 334 citations in OpenAlex.

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144 more citing papers are in PubMed but not listed here.

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

13 authors at 4 institutions in 3 countries.

Corey LourencoPrincess Margaret Cancer Centre, Toronto, ON, Canada.
Diana Resetca *Princess Margaret Cancer Centre, Toronto, ON, Canada.
Cornelia Redel *Princess Margaret Cancer Centre, Toronto, ON, Canada.ORCID http://orcid.org/0000-0002-3632-3317
Peter LinPrincess Margaret Cancer Centre, Toronto, ON, Canada.ORCID http://orcid.org/0000-0003-3710-3874
Alannah S MacDonaldPrincess Margaret Cancer Centre, Toronto, ON, Canada.
Roberto CiaccioDepartment of Pharmacy and Biotechnology, University of Bologna, Bologna, Italy.ORCID http://orcid.org/0000-0003-3024-9205
Tristan M G KenneyPrincess Margaret Cancer Centre, Toronto, ON, Canada.ORCID http://orcid.org/0000-0001-8242-4349
Yong WeiPrincess Margaret Cancer Centre, Toronto, ON, Canada.
David W AndrewsDepartment of Medical Biophysics, University of Toronto, Toronto, ON, Canada.
Maria SunnerhagenDepartment of Physics, Chemistry and Biology, Linköping University, Linköping, Sweden.
Cheryl H ArrowsmithPrincess Margaret Cancer Centre, Toronto, ON, Canada.ORCID http://orcid.org/0000-0002-4971-3250
Brian RaughtPrincess Margaret Cancer Centre, Toronto, ON, Canada.
Linda Z PennPrincess Margaret Cancer Centre, Toronto, ON, Canada. linda.penn@uhnresearch.ca.ORCID http://orcid.org/0000-0001-8133-5459
University of Toronto · CAPrincess Margaret Cancer Centre · CALinköping University · SEUniversity of Bologna · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The transcription factor and oncoprotein MYC is a potent driver of many human cancers and can regulate numerous biological activities that contribute to tumorigenesis. How a single transcription factor can regulate such a diverse set of biological programmes is central to the understanding of MYC function in cancer. In this Perspective, we highlight how multiple proteins that interact with MYC enable MYC to regulate several central control points of gene transcription. These include promoter binding, epigenetic modifications, initiation, elongation and post-transcriptional processes. Evidence shows that a combination of multiple protein interactions enables MYC to function as a potent oncoprotein, working together in a 'coalition model', as presented here. Moreover, as MYC depends on its protein interactome for function, we discuss recent research that emphasizes an unprecedented opportunity to target protein interactors to directly impede MYC oncogenesis.

Indexed as

Transcription, GeneticAnimalsGene Expression Regulation, NeoplasticHumansNeoplasmsOncogene Protein p55(v-myc)Transcription FactorsOncogene Protein p55(v-myc)Transcription Factors

Identifiers

PMID34188192
OpenAlexW3173153622

What OpenQuestion holds

Textmetadata
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.