Evidence map›Paper›PMID 33067172›Full record

ReviewTrends in cancer2021

Cancer Plasticity: The Role of mRNA Translation.

Laura J Lee, David Papadopoli, Michael Jewer, Sonia Del Rincon, Ivan Topisirovic, Mitchell G Lawrence, Lynne-Marie Postovit

Open access · bronzeAbstract readReview
In one paragraph

Review in Trends in cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

62 citing papers in PubMed, 91 citations in OpenAlex.

  1. Review
  2. Observational
  3. Article
  4. Review
  5. Filgotinib inhibits METTL3-mediated mNPJ precision oncology · 2026
    Article
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  13. Review
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  20. Review

2 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

7 authors at 4 institutions in 2 countries.

Laura J LeeDepartment of Oncology, University of Alberta, Edmonton, AB, Canada.
David PapadopoliLady Davis Institute, Gerald Bronfman Department of Oncology and Departments of Biochemistry and Experimental Medicine, McGill University, Montreal, QC, Canada.
Michael JewerDepartment of Oncology, University of Alberta, Edmonton, AB, Canada.
Sonia Del RinconLady Davis Institute, Gerald Bronfman Department of Oncology and Departments of Biochemistry and Experimental Medicine, McGill University, Montreal, QC, Canada.
Ivan TopisirovicLady Davis Institute, Gerald Bronfman Department of Oncology and Departments of Biochemistry and Experimental Medicine, McGill University, Montreal, QC, Canada. Electronic address: ivan.topisirovic@mcgill.ca.
Mitchell G LawrenceBiomedicine Discovery Institute Cancer Program, Prostate Cancer Research Group, Department of Anatomy and Developmental Biology, Monash University, Clayton, VIC 3800, Australia; Peter MacCallum Cancer Centre, Melbourne, VIC 3000, Australia; Sir Peter MacCallum Department of Oncology, The University of Melbourne, Parkville, VIC 3010, Australia. Electronic address: mitchell.lawrence@monash.edu.
Lynne-Marie PostovitDepartment of Oncology, University of Alberta, Edmonton, AB, Canada; Department of Biomedical and Molecular Sciences, Queen's University, Kingston, ON, Canada. Electronic address: l.postovit@queensu.ca.
McGill University · CAUniversity of Alberta · CAMonash University · AUQueen's University · CA

Funding

Control of Protein Synthesis by the UPS Under StressR01CA202021 · NCI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI RONAI, ZEEV A. · 2016 to 2020
$2.3M
NCI NIH HHS R01 CA202021
6 · The paper itself

Abstract

Tumor progression is associated with dedifferentiated histopathologies concomitant with cancer cell survival within a changing, and often hostile, tumor microenvironment. These processes are enabled by cellular plasticity, whereby intracellular cues and extracellular signals are integrated to enable rapid shifts in cancer cell phenotypes. Cancer cell plasticity, at least in part, fuels tumor heterogeneity and facilitates metastasis and drug resistance. Protein synthesis is frequently dysregulated in cancer, and emerging data suggest that translational reprograming collaborates with epigenetic and metabolic programs to effectuate phenotypic plasticity of neoplasia. Herein, we discuss the potential role of mRNA translation in cancer cell plasticity, highlight emerging histopathological correlates, and deliberate on how this is related to efforts to improve understanding of the complex tumor ecology.

Indexed as

Antineoplastic AgentsCell PlasticityDisease ProgressionDrug Resistance, NeoplasmEpithelial-Mesenchymal TransitionEukaryotic Initiation Factor-2Eukaryotic Initiation Factor-4FGene Expression Regulation, NeoplasticGenetic HeterogeneityHumansMutationNeoplasmsOxidative PhosphorylationProtein BiosynthesisTumor MicroenvironmentWarburg Effect, OncologicAntineoplastic AgentsEukaryotic Initiation Factor-2Eukaryotic Initiation Factor-4Fcancer plasticitymetabolismmRNA translationprotein synthesisstromal–epithelial interactionstherapy resistancetumor microenvironment

Identifiers

PMID33067172
PMCPMC8023421
OpenAlexW3093361155

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.