Evidence map›Paper›PMID 37314929›Full record

ArticleCell reports2023

Breast cancer cell mesenchymal transition and metastasis directed by DAP5/eIF3d-mediated selective mRNA translation.

Amandine Alard, Olga Katsara, Tiffany Rios-Fuller, Columba de la Parra, Ugur Ozerdem, Amanda Ernlund, Robert J Schneider

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
6.5field-weighted citation impact, top 3% 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

29 citing papers in PubMed, 42 citations in OpenAlex.

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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

7 authors at 1 institution in 1 country.

Amandine AlardDepartment of Microbiology, NYU School of Medicine, New York, NY 10016, USA.
Olga KatsaraDepartment of Microbiology, NYU School of Medicine, New York, NY 10016, USA.
Tiffany Rios-FullerDepartment of Microbiology, NYU School of Medicine, New York, NY 10016, USA.
Columba de la ParraDepartment of Microbiology, NYU School of Medicine, New York, NY 10016, USA.
Ugur OzerdemDepartment of Pathology, NYU School of Medicine, New York, NY 10016, USA.
Amanda ErnlundDepartment of Microbiology, NYU School of Medicine, New York, NY 10016, USA.
Robert J SchneiderDepartment of Microbiology, NYU School of Medicine, New York, NY 10016, USA.
New York University · US

Funding

Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI MARK Reid PHILIPS · 1985 to 2026
$83.1M
Institutional Clinical and Translational Science AwardUL1TR000038 · NCATS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI CRONSTEIN, BRUCE NEIL, HOCHMAN, JUDITH S · 2012 to 2014
$16.8M
DAP5-dependent translational control and breast cancer metastasisR01CA248397 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI SCHNEIDER, ROBERT JAY · 2020 to 2024
$2.5M
Translational regulation of the breast cancer stem cell by eIF4G1R01CA178509 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI SCHNEIDER, ROBERT JAY · 2015 to 2019
$2.0M
NCATS NIH HHS UL1 TR000038NCI NIH HHS P30 CA016087NCI NIH HHS R01 CA178509NCI NIH HHS R01 CA248397
6 · The paper itself

Abstract

Cancer cell plasticity enables cell survival in harsh physiological environments and fate transitions such as the epithelial-to-mesenchymal transition (EMT) that underlies invasion and metastasis. Using genome-wide transcriptomic and translatomic studies, an alternate mechanism of cap-dependent mRNA translation by the DAP5/eIF3d complex is shown to be essential for metastasis, EMT, and tumor directed angiogenesis. DAP5/eIF3d carries out selective translation of mRNAs encoding EMT transcription factors and regulators, cell migration integrins, metalloproteinases, and cell survival and angiogenesis factors. DAP5 is overexpressed in metastatic human breast cancers associated with poor metastasis-free survival. In human and murine breast cancer animal models, DAP5 is not required for primary tumor growth but is essential for EMT, cell migration, invasion, metastasis, angiogenesis, and resistance to anoikis. Thus, cancer cell mRNA translation involves two cap-dependent mRNA translation mechanisms, eIF4E/mTORC1 and DAP5/eIF3d. These findings highlight a surprising level of plasticity in mRNA translation during cancer progression and metastasis.

Indexed as

Breast NeoplasmsEukaryotic Initiation Factor-3Eukaryotic Initiation Factor-4GProtein BiosynthesisAnimalsCell Line, TumorCell MovementEpithelial-Mesenchymal TransitionFemaleHumansMiceNeoplasm MetastasisRNA, MessengerTranscription FactorsEIF3D protein, humanEukaryotic Initiation Factor-3Eukaryotic Initiation Factor-4GRNA, MessengerTranscription Factorsbreast cancerCP: CancerCP: Molecular biologyDAP5epithelial-to-mesenchymal transitionmetastasisprotein synthesistranslation initiation

Identifiers

PMID37314929
PMCPMC10895648
OpenAlexW4380537785

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.