Evidence map›Paper›PMID 24022895›Full record

ArticleStem cells (Dayton, Ohio)2014

The RNA-binding protein Musashi-1 regulates proteasome subunit expression in breast cancer- and glioma-initiating cells.

Chann Lagadec, Erina Vlashi, Patricia Frohnen, Yazeed Alhiyari, Mabel Chan, Frank Pajonk

Open access · bronzeAbstract read
In one paragraph

Article in Stem cells (Dayton, Ohio), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
3.6field-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

49 citing papers in PubMed, 81 citations in OpenAlex.

  1. The metabolic profiles of cancer stem cells.Stem cell research & therapy · 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

6 authors at 2 institutions in 1 country.

Chann LagadecDepartment of Radiation Oncology, David Geffen School of Medicine and, University of California Los Angeles, California, USA.
Erina Vlashi
Patricia Frohnen
Yazeed Alhiyari
Mabel Chan
Frank Pajonk
University of California, Los Angeles · USUniversity of Colorado Denver · US

Funding

Women's CancersP30CA016042 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Samuel Wheeler French · 1985 to 2026
$134.5M
Erythropoietin and Breast Cancer Stem CellsR01CA161294 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI PAJONK, FRANK · 2012 to 2016
$1.6M
The 26S Proteasome in Cancer Stem CellsR01CA137110 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI PAJONK, FRANK · 2009 to 2013
$1.6M
NCI NIH HHS 1R01CA161294NCI NIH HHS P30 CA016042NCI NIH HHS R01 CA137110NCI NIH HHS R01CA137110NCI NIH HHS R01 CA161294
6 · The paper itself

Abstract

Cancer stem cells (CSCs) or tumor-initiating cells, similar to normal tissue stem cells, rely on developmental pathways, such as the Notch pathway, to maintain their stem cell state. One of the regulators of the Notch pathway is Musashi-1, a mRNA-binding protein. Musashi-1 promotes Notch signaling by binding to the mRNA of Numb, the negative regulator of Notch signaling, thus preventing its translation. CSCs have also been shown to downregulate their 26S proteasome activity in several types of solid tumors, thus making them resistant to proteasome-inhibitors used as anticancer agents in the clinic. Interestingly, the Notch pathway can be inhibited by proteasomal degradation of the Notch intracellular domain (Notch-ICD); therefore, downregulation of the 26S proteasome activity can lead to stabilization of Notch-ICD. Here, we present evidence that the downregulation of the 26S proteasome in CSCs constitutes another level of control by which Musashi-1 promotes signaling through the Notch pathway and maintenance of the stem cell phenotype of this subpopulation of cancer cells. We demonstrate that Musashi-1 mediates the downregulation of the 26S proteasome by binding to the mRNA of NF-YA, the transcriptional factor regulating 26S proteasome subunit expression, thus providing an additional route by which the degradation of Notch-ICD is prevented, and Notch signaling is sustained.

Indexed as

Breast NeoplasmsCCAAT-Binding FactorCell Growth ProcessesCell Line, TumorDown-RegulationFemaleGliomaHumansNeoplastic Stem CellsNerve Tissue ProteinsProteasome Endopeptidase ComplexRNA-Binding ProteinsRNA, MessengerRNA, Small InterferingSignal TransductionTransfectionATP dependent 26S proteaseCCAAT-Binding FactorMSI1 protein, humanNerve Tissue Proteinsnuclear factor YProteasome Endopeptidase ComplexRNA-Binding ProteinsRNA, MessengerRNA, Small InterferingBreast cancer stem cellsGlioma stem cellsMusashiNF-YNotchProteasome

Identifiers

PMID24022895
PMCPMC3968686
OpenAlexW1492126200

What OpenQuestion holds

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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.