Evidence map›Paper›PMID 20857481›Full record

ArticleJournal of cellular physiology2011

MYBL2, a link between proliferation and differentiation in maturing colon epithelial cells.

Michael Papetti, Leonard H Augenlicht

Abstract read
In one paragraph

Article in Journal of cellular physiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

25 citing papers in PubMed, 36 citations in OpenAlex.

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  12. Frontiers in oncology · 2021
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  20. Overexpression of ANXA1 confers independent negative prognostic impact in rectal cancers receiving concurrent chemoradiotherapy.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2014
    Article
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

2 authors at 2 institutions in 1 country.

Michael PapettiDepartment of Oncology, Albert Einstein Cancer Center, Montefiore Medical Center, Bronx, New York 10467, USA. mpapetti@montefiore.org
Leonard H Augenlicht
Albert Einstein College of Medicine · USMontefiore Medical Center · US

Funding

WORD PROCESSORP30CA013330 · NCI · YESHIVA UNIVERSITY · PI THOMAS E ROHAN · 1985 to 2026
$111.2M
MOLECULAR-NUTRIENT INTERACTIONS IN INTESTINAL CANCERU54CA100926 · NCI · MONTEFIORE MEDICAL CENTER (BRONX, NY) · PI AUGENLICHT, LEONARD H · 2003 to 2008
$9.7M
Nutritional mechanisms and intestinal tumorigenesisR01CA114265 · NCI · MONTEFIORE MEDICAL CENTER (BRONX, NY) · PI AUGENLICHT, LEONARD H · 2005 to 2009
$1.3M
Critical Role of Mybl2 in Spontaneous and Short-Chain Fatty Acid-Induced IntestinR21CA137508 · NCI · MONTEFIORE MEDICAL CENTER (BRONX, NY) · PI PAPETTI, MICHAEL JOSEPH · 2010 to 2011
$328k
FATTY ACID MODULATION OF COLON CELL TRANSFORMATIONR21CA123473 · NCI · MONTEFIORE MEDICAL CENTER (BRONX, NY) · PI AUGENLICHT, LEONARD H · 2007 to 2008
$305k
NCI NIH HHS CA114265NCI NIH HHS CA123473NCI NIH HHS P30 CA013330NCI NIH HHS R01 CA114265NCI NIH HHS R21 CA123473NCI NIH HHS R21 CA137508NCI NIH HHS U54 CA100926PHS HHS P013330
6 · The paper itself

Abstract

Multiple signals, controlling both proliferation and differentiation, must be integrated in the reprogramming of intestinal epithelial cells during maturation along the crypt-luminal axis. The v-myb family member Mybl2, a molecule implicated in the development and maintenance of the stem cell phenotype, has been suggested to play an important role in proliferation and differentiation of several cell types and is a gene we have found is commonly regulated in several systems of colon cell maturation both in vitro and in vivo. Here we show that siRNA silencing of Mybl2 in proliferating Caco-2 cells increases expression of the cell-cycle regulators cdk2, cyclin D2, and c-myc and decreases expression of cdc25B and cyclin B2 with a consequent 10% increase of cells in G2/M and a complementary 10% decrease in G1. Mybl2 occupies sequences upstream of transcriptional start sites of cyclin D2, c-myc, cyclin B2, and cdc25B and regulates reporter activity driven by upstream regions of cdk2, cyclin D2, and c-myc. These data suggest that Mybl2 plays a subtle but key role in linking specific aspects of cell-cycle progression with generation of signals for differentiation and may therefore be fundamental in commitment of intestinal epithelial cells to differentiation pathways during their maturation.

Indexed as

Cell DifferentiationBase SequenceCaco-2 CellsCell Cycle ProteinsCell ProliferationColonEpithelial CellsG2 PhaseGene Expression RegulationGene Knockdown TechniquesHumansMitosisModels, BiologicalProtein BindingRNA, MessengerRNA, Small InterferingCell Cycle ProteinsMYBL2 protein, humanRNA, MessengerRNA, Small InterferingTrans-Activators

Identifiers

PMID20857481
PMCPMC3012743
OpenAlexW2161117133

What OpenQuestion holds

Textmetadata
LicenceTDM
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.