Evidence map›Paper›PMID 17420285›Full record

ArticleBlood2007

RNAi screen identifies UBE2D3 as a mediator of all-trans retinoic acid-induced cell growth arrest in human acute promyelocytic NB4 cells.

Hidenori Hattori, Xueqing Zhang, Yonghui Jia, Kulandayan K Subramanian, Hakryul Jo, Fabien Loison, Peter E Newburger, Hongbo R Luo

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

24 citing papers in PubMed, 52 citations in OpenAlex.

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  19. Retinoids regulate stem cell differentiation.Journal of cellular physiology · 2011
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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

8 authors at 3 institutions in 1 country.

Hidenori Hattori
Xueqing Zhang
Yonghui Jia
Kulandayan K Subramanian
Hakryul Jo
Fabien Loison
Peter E Newburger
Hongbo R Luo
Boston Children's Hospital · USHarvard University · USUniversity of Massachusetts Chan Medical School · US

Funding

HOX cluster intergenic non-coding RNAs in myeloid differentiation and functionR01DK054369 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI NEWBURGER, PETER E, WEISSMAN, SHERMAN MORTON · 1999 to 2013
$7.2M
Molecular basis of neutrophil spontaneous deathR01HL085100 · NHLBI · BOSTON CHILDREN'S HOSPITAL · PI LUO, HONGBO R · 2007 to 2010
$2.0M
Signal transduction in neutrophil chemotaxisR01GM076084 · NIGMS · BOSTON CHILDREN'S HOSPITAL · PI LUO, HONGBO R · 2006 to 2010
$1.5M
InsP7 in glutamate excitotoxicityR21NS052200 · NINDS · CHILDREN'S HOSPITAL BOSTON · PI LUO, HONGBO R · 2005 to 2006
$424k
NHLBI NIH HHS HL085100NHLBI NIH HHS R01 HL085100NIDDK NIH HHS DK054369NIDDK NIH HHS R01 DK054369NIGMS NIH HHS GM076084NIGMS NIH HHS R01 GM076084NINDS NIH HHS NS052200NINDS NIH HHS R21 NS052200
6 · The paper itself

Abstract

All-trans retinoic acid (ATRA) has been widely used in differentiation therapy for acute promyelocytic leukemia (APL). ATRA binds to retinoic acid receptor (RAR) and triggers the formation of the transcription coactivator complex, which leads to changes in gene expression, APL cell-cycle arrest and differentiation, and clinical remission. The mechanisms responsible for ATRA's beneficial effects are still ill-defined. Here, we conducted a large-scale, unbiased short hairpin RNA (shRNA) screen aiming to identify mediators of ATRA-induced differentiation and growth arrest of APL cells. Twenty-six proteins were identified. They cover a wide range of cellular functions, including gene expression, intracellular signaling, cell death control, stress responses, and metabolic regulation, indicating the complexity of ATRA-induced cell growth control and differentiation in APL. One of these proteins, the ubiquitin-conjugating enzyme UBE2D3, is up-regulated in ATRA-treated acute promyelocytic NB4 cells. UBE2D3 is physically associated with cyclin D1 and mediates ATRA-induced cyclin D1 degradation. Knocking down UBE2D3 by RNA interference (RNAi) leads to blockage of ATRA-induced cyclin D1 degradation and cell-cycle arrest. Thus, our results highlight the involvement of the ubiquitin-mediated proteolysis pathway in ATRA-induced cell-cycle arrest and provide a novel strategy for modulating ATRA-elicited cellular effects.

Indexed as

RNA InterferenceCell CycleCell DivisionCell Line, TumorDrug Resistance, NeoplasmHumansLeukemia, Promyelocytic, AcuteOligonucleotide Array Sequence AnalysisRNA, Small InterferingSignal TransductionTretinoinUbiquitin-Conjugating EnzymesRNA, Small InterferingTretinoinUBE2D3 protein, humanUbiquitin-Conjugating Enzymes

Identifiers

PMID17420285
PMCPMC1924478
OpenAlexW2108499089

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.