Evidence map›Paper›PMID 23255112›Full record

ArticleCell cycle (Georgetown, Tex.)2013

Regulation of miR106b cluster through the RB pathway: mechanism and functional targets.

Chellappagounder Thangavel, Ettickan Boopathi, Adam Ertel, Meng Lim, Sankar Addya, Paolo Fortina, Agnieszka K Witkiewicz, Erik S Knudsen

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

19 citing papers in PubMed, 20 citations in OpenAlex.

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  19. MCM7 expression is altered in rat after spinal cord injury.Journal of molecular neuroscience : MN · 2013
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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 5 institutions in 2 countries.

Chellappagounder ThangavelDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Ettickan Boopathi
Adam Ertel
Meng Lim
Sankar Addya
Paolo Fortina
Agnieszka K Witkiewicz
Erik S Knudsen
The University of Texas Southwestern Medical Center · USSidney Kimmel Cancer Center · USCalifornia University of Pennsylvania · USPhiladelphia University · USThomas Jefferson University · US

Funding

NCI NIH HHS NCI CA12934
6 · The paper itself

Abstract

The RB pathway plays a critical role in proliferation control that is commonly subverted in tumor development. However, restoration of RB pathway function can be elicited in many tumor cells by the inhibition of CDK4/6 activity that leads to dephosphorylation of RB and subsequent repression of E2F-mediated transcription. In this context, active RB/E2F complexes inhibit the expression of a critical program of coding genes that promote cell cycle progression. However, the non-coding RNA target genes downstream from RB that could be relevant for tumor biology remain obscure. Here, miRNA gene expression profiling identified the miR106b cluster as being efficiently repressed with CDK4/6 inhibition in an E2F and RB-dependent manner. Importantly, the miR106B-cluster is intragenic of MCM7, and through a series of functional studies, the basis of MCM7 regulation and concordant expression of the miRNA species within the 106b cluster was determined. Importantly, RB-mediated repression of the 106b cluster enhances the transcript levels of p21Cip1 and PTEN. These data provide a mechanistic basis for cross-talk between the RB pathway and p21 and PTEN through the regulation of the MCM7/miR106b locus.

Indexed as

Cell Cycle ProteinsCell Line, TumorCluster AnalysisCyclin-Dependent Kinase 4Cyclin-Dependent Kinase 6Cyclin-Dependent Kinase Inhibitor p21DNA-Binding ProteinsE2F Transcription FactorsHumansMCF-7 CellsMicroRNAsMinichromosome Maintenance Complex Component 7Multigene FamilyNuclear ProteinsPromoter Regions, GeneticPTEN PhosphohydrolaseCell Cycle ProteinsCyclin-Dependent Kinase 4Cyclin-Dependent Kinase 6Cyclin-Dependent Kinase Inhibitor p21DNA-Binding ProteinsE2F Transcription FactorsMCM7 protein, humanMicroRNAsMinichromosome Maintenance Complex Component 7MIRN106 microRNA, humanNuclear ProteinsPTEN PhosphohydrolaseRetinoblastoma Protein

Identifiers

PMID23255112
PMCPMC3570523
OpenAlexW2047870085

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.