Evidence map›Paper›PMID 26287603›Full record

ArticleOncotarget2015

Identification of miR-215 mediated targets/pathways via translational immunoprecipitation expression analysis (TrIP-chip).

Andrew Fesler, Xiao Xu, Xiao Zheng, Xiaodong Li, Jingting Jiang, James J Russo, Jingfang Ju

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

8 citing papers in PubMed, 9 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 4 institutions in 2 countries.

Andrew FeslerDepartment of Pathology, Stony Brook University, School of Medicine, Stony Brook, NY, USA.
Xiao XuIcahn School of Medicine at Mount Sinai, New York, NY, USA.
Xiao ZhengThe Third Affiliated Hospital, Soochow University, China.
Xiaodong LiThe Third Affiliated Hospital, Soochow University, China.
Jingting JiangThe Third Affiliated Hospital, Soochow University, China.
James J RussoCenter for Genome Technology and Biomolecular Engineering, Department of Chemical Engineering, Columbia University, New York, NY, USA.
Jingfang JuDepartment of Pathology, Stony Brook University, School of Medicine, Stony Brook, NY, USA.
Soochow University · CNStony Brook University · USIcahn School of Medicine at Mount Sinai · USNew York Genome Center · US

Funding

Molecular Mechanism of miR-140 in Colon CancerR01CA155019 · NCI · STATE UNIVERSITY NEW YORK STONY BROOK · PI JU, JINGFANG · 2011 to 2014
$1.5M
NCI NIH HHS R01 CA155019NCI NIH HHS R33CA14796603
6 · The paper itself

Abstract

Steady state mRNA expression profiling can identify the majority of miRNA targets. However, some translationally repressed miRNA targets are missed and thus not considered for functional validation. Therefore, analysis of mRNA translation can enhance miRNA target identification for functional studies. We have applied a unique approach to identify miRNA targets in a small number of cells. Actively translating mRNAs are associated with polyribosomes and newly synthesized peptide chains are associated with molecular chaperones such as HSP70s. Affinity capture beads were used to capture HSP70 chaperones associated with polyribosome complexes. The isolated actively translating mRNAs were used for high throughput expression profiling analysis. miR-215 is an important miRNA in colorectal cancer and loss of miR-215 is significantly associated with prognosis of this disease. miR-215 suppresses the expression of several key targets. We utilized the affinity capture approach to isolate miR-215 mediated mRNA target transcripts. This approach provides a unique way to identify targets regulated by non-coding RNAs and RNA binding proteins from a small number of cells.

Indexed as

Gene Expression Regulation, NeoplasticAlgorithmsColorectal NeoplasmsGene Expression ProfilingHCT116 CellsHSP70 Heat-Shock ProteinsHumansImmunoprecipitationMicroRNAsMolecular ChaperonesOligonucleotide Array Sequence AnalysisPolyribosomesProtein BiosynthesisReverse Transcriptase Polymerase Chain ReactionRibosomesRNA, MessengerHSP70 Heat-Shock ProteinsMicroRNAsMIRN215 microRNA, humanMolecular ChaperonesRNA, MessengerHSP70miR-215protein chaperonetranslation

Identifiers

PMID26287603
PMCPMC4695198
OpenAlexW1918818207

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.