Evidence map›Paper›PMID 24204026›Full record

ReviewCancer research2013

Targeting microRNAs in pancreatic cancer: microplayers in the big game.

Sheema Khan, Ansarullah, Deepak Kumar, Meena Jaggi, Subhash C Chauhan

Open access · bronzeAbstract readReview
In one paragraph

Review in Cancer research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

34 citing papers in PubMed, 75 citations in OpenAlex.

  1. Review
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  16. miR-128 induces pancreas cancer cell apoptosis by targeting MDM4.Experimental and therapeutic medicine · 2018
    Article
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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

5 authors at 3 institutions in 1 country.

Sheema KhanAuthors' Affiliations: Department of Pharmaceutical Sciences and Center for Cancer Research, University of Tennessee Health Science Center, Memphis, Tennessee; The Sanford Project, Children Health Research Center, Sanford Research/USD, Sioux Falls, South Dakota; and Cancer Research Laboratory, Department of Biological and Environmental Sciences, University of the District of Columbia, Washington, District of Columbia.
Ansarullah
Deepak Kumar
Meena Jaggi
Subhash C Chauhan
Sanford Research · USUniversity of Tennessee Health Science Center · USUniversity of the District of Columbia · US

Funding

The Impact of PD-1 Inhibition on Immune-Response to ChemoradiotherapyP20GM103548 · NIGMS · SANFORD RESEARCH/USD · PI MISKIMINS, W KEITH · 2012 to 2020
$20.8M
CENTER FOR CANCER BIOLOGY RESEARCHP20RR024219 · NCRR · SANFORD RESEARCH/USD · PI MISKIMINS, W KEITH · 2011 to 2011
$2.3M
Etiology of cervical cancer health disparity in American Indian womenU01CA162106 · NCI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI CHAUHAN, SUBHASH C., JAGGI, MEENA · 2012 to 2016
$1.5M
Aspects of MUC13 Mucin in CancerR01CA142736 · NCI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI CHAUHAN, SUBHASH C. · 2010 to 2013
$1.2M
NCI NIH HHS R01 CA142736NCI NIH HHS U01 CA162106NCI NIH HHS U01 CA162106ANCRR NIH HHS P20 RR024219NIGMS NIH HHS P20 GM103548NIGMS NIH HHS P20GM103548
6 · The paper itself

Abstract

The prognosis of patients with pancreatic cancer is extremely poor, and current systemic therapies result in only marginal survival rates for patients. The era of targeted therapies has offered a new avenue to search for more effective therapeutic strategies. Recently, microRNAs (miRNA) that are small noncoding RNAs (18-24 nucleotides) have been associated with a number of diseases, including cancer. Disruption of miRNAs may have important implications in cancer etiology, diagnosis, and treatment. So far, focus has been on the mechanisms that are involved in translational silencing of their targets to fine tune gene expression. This review summarizes the approach for rational validation of selected candidates that might be involved in pancreatic tumorigenesis, cancer progression, and disease management. Herein, we also focus on the major issues hindering the identification of miRNAs, their linked pathways and recent advances in understanding their role as diagnostic/prognostic biomarkers, and therapeutic tools in dealing with this disease. miRNAs are expected to be robust clinical analytes, valuable for clinical research and biomarker discovery.

Indexed as

AdenocarcinomaAnimalsCell Transformation, NeoplasticGenes, Tumor SuppressorGenetic TherapyHumansMicroRNAsMolecular Targeted TherapyPancreatic NeoplasmsMicroRNAs

Identifiers

PMID24204026
PMCPMC3834190
OpenAlexW1985960583

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.