Evidence map›Paper›PMID 27507554›Full record

ArticleJournal of gastrointestinal surgery : official journal of the Society for Surgery of the Alimentary Tract2017

Restitution of Tumor Suppressor MicroRNA-145 Using Magnetic Nanoformulation for Pancreatic Cancer Therapy.

Saini Setua, Sheema Khan, Murali M Yallapu, Stephen W Behrman, Mohammed Sikander, Shabia Shabir Khan, Meena Jaggi, Subhash C Chauhan

Open access · greenAbstract read
In one paragraph

Article in Journal of gastrointestinal surgery : official journal of the Society for Surgery of the Alimentary Tract, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.6field-weighted citation impact, top 8% 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

29 citing papers in PubMed, 49 citations in OpenAlex.

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  12. COVID-19: fighting the invisible enemy with microRNAs.Expert review of anti-infective therapy · 2021
    Review
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  15. Nanoscale delivery systems for microRNAs in cancer therapy.Cellular and molecular life sciences : CMLS · 2020
    Review
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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 2 countries.

Saini SetuaDepartment of Pharmaceutical Sciences and Center for Cancer Research, University of Tennessee Health Science Center, 19 South Manassas, Cancer Research Building, Memphis, TN, USA.
Sheema KhanDepartment of Pharmaceutical Sciences and Center for Cancer Research, University of Tennessee Health Science Center, 19 South Manassas, Cancer Research Building, Memphis, TN, USA.
Murali M YallapuDepartment of Pharmaceutical Sciences and Center for Cancer Research, University of Tennessee Health Science Center, 19 South Manassas, Cancer Research Building, Memphis, TN, USA.
Stephen W BehrmanDepartment of Surgery, University of Tennessee Health Science Center, Memphis, TN, USA.
Mohammed SikanderDepartment of Pharmaceutical Sciences and Center for Cancer Research, University of Tennessee Health Science Center, 19 South Manassas, Cancer Research Building, Memphis, TN, USA.
Shabia Shabir KhanDepartment of Computer Science, University of Kashmir, Srinagar, Jammu and Kashmir, India.
Meena JaggiDepartment of Pharmaceutical Sciences and Center for Cancer Research, University of Tennessee Health Science Center, 19 South Manassas, Cancer Research Building, Memphis, TN, USA.
Subhash C ChauhanDepartment of Pharmaceutical Sciences and Center for Cancer Research, University of Tennessee Health Science Center, 19 South Manassas, Cancer Research Building, Memphis, TN, USA. schauha1@uthsc.edu.
University of Tennessee Health Science Center · USCenter for Cancer Research · USUniversity of Kashmir · IN

Funding

MUC13 Mucin in Colorectal Cancer Health DisparityR01CA204552 · NCI · UNIVERSITY OF TEXAS RIO GRANDE VALLEY · PI CHAUHAN, SUBHASH C. · 2016 to 2020
$1.7M
Development of Targeted Nanotechnology Platform for Pancreatic CancerR01CA206069 · NCI · UNIVERSITY OF TEXAS RIO GRANDE VALLEY · PI CHAUHAN, SUBHASH C. · 2016 to 2021
$1.7M
Targeted Nanotherapy for Pancreatic CancerR01CA210192 · NCI · UNIVERSITY OF TEXAS RIO GRANDE VALLEY · PI CHAUHAN, SUBHASH C. · 2016 to 2021
$1.7M
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
PSMA Targeted Docetaxel Loaded Magnetic Nanoparticles for Prostate Cancer TherapyK22CA174841 · NCI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI YALLAPU, MURALI MOHAN · 2015 to 2017
$485k
NCI NIH HHS K22 CA174841NCI NIH HHS R01 CA142736NCI NIH HHS R01 CA204552NCI NIH HHS R01 CA206069NCI NIH HHS R01 CA210192NCI NIH HHS U01 CA162106
6 · The paper itself

Abstract

introductionThe functional significance of lost microRNAs has been reported in several human malignancies, including pancreatic cancer (PC). Our prior work has identified microRNA-145 (miR-145) as a tumor suppressor microRNA (miRNA) in pancreatic cancer. The restoration of miR-145 downregulates a number of oncogenes including mucin MUC13, a transmembrane glycoprotein that is aberrantly expressed in pancreatic cancer, thus efficiently inhibiting tumor growth in mice. However, lack of an effective tumor-specific delivery system remains an unmet clinical challenge for successful translation of microRNAs.

methodsWe developed a miRNA-145-based magnetic nanoparticle formulation (miR-145-MNPF) and assessed its anti-cancer efficacy. Physico-chemical characterization (dynamic light scattering (DLS), transmission electron microscopy (TEM) and miR-binding efficiency), cellular internalization (Prussian blue and confocal microscopy), miR-145 restitution potential (quantitative reverse-transcription PCR (qRT-PCR), and anti-cancer efficacy (proliferation, colony formation, cell migration, cell invasion assays) of this formulation were performed using clinically relevant pancreatic cancer cell lines (HPAF-II, AsPC-1).

resultsmiR-145-MNPF exhibited optimal particle size and zeta potential which effectively internalized and restituted miR-145 in pancreatic cancer cells. miR-145 re-expression resulted in downregulation of MUC13, HER2, pAKT, and inhibition of cell proliferation, clonogenicity, migration, and invasion of pancreatic cancer cells.

conclusionsmiR-145-MNPF is an efficient system for miR-145 delivery and restitution in pancreas cancer that may offer a potential therapeutic treatment for PC either alone or in conjunction with conventional treatment.

Indexed as

Cell Line, TumorCell MovementCell ProliferationDown-RegulationGene Expression Regulation, NeoplasticGenetic TherapyHumansMagnetite NanoparticlesMicroRNAsMucinsPancreatic NeoplasmsReal-Time Polymerase Chain ReactionMagnetite NanoparticlesMicroRNAsMUC13 protein, humanMucinsMagnetic nanoparticlemiR-145NanotherapiesPancreatic cancerTherapeutics

Identifiers

PMID27507554
PMCPMC5336381
OpenAlexW2526190858

What OpenQuestion holds

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Registered trials

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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.