Evidence map›Paper›PMID 30322013›Full record

ArticleCancers2018

Targeting MicroRNA-143 Leads to Inhibition of Glioblastoma Tumor Progression.

Eunice L Lozada-Delgado, Nilmary Grafals-Ruiz, Miguel A Miranda-Román, Yasmarie Santana-Rivera, Fatma Valiyeva, Mónica Rivera-Díaz, María J Marcos-Martínez, Pablo E Vivas-Mejía

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

14 citing papers in PubMed, 29 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

8 authors at 3 institutions in 1 country.

Eunice L Lozada-DelgadoDepartment of Biology, Rio Piedras Campus, University of Puerto Rico, San Juan, PR 00931, USA. eunice.lozada@upr.edu.ORCID 0000-0001-8971-4314
Nilmary Grafals-RuizComprehensive Cancer Center, University of Puerto Rico, San Juan, PR 00935, USA. nilmary.grafals1@upr.edu.
Miguel A Miranda-RománDepartment of Biology, Rio Piedras Campus, University of Puerto Rico, San Juan, PR 00931, USA. mirandar.miguel@gmail.com.ORCID 0000-0003-4914-848X
Yasmarie Santana-RiveraDepartment of Biology, Rio Piedras Campus, University of Puerto Rico, San Juan, PR 00931, USA. yasmarie.santana@upr.edu.
Fatma ValiyevaComprehensive Cancer Center, University of Puerto Rico, San Juan, PR 00935, USA. fvaliyeva@cccupr.org.
Mónica Rivera-DíazDepartment of Biochemistry, Medical Sciences Campus, University of Puerto Rico, San Juan, PR 00936, USA. mrivera@bromediconllc.com.
María J Marcos-MartínezDepartment of Pathology and Laboratory Medicine, Medical Sciences Campus, University of Puerto Rico, San Juan, PR 00936, USA. maria.marcos@upr.edu.
Pablo E Vivas-MejíaDepartment of Biochemistry, Medical Sciences Campus, University of Puerto Rico, San Juan, PR 00936, USA. pablo.vivas@upr.edu.
University of Puerto Rico, Medical Sciences Campus · PRUniversity of Puerto Rico at Río Piedras · PRUniversity of Puerto Rico System · PR

Funding

Upstream Regulation and Downstream effectors of c-MYC in Ovarian CancerU54MD007600 · NIMHD · UNIVERSITY OF PUERTO RICO MED SCIENCES · PI Abiel Roche-Lima · 2017 to 2026
$35.8M
RISE Option III: MBRS RISE at the UPR Medical Sciences CampusR25GM061838 · NIGMS · UNIVERSITY OF PUERTO RICO MED SCIENCES · PI CADILLA, CARMEN LYDIA · 2000 to 2021
$25.5M
National Institute on Minority Health and Health Disparities U54 MD007600National Institutes of Health R25-GM061838NIGMS NIH HHS R25 GM061838NIMHD NIH HHS U54 MD007600
6 · The paper itself

Abstract

Glioblastoma (GBM) is the most common and aggressive of all brain tumors, with a median survival of only 14 months after initial diagnosis. Novel therapeutic approaches are an unmet need for GBM treatment. MicroRNAs (miRNAs) are a class of small non-coding RNAs that regulate gene expression at the post-transcriptional level. Several dysregulated miRNAs have been identified in all cancer types including GBM. In this study, we aimed to uncover the role of miR-143 in GBM cell lines, patient samples, and mouse models. Quantitative real-time RT-PCR of RNA extracted from formalin-fixed paraffin-embedded (FFPE) samples showed that the relative expression of miR-143 was higher in GBM patients compared to control individuals. Transient transfection of GBM cells with a miR-143 oligonucleotide inhibitor (miR-143-inh) resulted in reduced cell proliferation, increased apoptosis, and cell cycle arrest. SLC30A8, a glucose metabolism-related protein, was identified as a direct target of miR-143 in GBM cells. Moreover, multiple injections of GBM tumor-bearing mice with a miR-143-inh-liposomal formulation significantly reduced tumor growth compared to control mice. The reduced in vitro cell growth and in vivo tumor growth following miRNA-143 inhibition suggests that miR-143 is a potential therapeutic target for GBM therapy.

Indexed as

cell proliferationglioblastomamicroRNAsmouse model

Identifiers

PMID30322013
PMCPMC6210372
OpenAlexW2897361396

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.