Evidence map›Paper›PMID 27503895›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2016

miR-579-3p controls melanoma progression and resistance to target therapy.

Luigi Fattore, Rita Mancini, Mario Acunzo, Giulia Romano, Alessandro Laganà, Maria Elena Pisanu, Debora Malpicci, Gabriele Madonna, Domenico Mallardo, Marilena Capone and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 84 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed, 2 pooled it
6.4field-weighted citation impact, top 3% 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

84 citing papers in PubMed, 2 syntheses or guidelines pooled it, 114 citations in OpenAlex.

  1. Pooled it
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  12. A New Approach to Melanoma Treatment: microRNAs.Current topics in medicinal chemistry · 2024
    Review
  13. Article
  14. Review
  15. The new world of RNA diagnostics and therapeutics.Journal of experimental & clinical cancer research : CR · 2023
    Article
  16. Article
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24 more citing papers are in PubMed but not listed here.

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

16 authors at 6 institutions in 3 countries.

Luigi FattoreIstituto Nazionale per lo Studio e la Cura dei Tumori "Fondazione G. Pascale", Naples 80131, Italy;
Rita ManciniDipartimento di Medicina Clinica e Molecolare, Sapienza Università di Roma, Rome 00161, Italy;
Mario AcunzoDepartment of Molecular Virology, Immunology, and Medical Genetics, The Ohio State University Comprehensive Cancer Center, Columbus, OH 43210;
Giulia RomanoDepartment of Molecular Virology, Immunology, and Medical Genetics, The Ohio State University Comprehensive Cancer Center, Columbus, OH 43210;
Alessandro LaganàDepartment of Genetics, Genomic Sciences Icahn School of Medicine at Mount Sinai, New York, NY 10029;
Maria Elena PisanuDipartimento di Medicina Sperimentale e Clinica, Università degli Studi di Catanzaro "Magna Graecia", Catanzaro 88100, Italy;
Debora MalpicciDipartimento di Medicina Sperimentale e Clinica, Università degli Studi di Catanzaro "Magna Graecia", Catanzaro 88100, Italy;
Gabriele MadonnaIstituto Nazionale per lo Studio e la Cura dei Tumori "Fondazione G. Pascale", Naples 80131, Italy;
Domenico MallardoIstituto Nazionale per lo Studio e la Cura dei Tumori "Fondazione G. Pascale", Naples 80131, Italy;
Marilena CaponeIstituto Nazionale per lo Studio e la Cura dei Tumori "Fondazione G. Pascale", Naples 80131, Italy;
Franco FulcinitiIstituto Cantonale di Patologia, Servizio di Citologia Clinica, 6600 Locarno, Switzerland.
Luca MazzucchelliIstituto Cantonale di Patologia, Servizio di Citologia Clinica, 6600 Locarno, Switzerland.
Gerardo BottiIstituto Nazionale per lo Studio e la Cura dei Tumori "Fondazione G. Pascale", Naples 80131, Italy;
Carlo M CroceDepartment of Molecular Virology, Immunology, and Medical Genetics, The Ohio State University Comprehensive Cancer Center, Columbus, OH 43210; carlo.croce@osumc.edu g.ciliberto@istitutotumori.na.it.
Paolo Antonio AsciertoIstituto Nazionale per lo Studio e la Cura dei Tumori "Fondazione G. Pascale", Naples 80131, Italy;
Gennaro CilibertoIstituto Nazionale per lo Studio e la Cura dei Tumori "Fondazione G. Pascale", Naples 80131, Italy; carlo.croce@osumc.edu g.ciliberto@istitutotumori.na.it.
Istituto Nazionale Tumori IRCCS "Fondazione G. Pascale" · ITThe Ohio State University · USIstituto Cantonale di Patologia · CHMagna Graecia University · ITIcahn School of Medicine at Mount Sinai · USSapienza University of Rome · IT

Funding

Cancer Gene Discovery to Identify Targetable TargetsR35CA197706 · NCI · OHIO STATE UNIVERSITY · PI CROCE, CARLO M · 2015 to 2021
$6.4M
NCI NIH HHS R35 CA197706
6 · The paper itself

Abstract

Therapy of melanoma patients harboring activating mutations in the BRAF (V-raf murine sarcoma viral oncogene homolog B1) oncogene with a combination of BRAF and MEK inhibitors is plagued by the development of drug resistance. Mutational events, as well as adaptive mechanisms, contribute to the development of drug resistance. In this context we uncover here the role of a miRNA, miR-579-3p. We first show that low expression of miR-579-3p is a negative prognostic factor correlating with poor survival. Expression levels of miR-579-3p decrease from nevi to stage III/IV melanoma samples and even further in cell lines resistant to BRAF/MEK inhibitors. Mechanistically, we demonstrate that miR-579-3p acts as an oncosuppressor by targeting the 3'UTR of two oncoproteins: BRAF and an E3 ubiquitin protein ligase, MDM2. Moreover miR-579-3p ectopic expression impairs the establishment of drug resistance in human melanoma cells. Finally, miR-579-3p is strongly down-regulated in matched tumor samples from patients before and after the development of resistance to targeted therapies.

Indexed as

Gene Expression Regulation, Neoplastic3' Untranslated RegionsAntineoplastic AgentsBase SequenceBinding SitesCell Line, TumorCell MovementCell ProliferationDisease ProgressionDrug Resistance, NeoplasmHumansIndolesMelanomaMicroRNAsPrognosisProtein Kinase Inhibitors3' Untranslated RegionsAntineoplastic AgentsBRAF protein, humanIndolesMDM2 protein, humanMicroRNAsMIRN579 microRNA, humanProtein Kinase InhibitorsProto-Oncogene Proteins B-rafProto-Oncogene Proteins c-mdm2PyridonesPyrimidinonesSulfonamidestrametinibVemurafenibdrug resistancemelanomamiRNAtargeted therapy

Identifiers

PMID27503895
PMCPMC5003278
OpenAlexW2485296348

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.