Evidence map›Paper›PMID 30021798›Full record

ArticleEMBO molecular medicine2018

miR-205 mediates adaptive resistance to MET inhibition via ERRFI1 targeting and raised EGFR signaling.

Cristina Migliore, Elena Morando, Elena Ghiso, Sergio Anastasi, Vera P Leoni, Maria Apicella, Davide Cora', Anna Sapino, Filippo Pietrantonio, Filippo De Braud and 3 more

Open access · goldAbstract read
In one paragraph

Article in EMBO molecular medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.0field-weighted citation impact, top 12% 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

19 citing papers in PubMed, 28 citations in OpenAlex.

  1. The User's Guide to Amivantamab.Targeted oncology · 2025
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  8. Mig-6 Inhibits Autophagy in HCC Cell Lines by Modulating miR-193a-3p.International journal of medical sciences · 2022
    Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Non-Coding RNAs in Lung Tumor Initiation and Progression.International journal of molecular sciences · 2020
    Review
  15. Review
  16. Review
  17. Review
  18. Article
  19. Receptor Tyrosine Kinase-Targeted Cancer Therapy.International journal of molecular sciences · 2018
    Review
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

13 authors at 4 institutions in 1 country.

Cristina MiglioreDepartment of Oncology, University of Torino, Candiolo, Italy cristina.migliore@unito.it oreste.segatto@ifo.gov.it silvia.giordano@unito.it.ORCID 0000-0003-3722-2814
Elena MorandoCandiolo Cancer Institute, FPO-IRCCS, Candiolo, Italy.
Elena GhisoCandiolo Cancer Institute, FPO-IRCCS, Candiolo, Italy.
Sergio AnastasiUnit of Oncogenomics and Epigenetics, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Vera P LeoniDepartment of Biomedical Sciences, Unit of Oncology and Molecular Pathology, University of Cagliari, Cagliari, Italy.
Maria ApicellaCandiolo Cancer Institute, FPO-IRCCS, Candiolo, Italy.
Davide Cora'Department of Oncology, University of Torino, Candiolo, Italy.
Anna SapinoCandiolo Cancer Institute, FPO-IRCCS, Candiolo, Italy.
Filippo PietrantonioMedical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Filippo De BraudMedical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Amedeo ColumbanoDepartment of Biomedical Sciences, Unit of Oncology and Molecular Pathology, University of Cagliari, Cagliari, Italy.
Oreste SegattoUnit of Oncogenomics and Epigenetics, IRCCS Regina Elena National Cancer Institute, Rome, Italy cristina.migliore@unito.it oreste.segatto@ifo.gov.it silvia.giordano@unito.it.ORCID 0000-0003-2561-1142
Silvia GiordanoDepartment of Oncology, University of Torino, Candiolo, Italy cristina.migliore@unito.it oreste.segatto@ifo.gov.it silvia.giordano@unito.it.ORCID 0000-0003-1854-1086
Candiolo Cancer Institute · ITUniversity of Cagliari · ITUniversity of Milan · ITUniversità degli Studi del Piemonte Orientale “Amedeo Avogadro” · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The onset of secondary resistance represents a major limitation to long-term efficacy of target therapies in cancer patients. Thus, the identification of mechanisms mediating secondary resistance is the key to the rational design of therapeutic strategies for resistant patients. MiRNA profiling combined with RNA-Seq in MET-addicted cancer cell lines led us to identify the miR-205/ERRFI1 (ERBB receptor feedback inhibitor-1) axis as a novel mediator of resistance to MET tyrosine kinase inhibitors (TKIs). In cells resistant to MET-TKIs, epigenetically induced miR-205 expression determined the downregulation of ERRFI1 which, in turn, caused EGFR activation, sustaining resistance to MET-TKIs. Anti-miR-205 transduction reverted crizotinib resistance

Indexed as

Drug ResistanceSignal TransductionAdaptor Proteins, Signal TransducingAntineoplastic AgentsCrizotinibEnzyme InhibitorsErbB ReceptorsGene Expression ProfilingHumansMicroRNAsProto-Oncogene Proteins c-metSequence Analysis, RNATumor Suppressor ProteinsAdaptor Proteins, Signal TransducingAntineoplastic AgentsCrizotinibEGFR protein, humanEnzyme InhibitorsErbB ReceptorsERRFI1 protein, humanMET protein, humanMicroRNAsMIR205, humanProto-Oncogene Proteins c-metTumor Suppressor ProteinsEGFRERRFI1METresistancetargeted therapy

Identifiers

PMID30021798
PMCPMC6127885
OpenAlexW2883817645

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.