Evidence map›Paper›PMID 27569217›Full record

ArticleCancer research2016

Deep Sequencing Reveals a Novel miR-22 Regulatory Network with Therapeutic Potential in Rhabdomyosarcoma.

Francesca Bersani, Marcello Francesco Lingua, Deborah Morena, Valentina Foglizzo, Silvia Miretti, Letizia Lanzetti, Giovanna Carrà, Alessandro Morotti, Ugo Ala, Paolo Provero and 6 more

Open access · greenAbstract read
In one paragraph

Article in Cancer research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

24 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. A dysfunctional miR-1-TRPS1-MYOG axis drives ERMS by suppressing terminal myogenic differentiation.Molecular therapy : the journal of the American Society of Gene Therapy · 2023
    Article
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  11. Review
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  15. Article
  16. Article
  17. miRNA signatures in childhood sarcomas and their clinical implications.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2019
    Review
  18. MiRNAs as Players in Rhabdomyosarcoma Development.International journal of molecular sciences · 2019
    Review
  19. Article
  20. Non-Coding RNAs in Pediatric Solid Tumors.Frontiers in genetics · 2019
    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

16 authors at 1 institution in 1 country.

Francesca BersaniDepartment of Oncology, University of Turin, Orbassano, Turin, Italy. CeRMS, Center for Experimental Research and Medical Studies, Turin, Italy.
Marcello Francesco LinguaDepartment of Oncology, University of Turin, Orbassano, Turin, Italy. CeRMS, Center for Experimental Research and Medical Studies, Turin, Italy.
Deborah MorenaDepartment of Oncology, University of Turin, Orbassano, Turin, Italy. CeRMS, Center for Experimental Research and Medical Studies, Turin, Italy.
Valentina FoglizzoDepartment of Oncology, University of Turin, Orbassano, Turin, Italy. CeRMS, Center for Experimental Research and Medical Studies, Turin, Italy.
Silvia MirettiDepartment of Veterinary Science, University of Turin, Grugliasco, Italy.
Letizia LanzettiDepartment of Oncology, University of Turin, Orbassano, Turin, Italy. Candiolo Cancer Institute, Candiolo, Turin, Italy.
Giovanna CarràDepartment of Clinical and Biological Sciences, University of Turin, Orbassano, Italy.
Alessandro MorottiDepartment of Clinical and Biological Sciences, University of Turin, Orbassano, Italy.
Ugo AlaDepartment of Molecular Biotechnology and Health Sciences, University of Turin, Turin, Italy.
Paolo ProveroDepartment of Molecular Biotechnology and Health Sciences, University of Turin, Turin, Italy.
Roberto ChiarleCeRMS, Center for Experimental Research and Medical Studies, Turin, Italy. Department of Molecular Biotechnology and Health Sciences, University of Turin, Turin, Italy. Department of Pathology, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts.
Samuel SingerDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York.
Marc LadanyiDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Thomas TuschlDepartment of RNA Molecular Biology, Howard Hughes Medical Institute, The Rockefeller University, New York, New York.
Carola PonzettoDepartment of Oncology, University of Turin, Orbassano, Turin, Italy. CeRMS, Center for Experimental Research and Medical Studies, Turin, Italy. riccardo.taulli@unito.it carola.ponzetto@unito.it.
Riccardo TaulliDepartment of Oncology, University of Turin, Orbassano, Turin, Italy. CeRMS, Center for Experimental Research and Medical Studies, Turin, Italy. riccardo.taulli@unito.it carola.ponzetto@unito.it.
University of Turin · IT

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
SPORE in Soft Tissue SarcomaP50CA140146 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI SPRIGGS, DAVID R · 2010 to 2014
$11.1M
NCI NIH HHS P30 CA008748NCI NIH HHS P50 CA140146
6 · The paper itself

Abstract

Current therapeutic options for the pediatric cancer rhabdomyosarcoma have not improved significantly, especially for metastatic rhabdomyosarcoma. In the current work, we performed a deep miRNA profiling of the three major human rhabdomyosarcoma subtypes, along with cell lines and normal muscle, to identify novel molecular circuits with therapeutic potential. The signature we determined could discriminate rhabdomyosarcoma from muscle, revealing a subset of muscle-enriched miRNA (myomiR), including miR-22, which was strongly underexpressed in tumors. miR-22 was physiologically induced during normal myogenic differentiation and was transcriptionally regulated by MyoD, confirming its identity as a myomiR. Once introduced into rhabdomyosarcoma cells, miR-22 decreased cell proliferation, anchorage-independent growth, invasiveness, and promoted apoptosis. Moreover, restoring miR-22 expression blocked tumor growth and prevented tumor dissemination in vivo Gene expression profiling analysis of miR-22-expressing cells suggested TACC1 and RAB5B as possible direct miR-22 targets. Accordingly, loss- and gain-of-function experiments defined the biological relevance of these genes in rhabdomyosarcoma pathogenesis. Finally, we demonstrated the ability of miR-22 to intercept and overcome the intrinsic resistance to MEK inhibition based on ERBB3 upregulation. Overall, our results identified a novel miR-22 regulatory network with critical therapeutic implications in rhabdomyosarcoma. Cancer Res; 76(20); 6095-106. ©2016 AACR.

Indexed as

Gene Regulatory NetworksHigh-Throughput Nucleotide SequencingAnimalsCell DifferentiationCell Line, TumorFemaleFetal ProteinsGene Expression Regulation, NeoplasticHumansMiceMicroRNAsMicrotubule-Associated ProteinsMitogen-Activated Protein Kinase KinasesMyoD ProteinNuclear ProteinsPromoter Regions, GeneticERBB3 protein, humanFetal ProteinsMicroRNAsMicrotubule-Associated ProteinsMIRN22 microRNA, humanMIRN378 microRNA, humanMitogen-Activated Protein Kinase KinasesMyoD ProteinNuclear ProteinsRAB5C protein, humanrab5 GTP-Binding ProteinsReceptor, ErbB-3TACC1 protein, human

Identifiers

PMID27569217
PMCPMC5207039
OpenAlexW2515668690

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.