Evidence map›Paper›PMID 27094812›Full record

ReviewJournal of molecular medicine (Berlin, Germany)2016

miR-200c: a versatile watchdog in cancer progression, EMT, and drug resistance.

Merve Mutlu, Umar Raza, Özge Saatci, Erol Eyüpoğlu, Emre Yurdusev, Özgür Şahin

Open access · bronzeAbstract readReview
PubMed Publisher
In one paragraph

Review in Journal of molecular medicine (Berlin, Germany), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 87 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
87citing papers in PubMed, 2 pooled it
6.2field-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

87 citing papers in PubMed, 2 syntheses or guidelines pooled it, 139 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  12. Regulatory Effects ofFood science & nutrition · 2025
    Article
  13. Review
  14. Article
  15. Article
  16. Review
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  18. MicroRNA-200c in Cancer Generation, Invasion, and Metastasis.International journal of molecular sciences · 2025
    Review
  19. Article
  20. Article

27 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

6 authors at 1 institution in 1 country.

Merve MutluDepartment of Molecular Biology and Genetics, Faculty of Science, Bilkent University, B Building SB-247, 06800, Ankara, Turkey.
Umar RazaDepartment of Molecular Biology and Genetics, Faculty of Science, Bilkent University, B Building SB-247, 06800, Ankara, Turkey.
Özge SaatciDepartment of Molecular Biology and Genetics, Faculty of Science, Bilkent University, B Building SB-247, 06800, Ankara, Turkey.
Erol EyüpoğluDepartment of Molecular Biology and Genetics, Faculty of Science, Bilkent University, B Building SB-247, 06800, Ankara, Turkey.
Emre YurdusevDepartment of Molecular Biology and Genetics, Faculty of Science, Bilkent University, B Building SB-247, 06800, Ankara, Turkey.
Özgür ŞahinDepartment of Molecular Biology and Genetics, Faculty of Science, Bilkent University, B Building SB-247, 06800, Ankara, Turkey. sahinozgur@gmail.com.
Bilkent University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs (miRNAs) are 20-22-nucleotide small endogenous non-coding RNAs which regulate gene expression at post-transcriptional level. In the last two decades, identification of almost 2600 miRNAs in human and their potential to be modulated opened a new avenue to target almost all hallmarks of cancer. miRNAs have been classified as tumor suppressors or oncogenes depending on the phenotype they induce, the targets they modulate, and the tissue where they function. miR-200c, an illustrious tumor suppressor, is one of the highly studied miRNAs in terms of development, stemness, proliferation, epithelial-mesenchymal transition (EMT), therapy resistance, and metastasis. In this review, we first focus on the regulation of miR-200c expression and its role in regulating EMT in a ZEB1/E-cadherin axis-dependent and ZEB1/E-cadherin axis-independent manner. We then describe the role of miR-200c in therapy resistance in terms of multidrug resistance, chemoresistance, targeted therapy resistance, and radiotherapy resistance in various cancer types. We highlight the importance of miR-200c at the intersection of EMT and chemoresistance. Furthermore, we show how miR-200c coordinates several important signaling cascades such as TGF-β signaling, PI3K/Akt signaling, Notch signaling, VEGF signaling, and NF-κB signaling. Finally, we discuss miR-200c as a potential prognostic/diagnostic biomarker in several diseases, but mainly focusing on cancer and its potential application in future therapeutics.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsAntigens, CDAntineoplastic AgentsCadherinsCell Transformation, NeoplasticDisease ProgressionDrug Resistance, NeoplasmEpithelial-Mesenchymal TransitionHumansMicroRNAsNeoplasmsSignal TransductionTransforming Growth Factor betaZinc Finger E-box-Binding Homeobox 1Zinc Finger E-box Binding Homeobox 2Antigens, CDAntineoplastic AgentsCadherinsCDH1 protein, humanMicroRNAsMIRN200 microRNA, humanTransforming Growth Factor betaZEB1 protein, humanZEB2 protein, humanZinc Finger E-box-Binding Homeobox 1Zinc Finger E-box Binding Homeobox 2BiomarkerCell signalingDrug resistanceEpithelial-mesenchymal transition (EMT)miR-200cTGF-βZEB1/2

Identifiers

PMID27094812
OpenAlexW2339549122

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.