Evidence map›Paper›PMID 28748501›Full record

ReviewCellular oncology (Dordrecht, Netherlands)2017

A step-by-step microRNA guide to cancer development and metastasis.

Georgios S Markopoulos, Eugenia Roupakia, Maria Tokamani, Evangelia Chavdoula, Maria Hatziapostolou, Christos Polytarchou, Kenneth B Marcu, Athanasios G Papavassiliou, Raphael Sandaltzopoulos, Evangelos Kolettas

Abstract readReview
In one paragraph

Review in Cellular oncology (Dordrecht, Netherlands), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 104 papers.

0numbers the graph read from it
0cells of the map it votes in
104citing papers in PubMed
7.3field-weighted citation impact, top 1% 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

104 citing papers in PubMed, 172 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Identification of Oncogene-Induced Senescence-Associated MicroRNAs.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  7. Review
  8. Article
  9. Topology and Dynamics of Transcriptome (Dys)Regulation.International journal of molecular sciences · 2024
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Value of negatively correlated miR-205-5p/Cancer pathogenesis and therapy · 2023
    Article
  20. Article

44 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

10 authors at 5 institutions in 4 countries.

Georgios S MarkopoulosLaboratory of Biology, School of Medicine, Faculty of Health Sciences, University of Ioannina, 45110, Ioannina, Greece.
Eugenia RoupakiaLaboratory of Biology, School of Medicine, Faculty of Health Sciences, University of Ioannina, 45110, Ioannina, Greece.
Maria TokamaniDepartment of Molecular Biology and Genetics, Democritus University of Thrace, 68100, Alexandroupolis, Greece.
Evangelia ChavdoulaLaboratory of Biology, School of Medicine, Faculty of Health Sciences, University of Ioannina, 45110, Ioannina, Greece.
Maria HatziapostolouDepartment of Biosciences, School of Science and Technology, Nottingham Trent University, Nottingham, MG11 8NS, UK.
Christos PolytarchouDepartment of Biosciences, School of Science and Technology, Nottingham Trent University, Nottingham, MG11 8NS, UK.
Kenneth B MarcuBiomedical Research Division, Institute of Molecular Biology and Biotechnology, Foundation for Research and Technology, 45110, Ioannina, Greece.
Athanasios G PapavassiliouDepartment of Biological Chemistry, Medical School, National and Kapodistrian University of Athens, 75 M. Asias Street, 11527, Athens, Greece.
Raphael SandaltzopoulosDepartment of Molecular Biology and Genetics, Democritus University of Thrace, 68100, Alexandroupolis, Greece.
Evangelos KolettasLaboratory of Biology, School of Medicine, Faculty of Health Sciences, University of Ioannina, 45110, Ioannina, Greece. ekoletas@cc.uoi.gr.ORCID http://orcid.org/0000-0002-5820-487X
University of Ioannina · GRDemocritus University of Thrace · GRNottingham Trent University · GBAcademy of Athens · GRNational and Kapodistrian University of Athens · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCancer is one of the leading causes of mortality. The neoplastic transformation of normal cells to cancer cells is caused by a progressive accumulation of genetic and epigenetic alterations in oncogenes, tumor suppressor genes and epigenetic regulators, providing cells with new properties, collectively known as the hallmarks of cancer. During the process of neoplastic transformation cells progressively acquire novel characteristics such as unlimited growth potential, increased motility and the ability to migrate and invade adjacent tissues, the ability to spread from the tumor of origin to distant sites, and increased resistance to various types of stresses, mostly attributed to the activation of genetic stress-response programs. Accumulating evidence indicates a crucial role of microRNAs (miRNAs or miRs) in the initiation and progression of cancer, acting either as oncogenes (oncomirs) or as tumor suppressors via several molecular mechanisms. MiRNAs comprise a class of small ~22 bp long noncoding RNAs that play a key role in the regulation of gene expression at the post-transcriptional level, acting as negative regulators of mRNA translation and/or stability. MiRNAs are involved in the regulation of a variety of biological processes including cell cycle progression, DNA damage responses and apoptosis, epithelial-to-mesenchymal cell transitions, cell motility and stemness through complex and interactive transcription factor-miRNA regulatory networks.

conclusionsThe impact and the dynamic potential of miRNAs with oncogenic or tumor suppressor properties in each stage of the multistep process of tumorigenesis, and in the adaptation of cancer cells to stress, are discussed. We propose that the balance between oncogenic versus tumor suppressive miRNAs acting within transcription factor-miRNA regulatory networks, influences both the multistage process of neoplastic transformation, whereby normal cells become cancerous, and their stress responses. The role of specific tumor-derived exosomes containing miRNAs and their use as biomarkers in diagnosis and prognosis, and as therapeutic targets, are also discussed.

Indexed as

CarcinogenesisCell Transformation, NeoplasticDisease ProgressionEpithelial-Mesenchymal TransitionGene Expression Regulation, NeoplasticGenes, Tumor SuppressorHumansMicroRNAsNeoplasmsPrognosisMicroRNAsBiomarkersCancerEpithelial-to mesenchymal cell transition (EMT)ExosomesMicroRNAs (miRNAs or miRs)Stages of tumorigenesisTranscription factor-miRNA regulatory networks

Identifiers

PMID28748501
PMCPMC13001585
OpenAlexW2736691269

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.