Evidence map›Paper›PMID 33922974›Full record

ReviewCancers2021

The Role of Epigenetics in the Progression of Clear Cell Renal Cell Carcinoma and the Basis for Future Epigenetic Treatments.

Javier C Angulo, Claudia Manini, Jose I López, Angel Pueyo, Begoña Colás, Santiago Ropero

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

25 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Effects ofThe Journal of international medical research · 2022
    Article
  18. Article
  19. Article
  20. Article
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 5 institutions in 2 countries.

Javier C AnguloClinical Department, Faculty of Medical Sciences, European University of Madrid, 28005 Madrid, Spain.ORCID 0000-0002-1735-8792
Claudia ManiniDepartment of Pathology, San Giovanni Bosco Hospital, 10154 Turin, Italy.
Jose I LópezDepartment of Pathology, Cruces University Hospital, 48903 Barakaldo, Spain.ORCID 0000-0003-0842-5348
Angel PueyoFoundation for Biomedical Research, Innovation of University Hospitals Infanta Leonor and South-East, 28003 Madrid, Spain.
Begoña ColásBiochemistry and Molecular Biology Unit, Department of Systems Biology, University of Alcalá, 28805 Alcalá de Henares, Spain.
Santiago RoperoBiochemistry and Molecular Biology Unit, Department of Systems Biology, University of Alcalá, 28805 Alcalá de Henares, Spain.
Universidad de Alcalá · ESBioCruces Health research Institute · ESHospital Universitario de Getafe · ESHospital Universitario Infanta Leonor · ESOspedale San Giovanni Bosco · IT

Funding

Instituto de Salud Carlos III PI16/00594Instituto de Salud Carlos III PI19/00213
6 · The paper itself

Abstract

Clear cell renal cell carcinoma (ccRCC) is curable when diagnosed at an early stage, but when disease is non-confined it is the urologic cancer with worst prognosis. Antiangiogenic treatment and immune checkpoint inhibition therapy constitute a very promising combined therapy for advanced and metastatic disease. Many exploratory studies have identified epigenetic markers based on DNA methylation, histone modification, and ncRNA expression that epigenetically regulate gene expression in ccRCC. Additionally, epigenetic modifiers genes have been proposed as promising biomarkers for ccRCC. We review and discuss the current understanding of how epigenetic changes determine the main molecular pathways of ccRCC initiation and progression, and also its clinical implications. Despite the extensive research performed, candidate epigenetic biomarkers are not used in clinical practice for several reasons. However, the accumulated body of evidence of developing epigenetically-based biomarkers will likely allow the identification of ccRCC at a higher risk of progression. That will facilitate the establishment of firmer therapeutic decisions in a changing landscape and also monitor active surveillance in the aging population. What is more, a better knowledge of the activities of chromatin modifiers may serve to develop new therapeutic opportunities. Interesting clinical trials on epigenetic treatments for ccRCC associated with well established antiangiogenic treatments and immune checkpoint inhibitors are revisited.

Indexed as

biomarkerDNA methylationepigeneticsrenal cell carcinoma

Identifiers

PMID33922974
PMCPMC8123355
OpenAlexW3157334871

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.