Evidence map›Paper›PMID 37499114›Full record

ReviewEpigenetics2023

Brain Tumors: Development, Drug Resistance, and Sensitization - An Epigenetic Approach.

Sibaji Sarkar, Tara Deyoung, Hope Ressler, Whitney Chandler

Open access · diamondAbstract readReview
In one paragraph

Review in Epigenetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

9 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Review
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  6. Review
  7. Article
  8. Review
  9. Meta-transfer Learning for Brain Tumor Segmentation: Within and Beyond Glioma.Advances in experimental medicine and biology · 2024
    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

4 authors at 2 institutions in 1 country.

Sibaji SarkarDivision of Biotechnology, Quincy College, Quincy, MA, USA.ORCID 0000-0002-2204-3031
Tara DeyoungDivision of Biotechnology, Quincy College, Quincy, MA, USA.
Hope ResslerDivision of Biology, STEM, MBC College, Wellesley, MA, USA.
Whitney ChandlerDivision of Biology, STEM, MBC College, Wellesley, MA, USA.
Quincy College · USWellesley College · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this article, we describe contrasting developmental aspects of paediatric and adult brain tumours. We hypothesize that the formation of cancer progenitor cells, for both paediatric and adult, could be due to epigenetic events. However, the progression of adult brain tumours selectively involves more mutations compared to paediatric tumours. We further discuss epigenetic switches, comprising both histone modifications and DNA methylation, and how they can differentially regulate transcription and expression of oncogenes and tumour suppressor genes. Next, we summarize the currently available therapies for both types of brain tumours, explaining the merits and failures leading to drug resistance. We analyse different mechanisms of drug resistance and the role of epigenetics in this process. We then provide a rationale for combination therapy, which includes epigenetic drugs. In the end, we postulate a concept which describes how a combination therapy could be initiated. The timing, doses, and order of individual drug regimens will depend on the individual case. This type of combination therapy will be part of a personalized medicine which will differ from patient to patient.

Indexed as

Brain NeoplasmsDNA MethylationAdultChildDrug DevelopmentDrug ResistanceEpigenesis, GeneticHumanscombination therapydevelopment of tumoursDNA methylationdrug resistanceepigenetic switchhistone modificationPediatric and adult brain tumourssensitization

Identifiers

PMID37499114
PMCPMC10376921
OpenAlexW4385298146

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.